Fig. 1From: High-yield anaerobic succinate production by strategically regulating multiple metabolic pathways based on stoichiometric maximum in Escherichia coli Metabolic network of E. coli under anaerobic conditions and metabolic engineering strategies for succinate overproduction. Modified genes for improving succinate yield are highlighted in bold. X indicates metabolic reactions that have been blocked by gene deletions. Dotted arrows indicate steps that are heterogeneously expressed in E. coli. Genes and enzymes: ldhA encoding lactate dehydrogenase; pflB encoding pyruvate-formate lyase; pta encoding phosphate acetyltransferase; ackA encoding acetate kinase; adhE encoding alcohol dehydrogenase; ppc encoding phosphoenolpyruvate carboxylase; pepck encoding phosphoenolpyruvate carboxykinase; pyc encoding pyruvate carboxylase; aceEF-lpd encoding pyruvate dehydrogenase complex; mdh encoding malate dehydrogenase; fumA, fumB, and fumC encoding fumarase isozymes; frdABCD encoding fumarate reductase; galp encoding galactose permease; glk encoding glucokinase; PTS phosphotransferase systems; zwf243 encoding 6-phosphate dehydrogenase; gnd361 encoding 6-phosphogluconate dehydrogenase; pgl encoding 6-phosphogluconolactonase; tktA encoding transketolase; talB encoding transaldolase; sthA encoding soluble transhydrogenaseBack to article page