초록
<P><B>Abstract</B></P> <P>Biotechnological production of butanol in heterologous hosts has recently attracted many interests. Of the heterologous hosts investigated to date, engineered <I>Escherichia coli</I> has shown a superior butanol yield than the natural butanol-producing clostridial strains. However, all reported butanol-producing <I>E. coli</I> strains contain vectors and inducible promoters, which means antibiotics and inducers are required in the fermentation. The aim of this study was to develop a completely chromosomally engineered <I>E. coli</I> strain capable of producing butanol efficiently in the absence of vectors, antibiotics, and inducers. The challenges are the expression strength of chromosomally engineered genes under constitutive promoters is much weaker than the vector engineered genes under inducible promoters. To address these challenges, the butanol pathway was engineered into the chromosome in the first place, then the host and the butanol pathway was iteratively engineered through rational and non-rational strategies to develop an efficient butanol producer where the heterologous butanol pathway fits the host well. Finally, a systematically chromosomally engineered <I>E. coli</I> strain EB243, in which 33 native genes were deleted and 5 heterologous genes were introduced, was developed. Strain EB243 could produce 20g/L butanol with a yield of 34% (w/w, 83% of theoretical yield) in batch fermentation without any antibiotics and inducers, thus showed great potential for industrial application. This work also demonstrated a procedure on how to integrate the existing knowledge to engineer a strain with industrial application potential.</P> <P><B>Highlights</B></P> <P> <UL> <LI> A completely chromosomally engineered efficient butanol producing <I>E. coli</I> strain was developed. </LI> <LI> This <I>E. coli</I> strain could produce 20g/L butanol, with a mass yield of 34%, without adding any antibiotics or inducers. </LI> <LI> This is the first vector-free recombinant <I>E. coli</I> producing the highest titer of butanol without in situ removal of butanol. </LI> </UL> </P>