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Cofactor engineering to regulate NAD(+)/NADH ratio with its application to phytosterols biotransformation

BACKGROUND: Cofactor engineering is involved in the modification of enzymes related to nicotinamide adenine dinucleotides (NADH and NAD(+)) metabolism, which results in a significantly altered spectrum of metabolic products. Cofactor engineering plays an important role in metabolic engineering but i...

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Autores principales: Su, Liqiu, Shen, Yanbing, Zhang, Wenkai, Gao, Tian, Shang, Zhihua, Wang, Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5663084/
https://www.ncbi.nlm.nih.gov/pubmed/29084539
http://dx.doi.org/10.1186/s12934-017-0796-4
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author Su, Liqiu
Shen, Yanbing
Zhang, Wenkai
Gao, Tian
Shang, Zhihua
Wang, Min
author_facet Su, Liqiu
Shen, Yanbing
Zhang, Wenkai
Gao, Tian
Shang, Zhihua
Wang, Min
author_sort Su, Liqiu
collection PubMed
description BACKGROUND: Cofactor engineering is involved in the modification of enzymes related to nicotinamide adenine dinucleotides (NADH and NAD(+)) metabolism, which results in a significantly altered spectrum of metabolic products. Cofactor engineering plays an important role in metabolic engineering but is rarely reported in the sterols biotransformation process owing to its use of multi-catabolic enzymes, which promote multiple consecutive reactions. Androst-4-ene-3, 17-dione (AD) and androst-1, 4-diene-3, 17-dione (ADD) are important steroid medicine intermediates that are obtained via the nucleus oxidation and the side chain degradation of phytosterols by Mycobacterium. Given that the biotransformation from phytosterols to AD (D) is supposed to be a NAD(+)-dependent process, this work utilized cofactor engineering in Mycobacterium neoaurum and investigated the effect on cofactor and phytosterols metabolism. RESULTS: Through the addition of the coenzyme precursor of nicotinic acid in the phytosterols fermentation system, the intracellular NAD(+)/NADH ratio and the AD (D) production of M. neoaurum TCCC 11978 (MNR M3) were higher than in the control. Moreover, the NADH: flavin oxidoreductase was identified and was supposed to exert a positive effect on cofactor regulation and phytosterols metabolism pathways via comparative proteomic profiling of MNR cultured with and without phytosterols. In addition, the NADH: flavin oxidoreductase and a water-forming NADH oxidase from Lactobacillus brevis, were successfully overexpressed and heterologously expressed in MNR M3 to improve the intracellular ratio of NAD(+)/NADH. After 96 h of cultivation, the expression of these two enzymes in MNR M3 resulted in the decrease in intracellular NADH level (by 51 and 67%, respectively) and the increase in NAD(+)/NADH ratio (by 113 and 192%, respectively). Phytosterols bioconversion revealed that the conversion ratio of engineered stains was ultimately improved by 58 and 147%, respectively. The highest AD (D) conversion ratio by MNR M3N2 was 94% in the conversion system with soybean oil as reaction media to promote the solubility of phytosterols. CONCLUSIONS: The ratio of NAD(+)/NADH is an important factor for the transformation of phytosterols. Expression of NADH: flavin oxidoreductase and water-forming NADH oxidase in MNR improved AD (D) production. Besides the manipulation of key enzyme activities, which included in phytosterols degradation pathways, maintenance the balance of redox also played an important role in promoting steroid biotransformation. The recombinant MNR strain may be useful in industrial production.
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spelling pubmed-56630842017-11-01 Cofactor engineering to regulate NAD(+)/NADH ratio with its application to phytosterols biotransformation Su, Liqiu Shen, Yanbing Zhang, Wenkai Gao, Tian Shang, Zhihua Wang, Min Microb Cell Fact Research BACKGROUND: Cofactor engineering is involved in the modification of enzymes related to nicotinamide adenine dinucleotides (NADH and NAD(+)) metabolism, which results in a significantly altered spectrum of metabolic products. Cofactor engineering plays an important role in metabolic engineering but is rarely reported in the sterols biotransformation process owing to its use of multi-catabolic enzymes, which promote multiple consecutive reactions. Androst-4-ene-3, 17-dione (AD) and androst-1, 4-diene-3, 17-dione (ADD) are important steroid medicine intermediates that are obtained via the nucleus oxidation and the side chain degradation of phytosterols by Mycobacterium. Given that the biotransformation from phytosterols to AD (D) is supposed to be a NAD(+)-dependent process, this work utilized cofactor engineering in Mycobacterium neoaurum and investigated the effect on cofactor and phytosterols metabolism. RESULTS: Through the addition of the coenzyme precursor of nicotinic acid in the phytosterols fermentation system, the intracellular NAD(+)/NADH ratio and the AD (D) production of M. neoaurum TCCC 11978 (MNR M3) were higher than in the control. Moreover, the NADH: flavin oxidoreductase was identified and was supposed to exert a positive effect on cofactor regulation and phytosterols metabolism pathways via comparative proteomic profiling of MNR cultured with and without phytosterols. In addition, the NADH: flavin oxidoreductase and a water-forming NADH oxidase from Lactobacillus brevis, were successfully overexpressed and heterologously expressed in MNR M3 to improve the intracellular ratio of NAD(+)/NADH. After 96 h of cultivation, the expression of these two enzymes in MNR M3 resulted in the decrease in intracellular NADH level (by 51 and 67%, respectively) and the increase in NAD(+)/NADH ratio (by 113 and 192%, respectively). Phytosterols bioconversion revealed that the conversion ratio of engineered stains was ultimately improved by 58 and 147%, respectively. The highest AD (D) conversion ratio by MNR M3N2 was 94% in the conversion system with soybean oil as reaction media to promote the solubility of phytosterols. CONCLUSIONS: The ratio of NAD(+)/NADH is an important factor for the transformation of phytosterols. Expression of NADH: flavin oxidoreductase and water-forming NADH oxidase in MNR improved AD (D) production. Besides the manipulation of key enzyme activities, which included in phytosterols degradation pathways, maintenance the balance of redox also played an important role in promoting steroid biotransformation. The recombinant MNR strain may be useful in industrial production. BioMed Central 2017-10-30 /pmc/articles/PMC5663084/ /pubmed/29084539 http://dx.doi.org/10.1186/s12934-017-0796-4 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Su, Liqiu
Shen, Yanbing
Zhang, Wenkai
Gao, Tian
Shang, Zhihua
Wang, Min
Cofactor engineering to regulate NAD(+)/NADH ratio with its application to phytosterols biotransformation
title Cofactor engineering to regulate NAD(+)/NADH ratio with its application to phytosterols biotransformation
title_full Cofactor engineering to regulate NAD(+)/NADH ratio with its application to phytosterols biotransformation
title_fullStr Cofactor engineering to regulate NAD(+)/NADH ratio with its application to phytosterols biotransformation
title_full_unstemmed Cofactor engineering to regulate NAD(+)/NADH ratio with its application to phytosterols biotransformation
title_short Cofactor engineering to regulate NAD(+)/NADH ratio with its application to phytosterols biotransformation
title_sort cofactor engineering to regulate nad(+)/nadh ratio with its application to phytosterols biotransformation
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5663084/
https://www.ncbi.nlm.nih.gov/pubmed/29084539
http://dx.doi.org/10.1186/s12934-017-0796-4
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