1975
DOI: 10.1016/0014-5793(75)80995-1
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The role of phosphatidylglycerol in the in vitro biosynthesis of teichoic acid and lipoteichoic acid

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Cited by 51 publications
(29 citation statements)
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“…In Enterococccus hirae ATCC 9790, Gro-P moieties are added sequentially to the glycolipid acceptor, phosphatidylkojibiosyldiacylglycerol (176). This observation is consistent with the in vivo pulse-chase experiments that implicated phosphatidylglycerol as the donor of Gro-P units (147,185). On the other hand, the discovery of a series of oligophosphoglycerophospholipids derived from phosphatidylglycerol in Streptococcus sanguis suggested that these lipids may be intermediates in the assembly of LTA and that the mechanism of assembly may differ from that observed in E. hirae (92).…”
Section: Pathways Of Lta and Wta Biosynthesissupporting
confidence: 85%
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“…In Enterococccus hirae ATCC 9790, Gro-P moieties are added sequentially to the glycolipid acceptor, phosphatidylkojibiosyldiacylglycerol (176). This observation is consistent with the in vivo pulse-chase experiments that implicated phosphatidylglycerol as the donor of Gro-P units (147,185). On the other hand, the discovery of a series of oligophosphoglycerophospholipids derived from phosphatidylglycerol in Streptococcus sanguis suggested that these lipids may be intermediates in the assembly of LTA and that the mechanism of assembly may differ from that observed in E. hirae (92).…”
Section: Pathways Of Lta and Wta Biosynthesissupporting
confidence: 85%
“…For example, in organisms that have the repeating unit -Gro-P-for both LTA and WTA (such as B. subtilis 168), the units are derived from different sources. WTA contains sn-glycerol 3-phosphate derived from CDP-glycerol (78,201), whereas LTA contains snglycerol 1-phosphate derived from phosphatidylglycerol (147,176,315). Because of the different origins of the Gro-P units, the chains are not stereoisomerically identical.…”
Section: Pathways Of Lta and Wta Biosynthesismentioning
confidence: 99%
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“…This glycerol phosphate structure is conserved in many different Gram-positive bacteria including the human pathogens B. anthracis, Enterococcus faecalis, L. monocytogenes, S. agalactiae, and S. pyogenes (18,37). Biosynthesis of LTA has been studied with in vitro experiments using isolated bacterial membranes or toluene-treated cells (38,39). PG was demonstrated to function as substrate for LTA synthesis (39), whereas CDP glycerol, a sn-glycerol-3-phosphate and substrate for WTA assembly, cannot substitute during LTA synthesis (40).…”
Section: Discussionmentioning
confidence: 99%
“…Recently, it was shown that secretion of LTA in Lactobacillus casei was the result of continued phospholipid synthesis following cessation of growth and blebbing of the cytoplasmic membrane from the septum of these cells (35a). Enhanced or continued phospholipid synthesis would supply substrate for polymerization, since diphosphatidylglycerol has been shown to serve as the precursor in the polymerization of LTA (5,11).…”
Section: Methodsmentioning
confidence: 99%