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Efficient Bioproduction of Indigo and Indirubin by Optimizing a Novel Terpenoid Cyclase XiaI in Escherichia coli

[Image: see text] Blue indigo dye, an important natural colorant, is used for textiles and food additives worldwide, while another red isomer, indirubin, is the major active ingredient of a traditional Chinese medicine named “Danggui Longhui Wan” for treating various diseases including granulocytic...

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Autores principales: Yin, Huifang, Chen, Hongping, Yan, Meng, Li, Zhikun, Yang, Rongdi, Li, Yanjiao, Wang, Yanfang, Guan, Jianyi, Mao, Huili, Wang, Yan, Zhang, Yuyang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8359145/
https://www.ncbi.nlm.nih.gov/pubmed/34396002
http://dx.doi.org/10.1021/acsomega.1c02679
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author Yin, Huifang
Chen, Hongping
Yan, Meng
Li, Zhikun
Yang, Rongdi
Li, Yanjiao
Wang, Yanfang
Guan, Jianyi
Mao, Huili
Wang, Yan
Zhang, Yuyang
author_facet Yin, Huifang
Chen, Hongping
Yan, Meng
Li, Zhikun
Yang, Rongdi
Li, Yanjiao
Wang, Yanfang
Guan, Jianyi
Mao, Huili
Wang, Yan
Zhang, Yuyang
author_sort Yin, Huifang
collection PubMed
description [Image: see text] Blue indigo dye, an important natural colorant, is used for textiles and food additives worldwide, while another red isomer, indirubin, is the major active ingredient of a traditional Chinese medicine named “Danggui Longhui Wan” for treating various diseases including granulocytic leukemia, cancer, and Alzheimer’s disease. In this work, we constructed a new and highly efficient indigoid production system by optimizing a novel terpenoid cyclase, XiaI, from the xiamycin biosynthetic pathway. Through introducing the flavin-reducing enzyme Fre, tryptophan-lysing and -importing enzymes TnaA and TnaB, and H(2)O(2)-degrading enzyme KatE and optimizing the fermentation parameters including temperature, the concentration of isopropyl-β-d-thiogalactopyranoside, and feeding of the l-tryptophan precursor, the final maximum productivity of indigoids by the recombinant strain Escherichia coli BL21(DE3) (XiaI-Fre-TnaAB-KatE) was apparently improved to 101.9 mg/L, an approximately 60-fold improvement to that of the starting strain E. coli BL21(DE3) (XiaI) (1.7 mg/L). In addition, when the fermentation system was enlarged to 1 L in the flask (feeding with 5 mM tryptophan and 10 mM 2-hydroxyindole), the indigoid productivity further increased to 276.7 mg/L at 48 h, including an indigo productivity of 26.0 mg/L and an indirubin productivity of 250.7 mg/L, which has been the highest productivity of indirubin so far. This work provided a basis for the commercial production of bio-indigo and the clinical drug indirubin in the future.
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spelling pubmed-83591452021-08-13 Efficient Bioproduction of Indigo and Indirubin by Optimizing a Novel Terpenoid Cyclase XiaI in Escherichia coli Yin, Huifang Chen, Hongping Yan, Meng Li, Zhikun Yang, Rongdi Li, Yanjiao Wang, Yanfang Guan, Jianyi Mao, Huili Wang, Yan Zhang, Yuyang ACS Omega [Image: see text] Blue indigo dye, an important natural colorant, is used for textiles and food additives worldwide, while another red isomer, indirubin, is the major active ingredient of a traditional Chinese medicine named “Danggui Longhui Wan” for treating various diseases including granulocytic leukemia, cancer, and Alzheimer’s disease. In this work, we constructed a new and highly efficient indigoid production system by optimizing a novel terpenoid cyclase, XiaI, from the xiamycin biosynthetic pathway. Through introducing the flavin-reducing enzyme Fre, tryptophan-lysing and -importing enzymes TnaA and TnaB, and H(2)O(2)-degrading enzyme KatE and optimizing the fermentation parameters including temperature, the concentration of isopropyl-β-d-thiogalactopyranoside, and feeding of the l-tryptophan precursor, the final maximum productivity of indigoids by the recombinant strain Escherichia coli BL21(DE3) (XiaI-Fre-TnaAB-KatE) was apparently improved to 101.9 mg/L, an approximately 60-fold improvement to that of the starting strain E. coli BL21(DE3) (XiaI) (1.7 mg/L). In addition, when the fermentation system was enlarged to 1 L in the flask (feeding with 5 mM tryptophan and 10 mM 2-hydroxyindole), the indigoid productivity further increased to 276.7 mg/L at 48 h, including an indigo productivity of 26.0 mg/L and an indirubin productivity of 250.7 mg/L, which has been the highest productivity of indirubin so far. This work provided a basis for the commercial production of bio-indigo and the clinical drug indirubin in the future. American Chemical Society 2021-07-27 /pmc/articles/PMC8359145/ /pubmed/34396002 http://dx.doi.org/10.1021/acsomega.1c02679 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Yin, Huifang
Chen, Hongping
Yan, Meng
Li, Zhikun
Yang, Rongdi
Li, Yanjiao
Wang, Yanfang
Guan, Jianyi
Mao, Huili
Wang, Yan
Zhang, Yuyang
Efficient Bioproduction of Indigo and Indirubin by Optimizing a Novel Terpenoid Cyclase XiaI in Escherichia coli
title Efficient Bioproduction of Indigo and Indirubin by Optimizing a Novel Terpenoid Cyclase XiaI in Escherichia coli
title_full Efficient Bioproduction of Indigo and Indirubin by Optimizing a Novel Terpenoid Cyclase XiaI in Escherichia coli
title_fullStr Efficient Bioproduction of Indigo and Indirubin by Optimizing a Novel Terpenoid Cyclase XiaI in Escherichia coli
title_full_unstemmed Efficient Bioproduction of Indigo and Indirubin by Optimizing a Novel Terpenoid Cyclase XiaI in Escherichia coli
title_short Efficient Bioproduction of Indigo and Indirubin by Optimizing a Novel Terpenoid Cyclase XiaI in Escherichia coli
title_sort efficient bioproduction of indigo and indirubin by optimizing a novel terpenoid cyclase xiai in escherichia coli
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8359145/
https://www.ncbi.nlm.nih.gov/pubmed/34396002
http://dx.doi.org/10.1021/acsomega.1c02679
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