Fermentative Indole Production via Bacterial Tryptophan Synthase Alpha Subunit and Plant Indole-3-Glycerol Phosphate Lyase Enzymes

被引:22
|
作者
Ferrer, Lenny [1 ]
Mindt, Melanie [2 ,3 ]
Suarez-Diez, Maria [4 ]
Jilg, Tatjana [1 ]
Zagorscak, Maja [5 ]
Lee, Jin-Ho [6 ]
Gruden, Kristina
Wendisch, Volker F. [1 ]
Cankar, Katarina [2 ,5 ]
机构
[1] Bielefeld Univ, Fac Biol & CeBiTec, Genet Prokaryotes, D-33615 Bielefeld, Germany
[2] Wageningen Univ & Res, Wageningen Plant Res, NL-6708PB Wageningen, Netherlands
[3] Axxence Aromat GmbH, D-46446 Emmerich Rhein, Germany
[4] Wageningen Univ Res, Lab Syst & Synthet Biol, NL-6708WE Wageningen, Netherlands
[5] Natl Inst Biol, Dept Biotechnol & Syst Biol, Ljubljana 1000, Slovenia
[6] Kyungsung Univ, Dept Food Sci & Biotechnol, Busan 608736, South Korea
基金
荷兰研究理事会;
关键词
Corynebacterium glutamicum; indole; indole-3-glycerol phosphate lyase; tryptophan synthase ?-subunit; bioprospecting; fermentative production; CORYNEBACTERIUM-GLUTAMICUM; ESCHERICHIA-COLI; MECHANISM; GENE; BIOSYNTHESIS; CATALYSIS; EMISSION; COMPLEX; CLONING; STATE;
D O I
10.1021/acs.jafc.2c01042
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Indole is produced in nature by diverse organisms and exhibits a characteristic odor described as animal, fecal, and floral. In addition, it contributes to the flavor in foods, and it is applied in the fragrance and flavor industry. In nature, indole is synthesized either from tryptophan by bacterial tryptophanases (TNAs) or from indole-3-glycerol phosphate (IGP) by plant indole-3-glycerol phosphate lyases (IGLs). While it is widely accepted that the tryptophan synthase alpha-subunit (TSA) has intrinsically low IGL activity in the absence of the tryptophan synthase beta-subunit, in this study, we show that Corynebacterium glutamicum TSA functions as a bona fide IGL and can support fermentative indole production in strains providing IGP. By bioprospecting additional bacterial TSAs and plant IGLs that function as bona fide IGLs were identified. Capturing indole in an overlay enabled indole production to titers of about 0.7 g L-1 in fermentations using C. glutamicum strains expressing either the endogenous TSA gene or the IGL gene from wheat.
引用
收藏
页码:5634 / 5645
页数:12
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