초록
<P><I>Corynebacterium glutamicum</I> lacking the succinate dehydrogenase complex can produce succinate aerobically with acetate representing the major byproduct. Efforts to increase succinate production involved deletion of acetate formation pathways and overexpression of anaplerotic pathways, but acetate formation could not be completely eliminated. To address this issue, we constructed a pathway for recycling wasted carbon in succinate-producing <I>C. glutamicum</I>. The acetyl-CoA synthetase from <I>Bacillus subtilis</I> was heterologously introduced into <I>C. glutamicum</I> for the first time. The engineered strain ZX1 (pEacsA) did not secrete acetate and produced succinate with a yield of 0.50 mol (mol glucose)<SUP>−1</SUP>. Moreover, in order to drive more carbon towards succinate biosynthesis, the native citrate synthase encoded by <I>gltA</I> was overexpressed, leading to strain ZX1 (pEacsAgltA), which showed a 22% increase in succinate yield and a 62% decrease in pyruvate yield compared to strain ZX1 (pEacsA). In fed-batch cultivations, strain ZX1 (pEacsAgltA) produced 241 mM succinate with an average volumetric productivity of 3.55 mM h<SUP>−1</SUP> and an average yield of 0.63 mol (mol glucose) <SUP>−1</SUP>, making it a promising platform for the aerobic production of succinate at large scale.</P>