Anaplerotic carboxylation refers the linkage reactions between glycolysis and TCA cycle mediating carboxylation of C3 metabolites into C4 metabolites. The energy for carbon-carbon bondage formation derives from difference sources in the anaplerotic enzymes, and the artificial anaplerotic carboxylation was affected by intracellular modulating metabolite concentrations, cofactors(3), and the way of regulations(2). Artificial expression of anaplerotic enzymes such as phosphoenolpyruvate carboxylase(PPC), phosphoenolpyruvate carboxykinase(PCK), and NADP-dependent malic enzyme(MaeB) enhanced the carboxylation of C3 metabolites under anaerobic with surplus of CO2 source (119 mM bicarbonate) conditions(4). The availability of CO2 source for the anaplerotic enzymes were corelated to the C4 metabolite production(5). The NAD-dependent Malic enzyme(MaeA) expression mediated decarboxylation under the same conditions. Cellular energy currencies related to the anaplerotic enzyme expressions were modified depending on their chemical energy source for carboxylation, i.e., PEP for PPC, PEP and ATP for PCK, NADPH for MaeB, and NADH for MaeA, and on their modulating metabolite concentrations. The examples of cellular energy currency modifications are introduced as well as the cellular responses therefrom(1, 6).
한국생물공학회 [The Korean Society for Biotechnology and Bioengineering]
설립연도
1984
분야
공학>생물공학
소개
이 법인은 생물 공학의 발전과 보급에 이바지하고, 회원 상호 간의 연구 협력과 친목을 도모함을 목적으로 한다
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