Abstract

In order to reduce acetate production and improve succinate production and explore the main acetate formation pathways of C.acetoacidophilum,gene of pta,ackA,ctfA and aceE,which encoded phosphotransacetylase,acetate kinase,CoA-transfease and pyruvate dehydrogenase complex in C.acetoacidophilum were disrupted respectively by the means of homologous recombination.In C.acetoacidophilum△ldhA△pta-ackA,the titer of acetate,gluocse consumption rate,and both yields of acetate and succinate were found to be similar to that of C.acetoacidophilum AldhA.Furthermore,the titer and yield of acetate decreased by81.4%and 77.2%,respectively,the glucose consumption rate decreased by 28.3%and the yield of succinate increased by 25.3%in C.acetoacidophilum △ldhA△ctfA△pta-ackA.In addition,when gene aceE was deleted,C.acetoacidophilum △ldhA△aceE almost produced no acetate,the glucose consumption rate decrease by 35.6%and the yield of succinate increased by 34.7%.Under oxygen deprivation,almost all acetate formed through acetyl-CoA in C.acetoacidophilum.Gene pta,ackA and ctfA were the main genes of acetate formation pathways from acetyl-CoA.Disrupting gene aceE could cut off acetate synthesis in C.acetoacidophilum,and effectively increase succinate production.

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