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Title: Effect of 3,4-dihydroxybutyl-1-phosphonate on cardiolipin synthesis in B. subtilis. Author: Lacombe C, Lubochinsky B. Journal: Biochim Biophys Acta; 1989 Sep 25; 1005(2):103-8. PubMed ID: 2550075. Abstract: Endogenous phosphatidylglycerol is rapidly transformed into cardiolipin when B. subtilis 168 cells were incubated in a buffer without an energy source. Upon addition of 3,4-dihydroxybutyl-1-phosphonate (DHBP), a synthetic glycerol 3-phosphate analogue, this synthesis was completely blocked after a short lag; if the cells were grown in the presence of the analogue, there was no lag. When membrane fractions were incubated with exogenous [32P]phosphatidylglycerol, free DHBP and glycerol 3-phosphate had no effect on [32P]cardiolipin synthesis, but phosphatidyl-DHBP and phosphatidylglycerolphosphate were potent inhibitors. These results are consistent with our hypothesis that phosphatidylglycerolphosphate, the phosphatidylglycerol precursor, might also be a physical inhibitor of cardiolipin synthesis.[Abstract] [Full Text] [Related] [New Search]