High-Level Production of Indole-3-acetic Acid in the Metabolically Engineered Escherichia coil

被引:22
|
作者
Wu, Hongxuan [1 ]
Yang, Jinhua [1 ]
Shen, Peijie [1 ]
Li, Qingchen [2 ,3 ]
Wu, Weibin [4 ]
Jiang, Xianzhang [1 ]
Qin, Lina [1 ]
Huang, Jianzhong [1 ]
Cao, Xiao [4 ]
Qi, Feng [1 ]
机构
[1] Fujian Normal Univ, Coll Life Sci, Engn Res Ctr Ind Microbiol Minist Educ, Fuzhou 350117, Fujian, Peoples R China
[2] Fujian Normal Univ, Prov Univ Key Lab Cellular Stress Response & Meta, Fuzhou 350117, Fujian, Peoples R China
[3] Fujian Normal Univ, Prov Univ Engn Res Ctr Ind Biocatalysis, Fuzhou 350117, Fujian, Peoples R China
[4] Fujian Vocat Coll Bioengn, Fuzhou 350002, Fujian, Peoples R China
基金
中国国家自然科学基金;
关键词
indole-3-acetic acid; TAM; IAM; whole-cell catalysis; de novo biosynthesis;
D O I
10.1021/acs.jafc.0c08141
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Indole-3-acetic acid (IAA) is a critical plant hormone that regulates cell division, development, and metabolism. IAA synthesis in plants and plant-associated microorganisms cannot fulfill the requirement for large-scale agricultural production. Here, two novel IAA biosynthesis pathways, tryptamine (TAM) and indole-3-acetamide (IAM), were developed for IAA production by whole-cell catalysis and de novo biosynthesis in an engineered Escherichia coli MG1655. When 10 g/L l-tryptophan was used as a substrate, an MIA-6 strain containing a heterologous IAM pathway had the highest IAA titer of 7.10 g/L (1.34 x 10(3) mg/g DCW), which was 98.4 times more than MTAI-5 containing the TAM pathway by whole-cell catalysis. De novo IAA biosynthesis was optimized by improving NAD(P)H availability, resulting in an increased IAA titer of 906 mg/L obtained by the MG Delta adhE::icd strain, which is 29.7% higher than the control. These strategies exhibit the potential for IAA production in engineered E. coli and possible industrial applications.
引用
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页码:1916 / 1924
页数:9
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