1973•Canadian Journal of BiochemistryRequires access

Biochemistry of Polyglycerophosphatides. The Mechanism of Cardiolipin Biosynthesis in Isolated Mitochondria

N. Ž. Stanaćev, J. B. Davidson, Lidija Stuhne-sekalec, Z. Domazet

Open publisher page 27 citations

Abstract

The mechanism of cardiolipin biosynthesis in isolated rat liver mitochondria was studied using endogenously formed and exogenously supplied phosphatidylglycerol-2′-3H in the presence and absence of added Mg2+, Mn2+, CDP-DL-dioleate, and CDP-D-diglyceride-2-14C. With endogenously formed and membrane-bound phosphatidylglycerol-2′-3H and in the presence of Mn2+, the incorporation of CDP-D-diglyceride-2-14C into cardiolipin-3H,14C was demonstrated, establishing the participation of both phosphatidylglycerol-2′-3H and CDP-D-diglyceride-2-14C in the formation of cardiolipin-3H,14C. In addition, the release of water-soluble labeled compounds was measured and the efficiency of glycerol-2-3H recovery after the incubation with mitochondria was determined. It was concluded that under the described experimental conditions the formation of cardiolipin in isolated mitochondria takes place according to the reaction mechanism: phosphatidylglycerol + CDP-diglyceride → cardiolipin. Some aspects of these findings are discussed in detail

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The mechanism of cardiolipin biosynthesis in isolated rat liver mitochondria was studied using endogenously formed and exogenously supplied phosphatidylglycerol-2′-3H in the presence and absence of added Mg2+, Mn2+, CDP-DL-dioleate, and CDP-D-diglyceride-2-14C. With endogenously formed and membrane-bound phosphatidylglycerol-2′-3H and in the presence of Mn2+, the incorporation of CDP-D-diglyceride-2-14C into cardiolipin-3H,14C was demonstrated, establishing the participation of both phosphatidylglycerol-2′-3H and CDP-D-diglyceride-2-14C in the formation of cardiolipin-3H,14C. In addition, the release of water-soluble labeled compounds was measured and the efficiency of glycerol-2-3H recovery after the incubation with mitochondria was determined. It was concluded that under the described experimental conditions the formation of cardiolipin in isolated mitochondria takes place according to the reaction mechanism: phosphatidylglycerol + CDP-diglyceride → cardiolipin. Some aspects of these findings are discussed in detail

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Available abstract

The mechanism of cardiolipin biosynthesis in isolated rat liver mitochondria was studied using endogenously formed and exogenously supplied phosphatidylglycerol-2′-3H in the presence and absence of added Mg2+, Mn2+, CDP-DL-dioleate, and CDP-D-diglyceride-2-14C. With endogenously formed and membrane-bound phosphatidylglycerol-2′-3H and in the presence of Mn2+, the incorporation of CDP-D-diglyceride-2-14C into cardiolipin-3H,14C was demonstrated, establishing the participation of both phosphatidylglycerol-2′-3H and CDP-D-diglyceride-2-14C in the formation of cardiolipin-3H,14C. In addition, the release of water-soluble labeled compounds was measured and the efficiency of glycerol-2-3H recovery after the incubation with mitochondria was determined. It was concluded that under the described experimental conditions the formation of cardiolipin in isolated mitochondria takes place according to the reaction mechanism: phosphatidylglycerol + CDP-diglyceride → cardiolipin. Some aspects of these findings are discussed in detail

Key concepts: Cardiolipin, Phosphatidylglycerol, Biochemistry, Biosynthesis, Diglyceride, Glycerol, Mitochondrion, Chemistry

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