BioChem - DOS

Adenosine triphosphate and carbon efficient route to second generation biofuel isopentanol

ACS Synthetic biology

Eiben, Christopher B.; Tian, Tian; Thompson, Mitchell G.; Mendez-Perez, Daniel; Kaplan, Nurgul; Goyal, Garima; Chiniquy, Jennifer; Hillson, Nathan J.; Lee, Taek Soon; Keasling, Jay D.

<P>Climate change necessitates the development of CO<SUB>2</SUB> neutral or negative routes to chemicals currently produced from fossil carbon. In this paper we demonstrate a pathway from the renewable resource glucose to next generation biofuel isopentanol by pairing the isovaleryl-CoA biosynthesis pathway from <I>Myxococcus xanthus</I> and a butyryl-CoA reductase from <I>Clostridium acetobutylicum</I>. The best plasmid and <I>Escherichia coli</I> strain combination makes 80.50 ± 8.08 (SD) mg/L of isopentanol after 36 h under microaerobic conditions with an oleyl alcohol overlay. In addition, the system also shows a strong preference for isopentanol production over prenol in microaerobic conditions. Finally, the pathway requires zero adenosine triphosphate and can be paired theoretically with nonoxidative glycolysis, the combination being redox balanced from glucose thus avoiding unnecessary carbon loss as CO<SUB>2</SUB>. These pathway properties make the isovaleryl-CoA pathway an attractive isopentanol production route for further optimization.</P><BR>[FIG OMISSION]</BR>

2020

American Chemical Society

2161-5063

9

3

pp.468-474

10.1021/acssynbio.9b00402.s002

http://click.ndsl.kr/servlet/OpenAPIDetailView?keyValue=05787966&target=NART&cn=NART99580842

https://escholarship.org/content/qt7m25c4wc/qt7m25c4wc.pdf?t=q7c3r8

isopentanol; isovaleryl-CoA pathway; biofuel