Structural characterization of the polar lipids of Clostridium novyi NT. Further evidence for a novel anaerobic biosynthetic pathway to plasmalogens
A study of the polar lipids of Clostridium novyi NT has revealed the presence of phosphatidylethanolamine (PE) and cardiolipin as major phospholipids with smaller amounts of phosphatidylglycerol (PG), lysyl-PG and alanyl-PG. Other minor phospholipids included phosphatidic acid, CDP-diacylglycerol, p...
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Published in | Biochimica et biophysica acta Vol. 1811; no. 3; pp. 186 - 193 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Netherlands
Elsevier B.V
01.03.2011
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Subjects | |
Online Access | Get full text |
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Summary: | A study of the polar lipids of
Clostridium novyi NT has revealed the presence of phosphatidylethanolamine (PE) and cardiolipin as major phospholipids with smaller amounts of phosphatidylglycerol (PG), lysyl-PG and alanyl-PG. Other minor phospholipids included phosphatidic acid, CDP-diacylglycerol, phosphatidylserine (PS) and phosphatidylthreonine (PT). PE, PG and amino acyl PG were present in both the diacyl and alk-1′-enyl acyl (plasmalogen) forms and cardiolipin plasmalogens were found to contain one or two alk-1′-enyl chains. In contrast, the precursor lipids phosphatidic acid, CDP-diacylglycerol and PS were present almost exclusively as diacyl phospholipids. These findings are consistent with the hypothesis that plasmalogens are formed from diacylated phospholipids at a late stage of phospholipid formation in
Clostridium species. This novel pathway contrasts with the route in animals in which a saturated ether bond is formed at an early stage of plasmalogen biosynthesis and the alk-1-enyl bond is formed by an aerobic mechanism.
► The lipidome of
Clostridium novyi is presented for the first time. ► The end-products of lipid biosynthesis are found in all acyl or plasmalogen species. ► The intermediates of phospholipid biosynthesis contain very little plasmalogen form. ► Plasmalogens in clostridia are formed from the corresponding all acyl lipids. |
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Bibliography: | http://dx.doi.org/10.1016/j.bbalip.2010.12.010 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1388-1981 0006-3002 1879-2618 |
DOI: | 10.1016/j.bbalip.2010.12.010 |