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Progress in Lipid Research (78)
References
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443
10.1016/j.bbalip.2012.08.007
/ Biochim Biophys Acta / A retrospective: use of Escherichia coli as a vehicle to study phospholipid synthesis and function by Dowhan (2012)10.1016/S0163-7827(02)00007-3
/ Prog Lipid Res / Multi-subunit acetyl-CoA carboxylases by Cronan (2002)10.1074/jbc.M302507200
/ J Biol Chem / The biotin carboxylase-biotin carboxyl carrier protein complex of Escherichia coli acetyl-CoA carboxylase by Choi-Rhee (2003)10.1016/S0021-9258(18)41860-1
/ J Biol Chem / The genes encoding the two carboxyltransferase subunits of Escherichia coli acetyl-CoA carboxylase by Li (1992)10.1038/nrmicro1839
/ Nat Rev Microbiol / Membrane lipid homeostasis in bacteria by Zhang (2008)10.1016/S0021-9258(19)50498-7
/ J Biol Chem / Isolation and characterization of the β-ketoacyl-acyl carrier protein synthase III gene (fabH) from Escherichia coli K-12 by Tsay (1992)10.1074/jbc.271.18.10996
/ J Biol Chem / Inhibition of β-ketoacyl-acyl carrier protein synthase III (FabH) by acyl-acyl carrier protein in Escherichia coli by Heath (1996)10.1016/j.chembiol.2007.03.013
/ Chem Biol / Alkyl-CoA disulfides as inhibitors and mechanistic probes for FabH enzymes by Alhamadsheh (2007)10.1074/jbc.M311584200
/ J Biol Chem / Expression of two Escherichia coli acetyl-CoA carboxylase subunits is autoregulated by James (2004)10.1128/JB.06309-11
/ J Bacteriol / Dimerization of the bacterial biotin carboxylase subunit is required for acetyl coenzyme A carboxylase activity in vivo by Smith (2012)10.1128/JB.183.4.1499-1503.2001
/ J Bacteriol / Inhibition of Escherichia coli acetyl coenzyme A carboxylase by acyl-acyl carrier protein by Davis (2001)10.1016/S0021-9258(19)42203-5
/ J Biol Chem / Acetyl coenzyme A carboxylase system of Escherichia coli. Purification and proterties of the biotin carboxylase, carboxyltransferase, and carboxyl carrier protein components by Gucchait (1974)10.1073/pnas.68.7.1512
/ Proc Natl Acad Sci USA / Acetyl CoA carboxylase: isolation and characterization of native biotin carboxyl carrier protein by Fall (1971)10.1073/pnas.0806873105
/ Proc Natl Acad Sci USA / Andrimid producers encode an acetyl-CoA carboxyltransferase subunit resistant to the action of the antibiotic by Liu (2008)10.1074/jbc.M104102200
/ J Biol Chem / Function of Escherichia coli biotin carboxylase requires catalytic activity of both subunits of the homodimer by Janiyani (2001)10.1016/0005-2760(76)90022-9
/ Biochim Biophys Acta / Stabilization of an acetyl-CoA carboxylase comples from Pseudomonas citronellolis by Fall (1976)10.1111/j.1365-2958.2005.04951.x
/ Mol Microbiol / Transcriptional regulation of fatty acid biosynthesis in Streptococcus pneumoniae by Lu (2006)10.1074/jbc.M004756200
/ J Biol Chem / Overproduction of acetyl-CoA carboxylase activity increases the rate of fatty acid biosynthesis in Escherichia coli by Davis (2000)10.1074/jbc.M101769200
/ J Biol Chem / Identification, substrate specificity, and inhibition of the Streptococcus pneumoniae β-ketoacyl-acyl carrier protein synthase III (FabH) by Khandekar (2001)10.1128/JB.182.2.365-370.2000
/ J Bacteriol / β-Ketoacyl-acyl carrier protein synthase III (FabH) is a determining factor in branched-chain fatty acid biosynthesis by Choi (2000)10.1110/ps.051501605
/ Protein Sci / Crystal structure and substrate specificity of the β-ketoacyl-acyl carrier protein synthase III (FabH) from Staphylococcus aureus by Qiu (2005)10.1016/S0021-9258(18)83280-X
/ J Biol Chem / Acetoacetyl-acyl carrier protein synthase: a target for the antibiotic thiolactomycin by Jackowski (1989)10.1074/jbc.M500964200
/ J Biol Chem / A phosphoethanolamine transferase specific for the outer 3-deoxy-d-manno-octulosonic acid residue of Escherichia coli lipopolysaccharide. Identification of the eptB gene and Ca2+ hypersensitivity of an eptB deletion mutant by Reynolds (2005)10.1128/AAC.46.5.1310-1318.2002
/ Antimicrob Agents Chemother / Purification, characterization, and identification of novel inhibitors of the β-ketoacyl-acyl carrier protein synthase III (FabH) from Staphylococcus aureus by He (2002)10.1006/jmbi.2000.4457
/ J Mol Biol / Refined structures of β-ketoacyl-acyl carrier protein synthase III by Qiu (2001)10.1074/jbc.274.51.36465
/ J Biol Chem / Crystal structure of β-ketoacyl-acyl carrier protein synthase III. A key condensing enzyme in bacterial fatty acid biosynthesis by Qiu (1999)10.1128/JB.187.11.3795-3799.2005
/ J Bacteriol / Alteration of the fatty acid profile of Streptomyces coelicolor by replacement of the initiation enzyme 3-ketoacyl acyl carrier protein synthase III (FabH) by Li (2005)10.1074/jbc.M010762200
/ J Biol Chem / Crystal structure of the Mycobacterium tuberculosis β-ketoacyl-acyl carrier protein synthase III by Scarsdale (2001)10.1074/jbc.M802169200
/ J Biol Chem / A novel interaction linking the FAS-II and phthiocerol dimycocerosate (PDIM) biosynthetic pathways by Kruh (2008)10.1016/S0969-2126(00)00094-0
/ Structure / The 1.8Å cystal structure and active site architecture of β-ketoacyl-[acyl carrier protein] synthase III (FabH) from Escherichia coli by Davies (2000)10.1128/JB.00792-12
/ J Bacteriol / Fatty acid biosynthesis in Pseudomonas aeruginosa is initiated by FabY: a new class of β-ketoacyl-acyl carrier protein synthases by Yuan (2012)10.1074/jbc.M308638200
/ J Biol Chem / β-Ketoacyl-acyl carrier protein synthase III (FabH) is essential for bacterial fatty acid synthesis by Lai (2003)10.1073/pnas.1209742109
/ Proc Natl Acad Sci USA / Regulation of cell size in response to nutrient availability by fatty acid biosynthesis in Escherichia coli by Yao (2012)10.1371/journal.pone.0023479
/ PLoS ONE / The RelA/SpoT homolog (RSH) superfamily: distribution and functional evolution of ppGpp synthetases and hydrolases across the tree of life by Atkinson (2011)10.1073/pnas.90.23.11004
/ Proc Natl Acad Sci USA / SpoT-dependent accumulation of guanosine tetraphosphate in response to fatty acid starvation in Escherichia coli by Seyfzadeh (1993)10.1002/pmic.200500115
/ Proteomics / A protein network for phospholipid synthesis uncovered by a variant of the tandem affinity purification method in Escherichia coli by Gully (2005)10.1111/j.1365-2958.2006.05442.x
/ Mol Microbiol / Acyl carrier protein/SpoT interaction, the switch linking SpoT-dependent stress response to fatty acid metabolism by Battesti (2006)10.1128/JB.01195-08
/ J Bacteriol / Bacteria possessing two RelA/SpoT-Like proteins have evolved a specific stringent response involving the acyl carrier protein-SpoT interaction by Battesti (2009)10.1007/s00203-008-0390-6
/ Arch Microbiol / The Lactococcus lactis FabF fatty acid synthetic enzyme can functionally replace both the FabB and FabF proteins of Escherichia coli and the FabH protein of Lactococcus lactis by Morgan-Kiss (2008)10.1016/S0021-9258(19)45231-9
/ J Biol Chem / Acyl carrier protein. XV. Studies of β-ketoacyl-acyl carrier protein synthetase by Alberts (1972)10.1016/S1874-6047(08)60037-2
/ The enzymes / Acyl-CoA carboxylases by Alberts (1972)10.1042/bst0280607
/ Biochem Soc Trans / Acyl carrier protein (ACP) inhibition and other differences between β-ketoacyl synthase (KAS) I and II by Arnvig (2000)10.1074/jbc.271.44.27795
/ J Biol Chem / Roles of the FabA and FabZ β-hydroxyacyl-acyl carrier protein dehydratases in Escherichia coli fatty acid biosynthesis by Heath (1996)10.1016/S0969-2126(00)00115-5
/ Structure / The X-ray structure of Brassica napus β-ketoacyl carrier protein reductase and its implications for substrate binding and catalysis by Fisher (2000)10.1021/bi010737g
/ Biochemistry / The structure of β-ketoacyl-[acyl carrier protein] reductase from Escherichia coli: negative cooperativity and its structural basis by Price (2001)10.1016/S0022-2836(02)00463-1
/ J Mol Biol / Crystal structure of MabA from Mycobacterium tuberculosis, a reductase involved in long-chain fatty acid biosynthesis by Cohen-Gonsaud (2002)10.1128/JB.143.2.726-730.1980
/ J Bacteriol / Regulation of fatty acid degradation in Escherichia coli: dominance studies with strains merodiploid in gene fadR by Simons (1980)10.1074/jbc.270.44.26538
/ J Biol Chem / Enoyl-acyl carrier protein reductase (fabI) plays a determinant role in completing cycles of fatty acid elongation in Escherichia coli by Heath (1995)10.1042/bj3091029
/ Biochem J / Enoyl-acyl-carrier-protein reductase and Mycobacterium tuberculosis InhA do not conserve the Tyr-Xaa-Xaa-Xaa-Lys motif in mammalian 11β- and 17β-hydroxysteroid dehydrogenases and Drosophila alcohol dehydrogenase by Baker (1995)10.1074/jbc.M005611200
/ J Biol Chem / The enoyl-[acyl-carrier-protein] reductases FabI and FabL from Bacillus subtilis by Heath (2000)10.1074/jbc.M708171200
/ J Biol Chem / Vibrio cholerae fabV defines a new class of enoyl acyl-carrier-protein reductase by Massengo-Tiasse (2008)10.1128/AAC.01152-09
/ Antimicrob Agents Chemother / Triclosan resistance of Pseudomonas aeruginosa PAO1 is due to FabV, a triclosan-resistant enoyl-acyl carrier protein reductase by Zhu (2010)10.1021/bi902001a
/ Biochemistry / Mechanism and inhibition of the FabV enoyl-ACP reductase from Burkholderia mallei by Lu (2010)10.1016/j.chembiol.2010.07.015
/ Chem Biol / The kalimantacin/batumin biosynthesis operon encodes a self-resistance isoform of the FabI bacterial target by Mattheus (2010)10.1016/j.str.2011.07.019
/ Structure / Structure of the Yersinia pestis FabV enoyl-ACP reductase and its interaction with two 2-pyridone inhibitors by Hirschbeck (2012)10.1371/journal.pone.0026743
/ PLoS ONE / Determination of the crystal structure and active residues of FabV, the enoyl-ACP reductase from Xanthomonas oryzae by Li (2011)10.1038/35022656
/ Nature (London) / A triclosan-resistant bacterial enzyme by Heath (2000)10.1110/ps.073288808
/ Protein Sci / Crystal structure of enoyl-acyl carrier protein reductase (FabK) from Streptococcus pneumoniae reveals the binding mode of an inhibitor by Saito (2008)10.1074/jbc.272.29.17903
/ J Biol Chem / A new metabolic link; the acyl carrier protein of lipid synthesis donates lipoic acid to the pyruvate dehydrogenase complex in Escherichia coli and mitochondria by Jordan (1997)10.1021/bi051865y
/ Biochemistry / The reaction of LipB, the octanoyl-[acyl carrier protein]:protein N-octanoyltransferase of lipoic acid synthesis, proceeds through an acyl-enzyme intermediate by Zhao (2005)10.1128/jb.175.5.1325-1336.1993
/ J Bacteriol / Lipoic acid metabolism in Escherichia coli: sequencing and functional characterization of the lipA and lipB genes by Reed (1993)10.1038/nchembio.420
/ Nat Chem Biol / Biotin synthesis begins by hijacking the fatty acid synthetic pathway by Lin (2010)10.1146/annurev.biochem.76.010307.145803
/ Annu Rev Biochem / Lipid A modification systems in Gram-negative bacteria by Raetz (2007)10.1073/pnas.1109208108
/ Proc Natl Acad Sci USA / Metabolic basis for the differential susceptibility of Gram-positive pathogens to fatty acid synthesis inhibitors by Parsons (2011)10.1126/science.272.5268.1655
/ Science / Enzymatic synthesis of a quorum-sensing autoinducer through use of defined substrates by More (1996)10.1128/JB.180.10.2644-2651.1998
/ J Bacteriol / In vivo evidence that S-adenosylmethionine and fatty acid synthesis intermediates are the substrates for the LuxI family of autoinducer synthases by Val (1998)10.1128/JB.187.11.3630-3635.2005
/ J Bacteriol / Biosynthetic pathway of Pseudomonas aeruginosa 4-hydroxy-2-alkylquinolines by Bredenbruch (2005)10.1128/JB.00080-08
/ J Bacteriol / RhlA converts β-hydroxyacyl-acyl carrier protein intermediates in fatty acid synthesis to the β-hydroxydecanoyl-β-hydroxydecanoate component of rhamnolipids in Pseudomonas aeruginosa by Zhu (2008)10.1111/j.1365-2958.2012.07968.x
/ Mol Microbiol / The Burkholderia cenocepacia BDSF quorum sensing fatty acid is synthesized by a bifunctional crotonase homologue having both dehydratase and thioesterase activities by Bi (2012)10.1016/S0021-9258(19)44280-4
/ J Biol Chem / An estimate of the minimum amount of unsaturated fatty acid required for growth of Escherichia coli by Cronan (1973)10.1186/1472-6750-8-61
/ BMC Biotechnol / Plasmid selection in Escherichia coli using an endogenous essential gene marker by Goh (2008)10.1021/bi00294a032
/ Biochemistry / β-Hydroxydecanoyl thioester dehydrase does not catalyze a rate-limiting step in Escherichia coli unsaturated fatty acid synthesis by Clark (1983)10.1074/jbc.M208920200
/ J Biol Chem / A new mechanism for anaerobic unsaturated fatty acid formation in Streptococcus pneumoniae by Marrakchi (2002)10.1128/AAC.46.5.1246-1252.2002
/ Antimicrob Agents Chemother / A missense mutation in the fabB (β-ketoacyl-acyl carrier protein synthase I) gene confers thiolactomycin resistance to Escherichia coli by Jackowski (2002)10.1016/S0021-9258(19)85692-2
/ J Biol Chem / β-Ketoacyl-acyl carrier protein synthase II of Escherichia coli. Evidence for function in the thermal regulation of fatty acid synthesis by Garwin (1980)10.1074/jbc.M403874200
/ J Biol Chem / Functional replacement of the FabA and FabB proteins of Escherichia coli fatty acid synthesis by Enterococcus faecalis FabZ and FabF homologues by Wang (2004)10.1128/JB.154.1.221-230.1983
/ J Bacteriol / Genetic and biochemical analyses of Escherichia coli mutants altered in the temperature-dependent regulation of membrane lipid composition by Ulrich (1983)10.1128/JB.01623-06
/ J Bacteriol / Identification of genes involved in swarming motility using a Pseudomonas aeruginosa PAO1 Mini-Tn5-lux mutant library by Overhage (2007)10.1016/S0014-5793(96)01437-8
/ FEBS Lett / Cloning of the fabF gene in an expression vector and in vitro characterization of recombinant fabF and fabB encoded enzymes from Escherichia coli by Edwards (1997)10.1016/S0021-9258(18)32888-6
/ J Biol Chem / Thermal regulation of membrane fluidity in Escherichia coli. Effects of overproduction of β-ketoacyl-acyl carrier protein synthase I by de Mendoza (1983){'key': '10.1016/j.plipres.2013.02.002_b0405', 'first-page': '4596', 'article-title': 'Overproduction of a functional fatty acid biosynthetic enzyme blocks fatty acid synthesis in Escherichia coli', 'volume': '180', 'author': 'Subrahmanyam', 'year': '1998', 'journal-title': 'J Biol Chem'}
/ J Biol Chem / Overproduction of a functional fatty acid biosynthetic enzyme blocks fatty acid synthesis in Escherichia coli by Subrahmanyam (1998)10.1194/jlr.R800005-JLR200
/ J Lipid Res / Acyltransferases in bacterial glycerophospholipid synthesis by Zhang (2008)10.1016/S0021-9258(19)41128-9
/ J Biol Chem / Regulation of membrane lipid synthesis in Escherichia coli. Accumulation of free fatty acids of abnormal length during inhibition of phospholipid synthesis by Cronan (1975)10.1146/annurev.biochem.74.082803.133524
/ Annu Rev Biochem / The structural biology of type II fatty acid biosynthesis by White (2005)10.1016/S0969-2126(96)00030-5
/ Structure / Structure of a dehydratase-isomerase from the bacterial pathway for biosynthesis of unsaturated fatty acids: two catalytic activities in one active site by Leesong (1996)10.1128/JB.01275-07
/ J Bacteriol / Isolation and characterization of unsaturated fatty acid auxotrophs of Streptococcus pneumoniae and Streptococcus mutans by Altabe (2007)10.1128/JB.186.13.4152-4158.2004
/ J Bacteriol / The fabM gene product of Streptococcus mutans is responsible for the synthesis of monounsaturated fatty acids and is necessary for survival at low pH by Fozo (2004)10.1074/jbc.M504637200
/ J Biol Chem / Domain swapping between Enterococcus faecalis FabN and FabZ proteins localizes the structural determinants for isomerase activity by Lu (2005)10.1111/j.1365-2958.2011.07826.x
/ Mol Microbiol / Identification of a conserved protein involved in anaerobic unsaturated fatty acid synthesis in Neiserria gonorrhoeae: implications for facultative and obligate anaerobes that lack FabA by Isabella (2011)10.1186/1471-2180-9-119
/ BMC Microbiol / Functions of the Clostridium acetobutylicium FabF and FabZ proteins in unsaturated fatty acid biosynthesis by Zhu (2009)10.1128/JB.185.10.3228-3231.2003
/ J Bacteriol / The Bacillus subtilis acyl lipid desaturase is a D5 desaturase by Altabe (2003)10.1111/j.1365-2958.2001.02322.x
/ Mol Microbiol / Role of the Bacillus subtilis fatty acid desaturase in membrane adaptation during cold shock by Weber (2001)10.1128/JB.180.8.2194-2200.1998
/ J Bacteriol / A Bacillus subtilis gene induced by cold shock encodes a membrane phospholipid desaturase by Aguilar (1998)10.1111/j.1365-2958.2006.05088.x
/ Mol Microbiol / Two aerobic pathways for the formation of unsaturated fatty acids in Pseudomonas aeruginosa by Zhu (2006)10.1073/pnas.0510144103
/ Proc Natl Acad Sci USA / Structure and mechanism of the Propionibacterium acnes polyunsaturated fatty acid isomerase by Liavonchanka (2006)10.1001/archderm.1970.04000010038005
/ Arch Dermatol / Corynebacterium acnes from human skin. Identification by morphologic, cultural, biochemical, serological, and chromatographic methods by Ray (1970)10.1128/JB.94.5.1300-1305.1967
/ J Bacteriol / Cultural characteristics and fatty acid composition of Corynebacterium acnes by Moss (1967)10.1016/j.bbalip.2012.08.018
/ Biochim Biophys Acta / Phosphatidic acid synthesis in bacteria by Yao (2013)10.1128/jb.176.10.2814-2821.1994
/ J Bacteriol / Inhibition of fatty acid synthesis in Escherichia coli in the absence of phospholipid synthesis and release of inhibition by thioesterase action by Jiang (1994)10.1128/JB.109.2.668-677.1972
/ J Bacteriol / Effect of glycerol deprivation on the phospholipid metabolism of a glycerol auxotroph of Staphylococcus aureus by Ray (1972)10.1128/JB.112.1.413-420.1972
/ J Bacteriol / Consequences of glycerol deprivation on the synthesis of membrane components in a glycerol auxotroph of Staphylococcus aureus by Ray (1972)10.1016/S0021-9258(19)40921-6
/ J Biol Chem / Mutants of Escherichia coli defective in membrane phospholipid synthesis: properties of wild type and Km defective sn-glycerol-3-phosphate acyltransfersae activities by Bell (1975)10.1016/j.molcel.2006.06.030
/ Mol Cell / Acyl-phosphates initiate membrane phospholipid synthesis in Gram-positive pathogens by Lu (2006)10.1016/S0021-9258(17)44076-2
/ J Biol Chem / Altered acyltransferase activity in Escherichia coli associated with mutations in acyl coenzyme A synthetase by Greenway (1983)10.1016/S0021-9258(19)63377-6
/ J Biol Chem / Mechanism of the apparent regulation of Escherichia coli unsaturated fatty acid synthesis by exogenous oleic acid by Polacco (1977)10.1128/JB.144.1.462-464.1980
/ J Bacteriol / The positional distribution of fatty acids in Escherichia coli phospholipids is not regulated by sn-glycerol 3-phosphate levels by Goelz (1980)10.1016/S0021-9258(19)70037-4
/ J Biol Chem / Phospholipid synthesis in Escherichia coli. Characteristics of fatty acid transfer from acyl-acyl carrier protein to sn-glycerol-3-phosphate by Rock (1981)10.1016/0005-2736(78)90157-8
/ Biochim Biophys Acta / An estimate of the minimum amount of fluid lipid required for the growth of Escherichia coli by Jackson (1978)10.1128/JB.120.1.227-233.1974
/ J Bacteriol / Mutants of Escherichia coli defective in membrane phospholipid synthesis: mapping of sn-glycerol 3-phosphate acyltransferase Km mutants by Cronan (1974)10.1128/JB.181.6.1944-1946.1999
/ J Bacteriol / A missense mutation accounts for the defect in the glycerol-3-phosphate acyltransferase expressed in the plsB26 mutant by Heath (1999)10.1128/JB.160.2.711-717.1984
/ J Bacteriol / Sn-Glycerol-3-phosphate auxotrophy of plsB strains of Escherichia coli: evidence that a second mutation, plsX, is required by Larson (1984)10.1128/JB.00602-07
/ J Bacteriol / Coupling of fatty acid and phospholipid synthesis in Bacillus subtilis by Paoletti (2007)10.1074/jbc.M700374200
/ J Biol Chem / Topology and active site of PlsY: the bacterial acylphosphate: glycerol-3-phosphate acyltransferase by Lu (2007)10.1186/1471-2180-7-69
/ BMC Microbiol / Involvement of the YneS/YgiH and PlsX proteins in phospholipid biosynthesis in both Bacillus subtilis and Escherichia coli by Yoshimura (2007)10.1266/ggs.83.433
/ Genes Genet Syst / Involvement of PlsX and the acyl-phosphate dependent sn-glycerol-3-phosphate acyltransferase PlsY in the initial stage of glycerolipid synthesis in Bacillus subtilis by Hara (2008)10.1016/S0021-9258(17)40257-2
/ J Biol Chem / Relation of turnover of membrane phospholipids to synthesis of membrane-derived oligosaccharides of Escherichia coli by Schulman (1977)10.1128/JB.137.2.860-868.1979
/ J Bacteriol / Diglyceride kinase mutants of Escherichia coli: inner membrane association of 1,2-diglyceride and its relation to synthesis of membrane-derived oligosaccharides by Raetz (1979)10.1073/pnas.78.9.5513
/ Proc Natl Acad Sci USA / Biosynthesis of membrane-derived oligosaccharides: a periplasmic phosphoglyceroltransferase by Goldberg (1981)10.1016/S0021-9258(17)34773-7
/ J Biol Chem / Neutral lipid accumulation in the membranes of Escherichia coli mutants lacking diglyceride kinase by Raetz (1978)10.1126/science.3941890
/ Science / Osmotic adaptation by Gram-negative bacteria: possible role for periplasmic oligosaccharides by Miller (1986)10.1073/pnas.79.4.1092
/ Proc Natl Acad Sci USA / Osmotic regulation and biosynthesis of membrane-derived oligosaccharides in Escherichia coli by Kennedy (1982)10.1128/JB.160.3.976-981.1984
/ J Bacteriol / Biosynthesis of membrane-derived oligosaccharides: characterization of mdoB mutants defective in phosphoglycerol transferase I activity by Jackson (1984)10.1016/S0378-1097(03)00323-9
/ FEMS Microbiol Lett / Membrane-derived oligosaccharides (MDOs) are essential for sodium dodecyl sulfate resistance in Escherichia coli by Rajagopal (2003)10.1016/S0301-4622(99)00005-8
/ Biophys Chem / Effects of diacylglycerol on the structure and phase behaviour of non-bilayer forming phospholipid by Takahashi (1999)10.1074/jbc.M801812200
/ J Biol Chem / Diacylglycerol specifically blocks spontaneous integration of membrane proteins and allows detection of a factor-assisted integration by Kawashima (2008)10.1146/annurev-biophys-050511-102330
/ Annu Rev Biophys / Prokaryotic diacylglycerol kinase and undecaprenol kinase by Van Horn (2011)10.1126/science.1171716
/ Science / Solution nuclear magnetic resonance structure of membrane-integral diacylglycerol kinase by Van Horn (2009)10.1111/j.1365-2958.2011.07641.x
/ Mol Microbiol / Antagonistic regulation of dgkA and plsB genes of phospholipid synthesis by multiple stress responses in Escherichia coli by Wahl (2011)10.1074/jbc.M703536200
/ J Biol Chem / Identification of a soluble diacylglycerol kinase required for lipoteichoic acid production in Bacillus subtilis by Jerga (2007)10.1073/pnas.0701821104
/ Proc Natl Acad Sci USA / Synthesis of glycerol phosphate lipoteichoic acid in Staphylococcus aureus by Grundling (2007)10.1128/JB.01221-08
/ J Bacteriol / Pleiotropic roles of polyglycerolphosphate synthase of lipoteichoic acid in growth of Staphylococcus aureus cells by Oku (2009)10.1128/IAI.13.5.1408-1417.1976
/ Infect Immun / Effects of a streptococcal lipoteichoic acid on host responses in mice by Miller (1976)10.1128/jb.179.9.2879-2883.1997
/ J Bacteriol / Effect of lipoteichoic acid on thermotropic membrane properties by Gutberlet (1997)10.1128/jb.178.6.1565-1571.1996
/ J Bacteriol / An autolysin ring associated with cell separation of Staphylococcus aureus by Yamada (1996)10.1128/IAI.01140-07
/ Infect Immun / Lipoteichoic acid is important in innate immune responses to Gram-positive bacteria by Seo (2008)10.1128/JB.01683-06
/ J Bacteriol / Genes required for glycolipid synthesis and lipoteichoic acid anchoring in Staphylococcus aureus by Grundling (2007)10.1074/jbc.M805962200
/ J Biol Chem / Molecular determinants for interfacial binding and conformational change in a soluble diacylglycerol kinase by Jerga (2009)10.1016/j.str.2008.03.019
/ Structure / Analysis of the Staphylococcus aureus DgkB structure reveals a common catalytic mechanism for the soluble diacylglycerol kinases by Miller (2008)10.1074/jbc.M504929200
/ J Biol Chem / Phospholipids as determinants of membrane protein topology. Phosphatidylethanolamine is required for the proper topological organization of the g-aminobutyric acid permease (GabP) of Escherichia coli by Zhang (2005)10.1074/jbc.M602565200
/ J Biol Chem / Phosphatidylethanolamine and monoglucosyldiacylglycerol are interchangeable in supporting topogenesis and function of the polytopic membrane protein lactose permease by Xie (2006)10.1016/S0021-9258(18)91247-0
/ J Biol Chem / Metabolism and function of bacterial lipids II. Biosynthesis of phospholipids in Escherichia coli by Kanfer (1964)10.1016/S0021-9258(18)41520-7
/ J Biol Chem / Rab3A GTPase-activating protein-inhibiting activity of Rabphilin-3A, a putative Rab3A target protein by Kishida (1993)10.1016/S0021-9258(17)38989-5
/ J Biol Chem / Purfication and properties of the membrane-bound CDP-diglyceride synthetase from Escherichia coli by Sparrow (1985)10.1016/S0021-9258(19)86078-7
/ J Biol Chem / Phosphatidic acid accumulation in the membranes of Escherichia coli mutants defective in CDP-diglyceride synthetase by Ganong (1980)10.1016/S0021-9258(19)68376-6
/ J Biol Chem / Massive accumulation of phosphatidic acid in conditionally lethal CDP-diglyceride synthetase mutants and cytidine auxotrophs of Escherichia coli by Ganong (1982)10.1128/JB.153.2.731-738.1983
/ J Bacteriol / PH-sensitive CDP-diglyceride synthetase mutants of Escherichia coli: phenotypic suppression by mutations at a second site by Ganong (1983)10.1073/pnas.82.22.7530
/ Proc Natl Acad Sci USA / Genetic manipulation of membrane phospholipid composition in Escherichia coli: pgsA mutants defective in phosphatidylglycerol synthesis by Miyazaki (1985)10.1074/jbc.M110.199265
/ J Biol Chem / Three phosphatidylglycerol-phosphate phosphatases in the inner membrane of Escherichia coli by Lu (2011)10.1128/jb.177.10.2926-2928.1995
/ J Bacteriol / Phosphatidylinositol cannot substitute for phosphatidylglycerol in supporting cell growth of Escherichia coli by Xia (1995)10.1128/JB.182.2.371-376.2000
/ J Bacteriol / Viability of an Escherichia coli pgsA null mutant lacking detectable phosphatidylglycerol and cardiolipin by Kikuchi (2000)10.1128/JB.181.12.3666-3673.1999
/ J Bacteriol / Role in cell permeability of an essential two-component system in Staphylococcus aureus by Martin (1999)10.1266/ggs.84.191
/ Genes Genet Syst / Induction of extracytoplasmic function sigma factors in Bacillus subtilis cells with membranes of reduced phosphatidylglycerol content by Hashimoto (2009)10.1128/JB.99.1.298-303.1969
/ J Bacteriol / Phospholipid composition of Bacillus subtilis by Den Kamp (1969)10.1128/JB.108.1.219-226.1971
/ J Bacteriol / Metabolism of phosphatidylglycerol, lysylphosphatidylglycerol, and cardiolipin of Staphylococcus aureus by Short (1971)10.1128/JB.184.19.5418-5425.2002
/ J Bacteriol / Envelope disorder of Escherichia coli cells lacking phosphatidylglycerol by Suzuki (2002)10.1128/jb.170.2.775-780.1988
/ J Bacteriol / Disruption of the Escherichia coli cls gene responsible for cardiolipin synthesis by Nishijima (1988)10.1016/S0021-9258(17)34655-0
/ J Biol Chem / Function of phospholipids in Escherichia coli. Characterization of a mutant deficient in cardiolipin synthesis by Pluschke (1978)10.1016/S1388-1981(99)00193-6
/ Biochim Biophys Acta / A second Escherichia coli protein with CL synthase activity by Guo (2000)10.1073/pnas.1212797109
/ Proc Natl Acad Sci USA / Discovery of a cardiolipin synthase utilizing phosphatidylethanolamine and phosphatidylglycerol as substrates by Tan (2012)10.1186/1471-2180-11-13
/ BMC Microbiol / Staphylococcus aureus requires cardiolipin for survival under conditions of high salinity by Tsai (2011)10.1016/S0021-9258(19)67791-4
/ J Biol Chem / Sequence and inactivation of the pss gene of Escherichia coli. Phosphatidylethanolamine may not be essential for cell viability by DeChavigny (1991)10.1016/0076-6879(92)09036-3
/ Methods Enzymol / Phosphatidylserine synthase from Escherichia coli by Dowhan (1992)10.1021/bi00669a003
/ Biochemistry / Ribosomal-associated phosphatidylserine synthetase from Escherichia coli: purification by substrate-specific elution from phosphocellulose using cytidine 5′-diphospho-1,2-diacyl-sn-glycerol by Larson (1976)10.1128/jb.165.3.805-812.1986
/ J Bacteriol / Substrate-induced membrane association of phosphatidylserine synthase from Escherichia coli by Louie (1986)10.1128/JB.95.3.833-843.1968
/ J Bacteriol / Lipids of Salmonella typhimurium and Escherichia coli: structure and metabolism by Ames (1968)10.1016/S0021-9258(19)39709-1
/ J Biol Chem / Studies on the mechanism of formation of the pyruvate prosthetic group of phosphatidylserine decarboxylase from Escherichia coli by Li (1990)10.1016/S0021-9258(17)34384-3
/ J Biol Chem / Phospholipid composition and membrane function in phosphatidylserine decarboxylase mutants of Escherichia coli by Hawrot (1978)10.1016/0014-5793(75)80681-8
/ FEBS Lett / Accumulation of phosphatidylserine in strictly anaerobic lactate fermenting bacteria by van Golde (1975)10.1016/S0163-7827(02)00050-4
/ Prog Lipid Res / Biosynthesis of phosphatidylcholine in bacteria by Sohlenkamp (2003)10.1016/j.bbalip.2012.08.009
/ Biochim Biophys Acta / Phosphatidylcholine biosynthesis and function in bacteria by Geiger (2013)10.1016/S0021-9258(18)97107-3
/ J Biol Chem / Phosphatidylcholine synthesis in Agrobacterium tumefaciens. II. Uptake and utilization of choline by Sherr (1965)10.1099/ijs.0.036087-0
/ Int J Syst Evol Microbiol / Rhodococcus canchipurensis sp. nov., a novel actinomycete isolated from a limestone deposit site in Manipur, India by Nimaichand (2013)10.1074/jbc.M004658200
/ J Biol Chem / Phosphatidylinositol is an essential phospholipid of mycobacteria by Jackson (2000)10.1016/j.bbagen.2011.03.017
/ Biochim Biophys Acta / Inositol lipid metabolism in mycobacteria: biosynthesis and regulatory mechanisms by Morita (2011)10.1007/s10482-012-9757-4
/ Antonie Van Leeuwenhoek / Kineococcus endophytica sp. nov., a novel endophytic actinomycete isolated from a coastal halophyte in Jiangsu, China by Bian (2012)10.1128/jb.173.6.2053-2060.1991
/ J Bacteriol / Phosphatidylinositol, a phospholipid of ice-nucleating bacteria by Kozloff (1991)10.1128/JB.183.11.3506-3514.2001
/ J Bacteriol / Biosynthesis of the glycolipid anchor in lipoteichoic acid of Staphylococcus aureus RN4220: role of YpfP, the diglucosyldiacylglycerol synthase by Kiriukhin (2001)10.1038/35082000
/ Nature / Three-dimensional structure of cyanobacterial photosystem I at 2.5 A resolution by Jordan (2001)10.1046/j.1365-2958.1998.00930.x
/ Mol Microbiol / A UDP glucosyltransferase from Bacillus subtilis successively transfers up to four glucose residues to 1,2-diacylglycerol: expression of ypfP in Escherichia coli and structural analysis of its reaction products by Jorasch (1998)10.1111/j.1432-1033.1984.tb07923.x
/ Eur J Biochem / The role of lipoteichoic acid biosynthesis in membrane lipid metabolism of growing Staphylococcus aureus by Koch (1984)10.1111/j.1574-6968.2011.02260.x
/ FEMS Microbiol Lett / Location, synthesis and function of glycolipids and polyglycerolphosphate lipoteichoic acid in Gram-positive bacteria of the phylum Firmicutes by Reichmann (2011)10.1021/bi00507a010
/ Biochemistry / Reversed cubic phase with membrane glucolipids from Acholeplasma laidlawii. 1H, 2H, and diffusion nuclear magnetic resonance measurements by Wieslander (1981)10.1111/j.1432-1033.1978.tb12212.x
/ Eur J Biochem / Membrane lipid metabolism in Acholeplasma laidlawii A EF 22. Influence of cholesterol and temperature shift-down on incorporation of fatty acids and synthesis of membrane lipid species by Christiansson (1978)10.1016/0005-2736(77)90229-2
/ Biochim Biophys Acta / Qualitative and quantitative variations of membrane lipid species in Acholeplasma laidlawii A by Wieslander (1977)10.1016/0005-2736(95)00132-M
/ Biochim Biophys Acta / Influence of monoglucosyldiacylglycerol and monoacylmonoglucosyldiacylglycerol on the lipid bilayer of the membrane from Acholeplasma laidlawii strain A-EF22 by Niemi (1995)10.1074/jbc.271.12.6801
/ J Biol Chem / Wild-type Escherichia coli cells regulate the membrane lipid composition in a “window” between gel and non-lamellar structures by Morein (1996)10.1021/bi700042x
/ Biochemistry / High cationic charge and bilayer interface-binding helices in a regulatory lipid glycosyltransferase by Lind (2007)10.1111/j.1365-2958.2007.05854.x
/ Mol Microbiol / A Staphylococcus aureus ypfP mutant with strongly reduced lipoteichoic acid (LTA) content: LTA governs bacterial surface properties and autolysin activity by Fedtke (2007)10.1371/journal.ppat.1002217
/ PLoS Pathog / C-di-AMP is a new second messenger in Staphylococcus aureus with a role in controlling cell size and envelope stress by Corrigan (2011)10.1128/MMBR.34.4.365-377.1970
/ Bacteriol Rev / Bacterial glycolipids by Shaw (1970)10.1093/pcp/pcm134
/ Plant Cell Physiol / Digalactosyldiacylglycerol is required for better photosynthetic growth of Synechocystis sp. PCC6803 under phosphate limitation by Awai (2007)10.1093/glycob/7.7.935
/ Glycobiology / Digalactosyl diacylglycerols, plant glycolipids rarely found in bacteria, are major membrane components of bacteroid forms of Bradyrhizobium japonicum by Tang (1997)10.1111/j.1365-2958.2011.07792.x
/ Mol Microbiol / The Mycobacterium tuberculosis Ag85A is a novel diacylglycerol acyltransferase involved in lipid body formation by Elamin (2011)10.1128/JB.186.15.5017-5030.2004
/ J Bacteriol / Induction of a novel class of diacylglycerol acyltransferases and triacylglycerol accumulation in Mycobacterium tuberculosis as it goes into a dormancy-like state in culture by Daniel (2004)10.1007/s00203-001-0355-5
/ Arch Microbiol / Preparative isolation of lipid inclusions from Rhodococcus opacus and Rhodococcus ruber and identification of granule-associated proteins by Kalscheuer (2001)10.1128/MMBR.63.1.21-53.1999
/ Microbiol Mol Biol Rev / Metabolic engineering of poly(3-hydroxyalkanoates): from DNA to plastic by Madison (1999)10.1016/j.plipres.2009.08.002
/ Prog Lipid Res / Amino acid-containing membrane lipids in bacteria by Geiger (2010)10.1111/j.1574-6968.2012.02623.x
/ FEMS Microbiol Lett / Ornithine lipids and their structural modifications: from A to E and beyond by Vences-Guzman (2012)10.1073/pnas.0912930107
/ Proc Natl Acad Sci USA / Sinorhizobium meliloti phospholipase C required for lipid remodeling during phosphorus limitation by Zavaleta-Pastor (2010)10.1046/j.1365-2958.1999.01325.x
/ Mol Microbiol / The regulator gene phoB mediates phosphate stress-controlled synthesis of the membrane lipid diacylglyceryl-N, N,N-trimethylhomoserine in Rhizobium (Sinorhizobium) meliloti by Geiger (1999)10.1016/j.abb.2005.07.001
/ Arch Biochem Biophys / Two enzymes, BtaA and BtaB, are sufficient for betaine lipid biosynthesis in bacteria by Riekhof (2005)10.1073/pnas.1001501107
/ Proc Natl Acad Sci USA / Membrane sphingolipids as essential molecular signals for Bacteroides survival in the intestine by An (2011)10.1016/S0022-2275(20)43045-7
/ J Lipid Res / Identification of ceramide phosphorylethanolamine and ceramide phosphorylglycerol in the lipids of an anaerobic bacterium by LaBach (1969)10.1006/anae.2001.0376
/ Anaerobe / Sphingolipids in bacteria and fungi by Olsen (2012)10.1194/jlr.M400278-JLR200
/ J Lipid Res / Structures and biological activity of phosphorylated dihydroceramides of Porphyromonas gingivalis by Nichols (2004)10.1093/oxfordjournals.jbchem.a132528
/ J Biochem / Occurrence of free ceramides in Bacteroides fragilis NCTC 9343 by Miyagawa (1979)10.1038/nature03407
/ Nature (London) / Recognition of bacterial glycosphingolipids by natural killer T cells by Kinjo (2005)10.1038/nature03408
/ Nature (London) / Exogenous and endogenous glycolipid antigens activate NKT cells during microbial infections by Mattner (2005)10.1016/S0022-5347(17)55344-6
/ J Urol / Anaerobic urinary infections: Bacteroides fragilis bacteremia from the urinary tract by Bagley (1980)10.1074/jbc.270.26.15531
/ J Biol Chem / Regulation of malonyl-CoA metabolism by acyl-acyl carrier protein and β-ketoacyl-acyl carrier protein synthases in Escherichia coli by Heath (1995)10.1128/jb.175.12.3723-3729.1993
/ J Bacteriol / Thiolactomycin resistance in Escherichia coli is associated with the multidrug resistance efflux pump encoded by emrAB by Furukawa (1993)10.1021/bi0520479
/ Biochemistry / The structure of the carboxyltransferase component of acetyl-coA carboxylase reveals a zinc-binding motif unique to the bacterial enzyme by Bilder (2006)10.1073/pnas.1204604109
/ Proc Natl Acad Sci USA / Feedback regulation of plastidic acetyl-CoA carboxylase by 18:1-acyl carrier protein in Brassica napus by Andre (2012)10.1016/S0021-9258(19)41128-9
/ J Biol Chem / Regulation of membrane lipid synthesis in Escherichia coli. Accumulation of free fatty acids of abnormal length during inhibition of phospholipid synthesis by Cronan (1975)10.1093/emboj/17.5.1183
/ EMBO J / Crystal structure of β-ketoacyl-acyl carrier protein synthase II from E. coli reveals the molecular architecture of condensing enzymes by Huang (1998)10.1074/jbc.274.10.6031
/ J Biol Chem / Structure of the complex between the antibiotic cerulenin and its target, β-ketoacyl-acyl carrier protein synthase by Moche (1999)10.1074/jbc.M007101200
/ J Biol Chem / Inhibition of β-ketoacyl-[acyl carrier protein] synthases by thiolactomycin and cerulenin: structure and mechanism by Price (2001)10.1016/S0969-2126(01)00583-4
/ Structure / Structures of β-ketoacyl-acyl carrier protein synthase I complexed with fatty acids elucidate its catalytic machinery by Olsen (2001)10.1074/jbc.271.44.27795
/ J Biol Chem / Regulation of fatty acid elongation and initiation by acyl-acyl carrier protein in Escherichia coli by Heath (1996)10.1073/pnas.70.2.385
/ Proc Natl Acad Sci USA / Regulation of macromolecular biosynthesis in a mutant of Escherichia coli defective in membrane phospholipid biosynthesis by Glaser (1973)10.1128/JB.123.1.128-136.1975
/ J Bacteriol / Role of adenylate kinase in the regulation of macromolecular biosynthesis in a putative mutant of Escherichia coli defective in membrane phospholipid biosynthesis by Glaser (1975)10.1128/JB.117.3.1065-1076.1974
/ J Bacteriol / Mutants of Escherichia coli defective in membrane phospholipid synthesis: macromolecular synthesis in an sn-glycerol 3-phosphate acyltransferase Km mutant by Bell (1974)10.1016/S0021-9258(19)40692-3
/ J Biol Chem / Mutants of Escherichia coli defective in membrane phospholipid synthesis. Effect of cessation of net phospholipid synthesis on cytoplasmic and outer membranes by McIntyre (1975)10.1016/S0021-9258(17)40187-6
/ J Biol Chem / Mutants of Escherichia coli defective in membrane phospholipid synthesis. Effects of cessation and reinitiation of phospholipid synthesis on macromolecular synthesis and phospholipid turnover by McIntyre (1977)10.1128/AAC.3.5.549
/ Antimicrob Agents Chemother / Inhibition of lipid synthesis in Escherichia coli cells by the antibiotic cerulenin by Goldberg (1973)10.1007/BF02425329
/ Mol Gen Genet / Interaction of alleles of the relA, relC and spoT genes in Escherichia coli: analysis of the interconversion of GTP, ppGpp and pppGpp by Fiil (1977)10.1016/j.mib.2008.02.001
/ Curr Opin Microbiol / Control of bacterial transcription, translation and replication by (p)ppGpp by Srivatsan (2008)10.1016/S0021-9258(19)43280-8
/ J Biol Chem / Stringent control of fatty acid synthesis in Escherichia coli. Possible regulation of acetyl coenzyme A carboxylase by ppGpp by Polakis (1973)10.1016/S0021-9258(19)40775-8
/ J Biol Chem / Acylation of sn-glycerol-3-phosphate in Escherichia coli, Study of reaction with native palmitoyl-acyl carrier protein by Ray (1975)10.1016/S0021-9258(19)41255-6
/ J Biol Chem / The involvement of guanosine 5′-diphosphate-3′-diphosphate in the regulation of phospholipid biosynthesis in Escherichia coli. Lack of ppGpp inhibition of acyltransfer from acyl-ACP to sn-glycerol-3-phosphate by Lueking (1975)10.1146/annurev.micro.62.081307.162903
/ Annu Rev Microbiol / (p)ppGpp still magical? by Potrykus (2008)10.1016/S0021-9258(19)69763-2
/ J Biol Chem / Cloning of genes involved in membrane lipid synthesis. Effects of amplification of phosphatidylserine synthase in Escherichia coli by Ohta (1981)10.1016/S0021-9258(18)67041-3
/ J Biol Chem / Regulation of the balanced synthesis of membrane phospholipids. Experimental test of models for regulation in Escherichia coli by Jackson (1986)10.1128/JB.147.2.552-562.1981
/ J Bacteriol / Cloning of genes involved in membrane lipid synthesis: effects of amplification of phosphatidylglycerophosphate synthase in Escherichia coli by Ohta (1981)10.1073/pnas.83.19.7236
/ Proc Natl Acad Sci USA / An essential function for acyl carrier protein in the biosynthesis of membrane-derived oligosaccharides of Escherichia coli by Therisod (1986)10.1271/bbb.60.111
/ Biosci Biotechnol Biochem / A regulatory mechanism for the balanced synthesis of membrane phospholipid species in Escherichia coli by Saha (1996)10.1016/S0021-9258(17)38234-0
/ J Biol Chem / Identification of bound pyruvate essential for the activity of phosphatidylserine decarboxylase of Escherichia coli by Satre (1976)10.1016/S0021-9258(18)37988-2
/ J Biol Chem / Structural characterization of the Escherichia coli phosphatidylserine decarboxylase by Li (1988)10.1146/annurev.bi.53.070184.002041
/ Annu Rev Biochem / Pyruvoyl enzymes by Recsei (1984)10.1371/journal.ppat.1000556
/ PLoS Pathog / Vibrio cholerae proteome-wide screen for immunostimulatory proteins identifies phosphatidylserine decarboxylase as a novel Toll-like receptor 4 agonist by Thanawastien (2009)10.1128/JB.180.1.100-106.1998
/ J Bacteriol / Cloning, sequencing, and disruption of the Bacillus subtilis psd gene coding for phosphatidylserine decarboxylase by Matsumoto (1998)10.1016/S0076-6879(97)80104-8
/ Methods Enzymol / Phosphatidylserine decarboxylases: pyruvoyl-dependent enzymes from bacteria to mammals by Dowhan (1997)10.1111/j.1365-2958.2011.07576.x
/ Mol Microbiol / Broad-spectrum antimicrobial peptide resistance by MprF-mediated aminoacylation and flipping of phospholipids by Ernst (2011)10.1074/jbc.M111.226886
/ J Biol Chem / Multiple peptide resistance factor (MprF)-mediated resistance of Staphylococcus aureus against antimicrobial peptides coincides with a modulated peptide interaction with artificial membranes comprising lysyl-phosphatidylglycerol by Andra (2011)10.1371/journal.ppat.1000660
/ PLoS Pathog / The bacterial defensin resistance protein MprF consists of separable domains for lipid lysinylation and antimicrobial peptide repulsion by Ernst (2009)10.1128/AAC.00429-10
/ Antimicrob Agents Chemother / Regulation of mprF by antisense RNA restores daptomycin susceptibility to daptomycin-resistant isolates of Staphylococcus aureus by Rubio (2011)10.1084/jem.193.9.1067
/ J Exp Med / Staphylococcus aureus resistance to human defensins and evasion of neutrophil killing via the novel virulence factor MprF is based on modification of membrane lipids with l-lysine by Peschel (2001)10.1099/00221287-148-11-3331
/ Microbiology / MprF-mediated lysinylation of phospholipids in Bacillus subtilis–protection against bacteriocins in terrestrial habitats? by Staubitz (2002)10.1111/j.1365-2958.2008.06562.x
/ Mol Microbiol / Adaptation of Pseudomonas aeruginosa to various conditions includes tRNA-dependent formation of alanyl-phosphatidylglycerol by Klein (2009)10.1074/jbc.M109.046367
/ J Biol Chem / Broad range amino acid specificity of RNA-dependent lipid remodeling by multiple peptide resistance factors by Roy (2009)10.1073/pnas.0702159104
/ Proc Natl Acad Sci USA / Gram-positive three-component antimicrobial peptide-sensing system by Li (2007)10.1128/AAC.00432-10
/ Antimicrob Agents Chemother / VraSR two-component regulatory system contributes to mprF-mediated decreased susceptibility to daptomycin in in vivo-selected clinical strains of methicillin-resistant Staphylococcus aureus by Mehta (2012)10.1159/000219377
/ Contrib Microbiol / Bacterial sensing of antimicrobial peptides by Otto (2009)10.1111/j.1365-2958.2007.05986.x
/ Mol Microbiol / The antimicrobial peptide-sensing system aps of Staphylococcus aureus by Li (2007)10.1128/jb.178.6.1699-1706.1996
/ J Bacteriol / The Pseudomonas putida peptidoglycan-associated outer membrane lipoprotein is involved in maintenance of the integrity of the cell cell envelope by Rodriguez-Herva (1996)10.1128/IAI.00682-10
/ Infect Immun / Lipoproteins of bacterial pathogens by Kovacs-Simon (2011)10.1128/JB.188.8.2761-2773.2006
/ J Bacteriol / A database of bacterial lipoproteins (DOLOP) with functional assignments to predicted lipoproteins by Babu (2006)10.1016/S0021-9258(20)82124-3
/ J Biol Chem / Turnover of fatty acids in the 1-position of phosphatidylethanolamine in Escherichia coli by Rock (1984)10.1016/S0021-9258(18)67387-9
/ J Biol Chem / Transfer of fatty acids from the 1-position of phosphatidylethanolamine to the major outer membrane lipoprotein of Escherichia coli by Jackowski (1986)10.1016/S0021-9258(18)92916-9
/ J Biol Chem / Phosphatidylethanolamine is not essential for the N-acylation of apolipoprotein in Escherichia coli by Gupta (1991)10.1016/S0021-9258(17)42029-1
/ J Biol Chem / Sequence and function of the aas gene in Escherichia coli by Jackowski (1994)10.1016/S0021-9258(18)83245-8
/ J Biol Chem / 2-Acylglycerolphosphoethanolamine acyltransferase/acyl-acyl carrier protein synthetase is a membrane-associated acyl carrier protein binding protein by Cooper (1989)10.1016/0076-6879(92)09015-U
/ Methods Enzymol / 2-Acylglycerophosphoethanolamine acyltransferase/acyl-[acyl-carrier-protein] synthetase from Escherichia coli by Jackowski (1992)10.1016/S0021-9258(18)92769-9
/ J Biol Chem / Isolation and characterization of Escherichia coli K-12 mutants lacking both 2-acyl-glycerophosphoethanolamine acyltransferase and acyl-acyl carrier protein synthetase activity by Hsu (1991)10.1021/bi060842w
/ Biochemistry / The soluble acyl-acyl carrier protein synthetase of Vibrio harveyi B392 is a member of the medium chain acyl-CoA synthetase family by Jiang (2006)10.1093/oxfordjournals.jbchem.a133791
/ J Biochem (Tokyo) / Transacylation between diacylphospholipids and 2-acyl lysophospholipids catalyzed by Escherichia coli extract by Homma (1982)10.1016/S0021-9258(19)41297-0
/ J Biol Chem / Lysophospholipase of Escherichia coli by Doi (1975)10.1016/S0021-9258(18)61170-6
/ J Biol Chem / Biosynthesis of lipid A precursors in Escherichia coli. A membrane-bound enzyme that transfers a palmitoyl residue from a glycerophospholipid to lipid X by Brozek (1987)10.1093/emboj/19.19.5071
/ EMBO J / Transfer of palmitate from phospholipids to lipid A in outer membranes of Gram-negative bacteria by Bishop (2000)10.1074/jbc.M414368200
/ J Biol Chem / Lysophospholipid flipping across the Escherichia coli inner membrane catalyzed by a transporter (LplT) belonging to the major facilitator superfamily by Harvat (2005)10.1111/j.1742-4658.2010.07990.x
/ FEBS J / Structural evidence of α-aminoacylated lipoproteins of Staphylococcus aureus by Asanuma (2011)10.1074/jbc.M809618200
/ J Biol Chem / The triacylated ATP binding cluster transporter substrate-binding lipoprotein of Staphylococcus aureus functions as a native ligand for Toll-like receptor 2 by Kurokawa (2009)10.1074/jbc.M900429200
/ J Biol Chem / Characterization of N-terminal structure of TLR2-activating lipoprotein in Staphylococcus aureus by Tawaratsumida (2009)10.1128/JB.00314-12
/ J Bacteriol / Environment-mediated accumulation of diacyl lipoproteins over their triacyl counterparts in Staphylococcus aureus by Kurokawa (2012)10.1016/j.bbalip.2004.01.002
/ Biochim Biophys Acta / Uptake and remodeling of exogenous phosphatidylethanolamine in E. coli by Kol (2004)10.1128/JB.05450-11
/ J Bacteriol / FadD is required for utilization of endogenous fatty acids released from membrane lipids by Pech-Canul (2011)10.1194/jlr.R800046-JLR200
/ J Lipid Res / Transcriptional regulation in bacterial membrane lipid synthesis by Zhang (2009)10.1016/S0021-9258(18)42497-0
/ J Biol Chem / Characterization of FadR, a global transcriptional regulator of fatty acid metabolism in Escherichia coli. Interaction with the fadB promoter is prevented by long chain fatty acyl coenzyme A by DiRusso (1992)10.1074/jbc.M109.023440
/ J Biol Chem / Escherichia coli unsaturated fatty acid synthesis: complex transcription of the fabA gene and in vivo identification of the essential reaction catalyzed by FabB by Feng (2009)10.1128/JB.00516-10
/ J Bacteriol / Overlapping repressor binding sites result in additive regulation of Escherichia coli FadH by FadR and ArcA by Feng (2010)10.1046/j.1365-2958.1998.00645.x
/ Mol Microbiol / The fats of Escherichia coli during infancy and old age: regulation by global regulators, alarmones and lipid intermediates by DiRusso (1998)10.1099/mic.0.28912-0
/ Microbiology / Transcriptional regulation of the fad regulon genes of Escherichia coli by ArcA by Cho (2006)10.1128/JB.117.3.1178-1183.1974
/ J Bacteriol / Fatty acid degradation in Escherichia coli: requirement of cyclic adenosine monophosphate and cyclic adenosine monophosphate receptor protein for enzyme synthesis by Pauli (1974)10.1128/jb.179.5.1819-1823.1997
/ J Bacteriol / In vivo evidence that acyl coenzyme A regulates DNA binding by the Escherichia coli FadR global transcription factor by Cronan (1997)10.1074/jbc.273.50.33652
/ J Biol Chem / Fatty acyl-CoA binding domain of the transcription factor FadR – Characterization by deletion, affinity labeling, and isothermal titration calorimetry by DiRusso (1998)10.1126/science.1097524
/ Science / Crystal structure of the long-chain fatty acid transporter FadL by van den (2004)10.1007/BF00280384
/ Mol Gen Genet / Osmoregulation of the fatty acid receptor gene fadL in Escherichia coli by Higashitani (1993)10.1016/S0021-9258(17)38934-2
/ J Biol Chem / Pathways for the incorporation of exogenous fatty acids into phosphatidylethanolamine in Escherichia coli by Rock (1985)10.1128/JB.00835-09
/ J Bacteriol / A New Member of Escherichia coli fad Regulon: transcriptional regulation of fadM (ybaW) by Feng (2009)10.1021/bi801074e
/ Biochemistry / A novel paradigm of fatty acid β-oxidation exemplified by the thioesterase-dependent partial degradation of conjugated linoleic acid that fully supports growth of Escherichia coli by Nie (2008)10.1021/bi800595f
/ Biochemistry / Identification and characterization of Escherichia coli thioesterase III that functions in fatty acid β-oxidation by Nie (2008)10.1371/journal.pone.0046275
/ PLoS ONE / Crosstalk of Escherichia coli FadR with global regulators in expression of fatty acid transport genes by Feng (2012)10.1128/jb.178.15.4704-4709.1996
/ J Bacteriol / Regulated expression of a repressor protein: FadR activates iclR by Gui (1996)10.1128/JB.183.20.5982-5990.2001
/ J Bacteriol / Escherichia coli FadR positively regulates transcription of the fabB fatty acid biosynthetic gene by Campbell (2001)10.1016/0022-2836(91)90574-P
/ J Mol Biol / Escherichia coli transcription factor that both activates fatty acid synthesis and represses fatty acid degradation by Henry (1991)10.1016/S0021-9258(18)42497-0
/ J Biol Chem / Characterization of FadR, a global transcriptional regulator of fatty acid metabolism in Escherichia coli. Interaction with the fadB promoter is prevented by long chain fatty acyl coenzyme As by DiRusso (1992)10.1093/emboj/20.8.2041
/ EMBO J / The structural basis of acyl coenzyme A-dependent regulation of the transcription factor FadR by van Aalten (2001)10.1093/emboj/19.19.5167
/ EMBO J / Crystal structure of FadR, a fatty acid-responsive transcription factor with a novel acyl coenzyme A-binding fold by van Aalten (2000)10.1107/S0907444900000937
/ Acta Crystallogr D Biol Crystallogr / Crystallization and X-ray diffraction studies of the fatty-acid responsive transcription factor FadR from Escherichia coli by van Aalten (2000)10.1074/jbc.M100195200
/ J Biol Chem / The FadR-DNA complex: transcriptional control of fatty acid metabolism in Escherichia coli by Xu (2001)10.1074/jbc.M504054200
/ J Biol Chem / Unexpected functional diversity among FadR fatty acid transcriptional regulatory proteins by Iram (2005)10.1074/jbc.M606831200
/ J Biol Chem / Organization and function of the YsiA regulon of Bacillus subtilis involved in fatty acid degradation by Matsuoka (2007)10.1111/j.1365-2958.2011.07748.x
/ Mol Microbiol / The Vibrio cholerae fatty acid regulatory protein, FadR, represses transcription of plsB, the gene encoding the first enzyme of membrane phospholipid biosynthesis by Feng (2011)10.1073/pnas.0803281105
/ Proc Natl Acad Sci USA / A defined transposon mutant library and its use in identifying motility genes in Vibrio cholerae by Cameron (2008)10.1038/msb4100050
/ Mol Syst Biol / Construction of Escherichia coli K-12 in-frame, single-gene knockout mutants: the Keio collection by Baba (2006)10.1128/JB.188.2.599-608.2006
/ J Bacteriol / The β-oxidation systems of Escherichia coli and Salmonella enterica are not functionally equivalent by Iram (2006)10.1128/JB.01016-08
/ J Bacteriol / Regulation of fatty acid metabolism by FadR is essential for Vibrio vulnificus to cause infection of mice by Brown (2008)10.1128/JB.00404-09
/ J Bacteriol / DesT coordinates the expression of anaerobic and aerobic pathways for unsaturated fatty acid biosynthesis in Pseudomonas aeruginosa by Subramanian (2010)10.1111/j.1365-2958.2007.05934.x
/ Mol Microbiol / A Pseudomonas aeruginosa transcription factor that senses fatty acid structure by Zhang (2007)10.1038/nsmb.1847
/ Nat Struct Mol Biol / Transcriptional regulation of membrane lipid homeostasis by Miller (2010)10.1074/jbc.M201399200
/ J Biol Chem / The FabR (YijC) transcription factor regulates unsaturated fatty acid biosynthesis in Escherichia coli by Zhang (2002)10.1111/j.1365-2958.2011.07564.x
/ Mol Microbiol / Complex binding of the FabR repressor of bacterial unsaturated fatty acid biosynthesis to its cognate promoters by Feng (2011)10.1074/jbc.M109.068239
/ J Biol Chem / Transcriptional regulation of membrane lipid homeostasis in Escherichia coli by Zhu (2009)10.1093/nar/29.3.774
/ Nucleic Acids Res / Phylogenetic footprinting of transcription factor binding sites in proteobacterial genomes by McCue (2001)10.1128/jb.165.2.434-442.1986
/ J Bacteriol / Opp-lac Operon fusions and transcriptional regulation of the Escherichia coli trp-linked oligopeptide permease by Andrews (1986)10.1021/bi100136n
/ Biochemistry / A novel role of malonyl-ACP in lipid homeostasis by Martinez (2010)10.1038/sj.emboj.7601284
/ EMBO J / Structural basis of lipid biosynthesis regulation in Gram-positive bacteria by Schujman (2006)10.1371/journal.ppat.1003108
/ PLoS Pathog / Structural basis for feed-rorward transcriptional regulation of membrane lipid homeostasis in Staphylococcus aureus by Albanesi (2013)10.1111/j.1365-2958.2008.06202.x
/ Mol Microbiol / A malonyl-CoA-dependent switch in the bacterial response to a dysfunction of lipid metabolism by Schujman (2008)10.1016/S0021-9258(18)33888-2
/ J Biol Chem / Regulation of phospholipid synthesis in Escherichia coli. Composition of the acyl-acyl carrier protein pool in vivo by Rock (1982)10.1016/S0021-9258(17)43791-4
/ J Biol Chem / Ratio of active to inactive forms of acyl carrier protein in Escherichia coli by Jackowski (1983)10.1128/jb.166.3.866-871.1986
/ J Bacteriol / Consequences of reduced intracellular coenzyme A content in Escherichia coli by Jackowski (1986)10.1074/jbc.C109.002410
/ J Biol Chem / Acyl-acyl carrier protein regulates transcription of fatty acid biosynthetic genes via the FabT repressor in Streptococcus pneumoniae by Jerga (2009)10.1016/S1534-5807(03)00123-0
/ Dev Cell / FapR, a bacterial transcription factor involved in global regulation of membrane lipid biosynthesis by Schujman (2003)10.1007/s00203-005-0759-8
/ Arch Microbiol / The Bacillus subtilis desaturase: a model to understand phospholipid modification and temperature sensing by Mansilla (2005)-
Seltmann G, Holst O. The outer membrane Gram-negative bacteria, The bacterial cell wall, Springer; 2002. p. 18–22.
(
10.1007/978-3-662-04878-8
) 10.1128/JB.181.22.7028-7033.1999
/ J Bacteriol / Transcriptional control of the low-temperature-inducible des gene, encoding the D5 desaturase of Bacillus subtilis by Aguilar (1999)10.1074/jbc.M405150200
/ J Biol Chem / Bacillus subtilis DesR functions as a phosphorylation-activated switch to control membrane lipid fluidity by Cybulski (2004)10.1046/j.1365-2958.2002.03103.x
/ Mol Microbiol / Mechanism of membrane fluidity optimization: isothermal control of the Bacillus subtilis acyl-lipid desaturase by Cybulski (2002)10.1093/emboj/20.7.1681
/ EMBO J / Molecular basis of thermosensing: a two-component signal transduction thermometer in Bacillus subtilis by Aguilar (2001)10.1016/j.bbagen.2009.07.002
/ Biochim Biophys Acta / Oligomerization of Bacillus subtilis DesR is required for fine tuning regulation of membrane fluidity by Najle (2009)10.1128/JB.186.9.2655-2663.2004
/ J Bacteriol / The membrane fluidity sensor DesK of Bacillus subtilis controls the signal decay of its cognate response regulator by Albanesi (2004)10.1128/AEM.00882-08
/ Appl Environ Microbiol / Insertional inactivation of branched-chain α-keto acid dehydrogenase in Staphylococcus aureus leads to decreased branched-chain membrane fatty acid content and increased susceptibility to certain stresses by Singh (2008)10.1128/JB.00826-10
/ J Bacteriol / Transcriptomic and phenotypic characterization of a Bacillus subtilis strain without extracytoplasmic function sigma factors by Luo (2010)10.1371/journal.pone.0048471
/ PLoS ONE / Definition of the σW regulon of Bacillus subtilis in the absence of stress by Zweers (2012)10.1128/AEM.01560-09
/ Appl Environ Microbiol / Stress-responsive systems set specific limits to the overproduction of membrane proteins in Bacillus subtilis by Zweers (2009)10.1046/j.1365-2958.1999.01180.x
/ Mol Microbiol / Identification of target promoters for the Bacillus subtilis extracytoplasmic function sigma factor, σW by Huang (1999)10.1111/j.1365-2958.2011.07679.x
/ Mol Microbiol / A σW-dependent stress response in Bacillus subtilis that reduces membrane fluidity by Kingston (2011)10.1111/j.1365-2958.2007.06090.x
/ Mol Microbiol / The Bacillus subtilis σW regulon and its contribution to cell envelope stress responses by Eiamphungporn (2008)10.1128/JB.187.21.7444-7459.2005
/ J Bacteriol / Regulation of the pspA virulence factor and essential pcsB murein biosynthetic genes by the phosphorylated VicR (YycF) response regulator in Streptococcus pneumoniae by Ng (2005)10.1128/JB.01690-09
/ J Bacteriol / Kinetic characterization of the WalRKSpn (VicRK) two-component system of Streptococcus pneumoniae: dependence of WalKSpn (VicK) phosphatase activity on its PAS domain by Gutu (2010)10.1128/JB.186.4.1136-1146.2004
/ J Bacteriol / The Bacillus subtilis extracytoplasmic-function σX factor regulates modification of the cell envelope and resistance to cationic antimicrobial peptides by Cao (2004)10.1016/j.mib.2012.01.001
/ Curr Opin Microbiol / Extra cytoplasmic function sigma factor activation by Ho (2012)10.1126/science.274.5295.2107
/ Science / A mechanism of drug action revealed by structural studies of enoyl reductase by Baldock (1996)10.1074/jbc.275.4.2520
/ J Biol Chem / Action mechanism of antitubercular isoniazid. Activation by Mycobacterium tuberculosis KatG, isolation, and characterization of InhA inhibitor by Lei (2000)10.1038/18803
/ Nature (London) / Molecular basis of triclosan activity by Levy (1999)10.1074/jbc.274.16.11110
/ J Biol Chem / Mechanism of triclosan inhibition of bacterial fatty acid synthesis by Heath (1999)10.1002/jat.1660
/ J Appl Toxicol / Triclosan: environmental exposure, toxicity and mechanisms of action by Dann (2011)10.1128/AAC.47.12.3859-3866.2003
/ Antimicrob Agents Chemother / Triclosan as a systemic antibacterial agent in a mouse model of acute bacterial challenge by Sharma (2003)10.1089/mdr.2006.12.83
/ Microb Drug Resist / Triclosan and antimicrobial resistance in bacteria: an overview by Yazdankhah (2006)10.1038/nature08667
/ Nature (London) / Essentiality of FASII pathway for Staphylococcus aureus by Balemans (2010)10.1038/nrmicro2200
/ Nat Rev Microbiol / Waves of resistance: Staphylococcus aureus in the antibiotic era by Chambers (2009)10.1128/AAC.00012-06
/ Antimicrob Agents Chemother / Novel bacterial acetyl-coenzyme A carboxylase inhibitors with antibiotic efficacy in vivo by Freiberg (2006)10.1038/nature04784
/ Nature (London) / Platensimycin is a selective FabF inhibitor with potent antibiotic properties by Wang (2006)10.1128/AAC.46.10.3118-3124.2002
/ Antimicrob Agents Chemother / Discovery of a novel and potent class of FabI-directed antibacterial agents by Payne (2002)10.1021/jm020050+
/ J Med Chem / Discovery of aminopyridine-based inhibitors of bacterial enoyl-ACP reductase (FabI) by Miller (2002)10.1073/pnas.0700746104
/ Proc Natl Acad Sci USA / Discovery of platencin, a dual FabF and FabH inhibitor with in vivo antibiotic properties by Wang (2007)10.1128/AAC.01411-12
/ Antimicrob Agents Chemother / Mode of action, in vitro activity, and in vivo efficacy of AFN-1252, a selective antistaphylococcal FabI inhibitor by Kaplan (2012)10.1093/jac/dki123
/ J Antimicrob Chemother / Triclosan inhibition of fatty acid synthesis and its effect on growth of Escherichia coli and Pseudomonas aeruginosa by Escalada (2005)10.1086/381972
/ Clin Infect Dis / Clinical relevance of bacteriostatic versus bactericidal mechanisms of action in the treatment of Gram-positive bacterial infections by Pankey (2004)10.1128/AAC.00400-09
/ Antimicrob Agents Chemother / AFN-1252, a FabI inhibitor, demonstrates a Staphylococcal-specific spectrum of activity by Karlowsky (2009)10.1128/AAC.01254-06
/ Antimicrob Agents Chemother / In vitro activity of API-1252, a novel FabI inhibitor, against clinical isolates of Staphylococcus aureus and Staphylococcus epidermidis by Karlowsky (2007)10.1128/AAC.01248-10
/ Antimicrob Agents Chemother / The MUT056399 inhibitor of FabI is a new antistaphylococcal compound by Escaich (2011)10.1016/j.ijantimicag.2007.07.006
/ Int J Antimicrob Agents / CG400462, a new bacterial enoyl-acyl carrier protein reductase (FabI) inhibitor by Park (2007)10.1021/ar700156e
/ Acc Chem Res / Inhibitors of FabI, an enzyme drug target in the bacterial fatty acid biosynthesis pathway by Lu (2008)10.1038/nature07772
/ Nature (London) / Type II fatty acid synthesis is not a suitable antibiotic target for Gram-positive pathogens by Brinster (2009)10.1111/j.1365-2958.2011.07597.x
/ Mol Microbiol / A novel two-gene requirement for the octanoyltransfer reaction of Bacillus subtilis lipoic acid biosynthesis by Martin (2011)10.1126/science.1061217
/ Science / Complete genome sequence of a virulent isolate of Streptococcus pneumoniae by Tettelin (2001)10.1038/nature08668
/ Nature (London) / Brinster et al. reply by Brinster S (2010)10.1016/S0378-4347(00)83435-0
/ J Chromatogr / Quantitative determination of the fatty acid composition of human serum lipids by high-performance liquid chromatography by Shimomura (1986)
Dates
Type | When |
---|---|
Created | 12 years, 5 months ago (March 14, 2013, 3:07 p.m.) |
Deposited | 3 years, 6 months ago (Feb. 11, 2022, 3:52 a.m.) |
Indexed | 31 minutes ago (Aug. 27, 2025, 7:19 p.m.) |
Issued | 12 years, 1 month ago (July 1, 2013) |
Published | 12 years, 1 month ago (July 1, 2013) |
Published Print | 12 years, 1 month ago (July 1, 2013) |
@article{Parsons_2013, title={Bacterial lipids: Metabolism and membrane homeostasis}, volume={52}, ISSN={0163-7827}, url={http://dx.doi.org/10.1016/j.plipres.2013.02.002}, DOI={10.1016/j.plipres.2013.02.002}, number={3}, journal={Progress in Lipid Research}, publisher={Elsevier BV}, author={Parsons, Joshua B. and Rock, Charles O.}, year={2013}, month=jul, pages={249–276} }