Fatty Aldehydes in Cyanobacteria Are a Metabolically Flexible Precursor for a Diversity of Biofuel Products

被引:51
|
作者
Kaiser, Brett K. [1 ]
Carleton, Michael [1 ]
Hickman, Jason W. [1 ]
Miller, Cameron [1 ]
Lawson, David [1 ]
Budde, Mark [1 ]
Warrener, Paul [1 ]
Paredes, Angel [3 ]
Mullapudi, Srinivas [3 ]
Navarro, Patricia [3 ]
Cross, Fred [4 ]
Roberts, James M. [2 ,5 ]
机构
[1] Matrix Genet, Seattle, WA USA
[2] Univ Washington, Dept Biochem, Seattle, WA 98195 USA
[3] Univ Texas Hlth Sci Ctr, Dept Pathol & Lab Med, Houston, TX USA
[4] Rockefeller Univ, New York, NY 10021 USA
[5] Fred Hutchinson Canc Res Ctr, Div Basic Sci, Seattle, WA 98104 USA
来源
PLOS ONE | 2013年 / 8卷 / 03期
关键词
ACYL CARRIER PROTEIN; ESCHERICHIA-COLI; DEHYDROGENASE GENES; LIPID-PEROXIDATION; ACID SYNTHESIS; WAX ESTER; PURIFICATION; EXPRESSION; COENZYME; BIOSYNTHESIS;
D O I
10.1371/journal.pone.0058307
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We describe how pathway engineering can be used to convert a single intermediate derived from lipid biosynthesis, fatty aldehydes, into a variety of biofuel precursors including alkanes, free fatty acids and wax esters. In cyanobacteria, long-chain acyl-ACPs can be reduced to fatty aldehydes, and then decarbonylated to alkanes. We discovered a cyanobacteria class-3 aldehyde-dehydrogenase, AldE, that was necessary and sufficient to instead oxidize fatty aldehyde precursors into fatty acids. Overexpression of enzymes in this pathway resulted in production of 50 to 100 fold more fatty acids than alkanes, and the fatty acids were secreted from the cell. Co-expression of acyl-ACP reductase, an alcohol-dehydrogenase and a wax-ester-synthase resulted in a third fate for fatty aldehydes: conversion to wax esters, which accumulated as intracellular lipid bodies. Conversion of acyl-ACP to fatty acids using endogenous cyanobacterial enzymes may allow biofuel production without transgenesis.
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页数:11
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