Fig. 5 | Nature Communications

Fig. 5

From: Metabolic engineering of Escherichia coli for de novo biosynthesis of vitamin B12

Fig. 5

Comparison of vitamin B12 production and growth in E. coli strains expressing Module 4 and 5. a Vitamin B12 production and growth of E. coli expressing the cobN,S,T genes from a single species (B. melitensis, S. meliloti or R. capsulatus) as well as the cobW gene from B. melitensis, S. meliloti, or R. capsulatus. b Vitamin B12 production and growth of E. coli strains expressing various combinations of the cobN, cobS, cobT, and cobW genes from B. melitensis, S. meliloti, or R. capsulatus. c Vitamin B12 production and growth of E. coli expressing different variant forms of Module 4. Bm, Sm, Rc, St, and Ec represent abbreviations of strains B. melitensis, S. meliloti, R. capsulatus, S. typhimurium, and E. coli, respectively. 1, 2, 3, 4, and 5 in Fig. 5c represent genes encoding cob(I)yrinic acid a,c-diamide adenosyltransferase, adenosylcobyric acid synthase, L-threonine kinase, threonine-O-3-phosphate decarboxylase, and AdoCbi-P synthase, respectively. All strains were cultured in CM medium for vitamin B12 production. Error bars indicate standard deviations from triplicate biological replicates

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