Elucidating acetate tolerance in E. coli using a genome-wide approach

被引:57
作者
Sandoval, Nicholas R. [1 ]
Mills, Tirzah Y. [1 ]
Zhang, Min [2 ]
Gill, Ryan T. [1 ]
机构
[1] Univ Colorado, Dept Chem & Biol Engn, Boulder, CO 80309 USA
[2] Natl Renewable Energy Lab, Golden, CO 80401 USA
基金
美国国家科学基金会;
关键词
Acetate; Directed evolution; Cellulosic feedstock; Genome library; Selection; DEPENDENT ACID RESISTANCE; ESCHERICHIA-COLI; AGMATINE ANTIPORTER; PH; PRETREATMENT; INHIBITION; ARGININE; GROWTH; LIPOPOLYSACCHARIDE; FERMENTATION;
D O I
10.1016/j.ymben.2010.12.001
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Engineering organisms for improved performance using lignocellulose feedstocks is an important step towards a sustainable fuel and chemical industry. Cellulosic feedstocks contain carbon and energy in the form of cellulosic and hemicellulosic sugars that are not metabolized by most industrial microorganisms. Pretreatment processes that hydrolyze these polysaccharides often also result in the accumulation of growth inhibitory compounds, such as acetate and furfural among others. Here, we have applied a recently reported strategy for engineering tolerance towards the goal of increasing Escherichia coli growth in the presence of elevated acetate concentrations (Lynch et al., 2007). We performed growth selections upon an E. coli genome library developed using a moderate selection pressure to identify genomic regions implicated in acetate toxicity and tolerance. These studies identified a range of high-fitness genes that are normally involved in membrane and extracellular processes, are key regulated steps in pathways, and are involved in pathways that yield specific amino acids and nucleotides. Supplementation of the products and metabolically related metabolites of these pathways significantly increased growth rate (a 130% increase in specific growth) at inhibitory acetate concentrations. Our results suggest that acetate tolerance will not involve engineering of a single pathway; rather we observe a range of potential mechanisms for overcoming acetate based inhibition. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:214 / 224
页数:11
相关论文
共 59 条
[1]  
Aden A., 2002, NATL RENEWABLE ENERG
[2]   Global transcription machinery engineering: A new approach for improving cellular phenotype [J].
Alper, Hal ;
Stephanopoulos, Gregory .
METABOLIC ENGINEERING, 2007, 9 (03) :258-267
[3]  
[Anonymous], 2012, Molecular Cloning: A Laboratory Manual
[4]  
[Anonymous], 2009, ANN EN OUTL 2009 PRO
[5]   Global analysis of Escherichia coli gene expression during the acetate-induced acid tolerance response [J].
Arnold, CN ;
McElhanon, J ;
Lee, A ;
Leonhart, R ;
Siegele, DA .
JOURNAL OF BACTERIOLOGY, 2001, 183 (07) :2178-2186
[6]   TRANSPORT OF LACTATE AND ACETATE THROUGH THE ENERGIZED CYTOPLASMIC MEMBRANE OF ESCHERICHIA-COLI [J].
AXE, DD ;
BAILEY, JE .
BIOTECHNOLOGY AND BIOENGINEERING, 1995, 47 (01) :8-19
[7]   Construction of Escherichia coli K-12 in-frame, single-gene knockout mutants:: the Keio collection [J].
Baba, Tomoya ;
Ara, Takeshi ;
Hasegawa, Miki ;
Takai, Yuki ;
Okumura, Yoshiko ;
Baba, Miki ;
Datsenko, Kirill A. ;
Tomita, Masaru ;
Wanner, Barry L. ;
Mori, Hirotada .
MOLECULAR SYSTEMS BIOLOGY, 2006, 2 (1) :2006.0008
[8]   In the light of directed evolution: Pathways of adaptive protein evolution [J].
Bloom, Jesse D. ;
Arnold, Frances H. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 :9995-10000
[9]   A comparative study of metabolic engineering anti-metabolite tolerance in Escherichia coli [J].
Bonomo, Jeanne ;
Warnecke, Tanya ;
Hume, Patrick ;
Marizcurrena, Alex ;
Gill, Ryan T. .
METABOLIC ENGINEERING, 2006, 8 (03) :227-239
[10]   A genomic-library based discovery of a novel, possibly synthetic, acid-tolerance mechanism in Clostridium acetobutylicum involving non-coding RNAs and ribosomal RNA processing [J].
Borden, Jacob R. ;
Jones, Shawn W. ;
Indurthi, Dinesh ;
Chen, Yili ;
Papoutsakis, Eleftherios Terry .
METABOLIC ENGINEERING, 2010, 12 (03) :268-281