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Engineering a short-chain dehydrogenase/reductase for the stereoselective production of (2S,3R,4S)-4-hydroxyisoleucine with three asymmetric centers

Fenugreek is a dietary supplement for anti-aging and human health. (2S,3R,4S)-4-hydroxyisoleucine (4-HIL), which is extracted from fenugreek seeds, is expected to be a promising orally active drug for diabetes and diabetic nephropathy because of its insulinotropic effect. Although several chemical s...

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Autores principales: Shi, Xuan, Miyakawa, Takuya, Nakamura, Akira, Hou, Feng, Hibi, Makoto, Ogawa, Jun, Kwon, Yeondae, Tanokura, Masaru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5651801/
https://www.ncbi.nlm.nih.gov/pubmed/29057974
http://dx.doi.org/10.1038/s41598-017-13978-w
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author Shi, Xuan
Miyakawa, Takuya
Nakamura, Akira
Hou, Feng
Hibi, Makoto
Ogawa, Jun
Kwon, Yeondae
Tanokura, Masaru
author_facet Shi, Xuan
Miyakawa, Takuya
Nakamura, Akira
Hou, Feng
Hibi, Makoto
Ogawa, Jun
Kwon, Yeondae
Tanokura, Masaru
author_sort Shi, Xuan
collection PubMed
description Fenugreek is a dietary supplement for anti-aging and human health. (2S,3R,4S)-4-hydroxyisoleucine (4-HIL), which is extracted from fenugreek seeds, is expected to be a promising orally active drug for diabetes and diabetic nephropathy because of its insulinotropic effect. Although several chemical synthesis methods of 4-HIL have been proposed, these methods require multistep reactions to control the stereochemistry of 4-HIL. In this study, we modified the key enzyme 4-HIL dehydrogenase (HILDH) to overcome the biggest limitation in commercial-scale production of 4-HIL. As a result, an effective one-step carbonyl reduction to produce (2S,3R,4S)-4-HIL was successfully accomplished with strict stereoselectivity (>99% de). Mass production of (2S,3R,4S)-4-HIL by our synthetic method could have a significant contribution to the prevention of diabetes, dyslipidemia, and Alzheimer’s disease. (120 words/200 words)
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spelling pubmed-56518012017-10-26 Engineering a short-chain dehydrogenase/reductase for the stereoselective production of (2S,3R,4S)-4-hydroxyisoleucine with three asymmetric centers Shi, Xuan Miyakawa, Takuya Nakamura, Akira Hou, Feng Hibi, Makoto Ogawa, Jun Kwon, Yeondae Tanokura, Masaru Sci Rep Article Fenugreek is a dietary supplement for anti-aging and human health. (2S,3R,4S)-4-hydroxyisoleucine (4-HIL), which is extracted from fenugreek seeds, is expected to be a promising orally active drug for diabetes and diabetic nephropathy because of its insulinotropic effect. Although several chemical synthesis methods of 4-HIL have been proposed, these methods require multistep reactions to control the stereochemistry of 4-HIL. In this study, we modified the key enzyme 4-HIL dehydrogenase (HILDH) to overcome the biggest limitation in commercial-scale production of 4-HIL. As a result, an effective one-step carbonyl reduction to produce (2S,3R,4S)-4-HIL was successfully accomplished with strict stereoselectivity (>99% de). Mass production of (2S,3R,4S)-4-HIL by our synthetic method could have a significant contribution to the prevention of diabetes, dyslipidemia, and Alzheimer’s disease. (120 words/200 words) Nature Publishing Group UK 2017-10-20 /pmc/articles/PMC5651801/ /pubmed/29057974 http://dx.doi.org/10.1038/s41598-017-13978-w Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Shi, Xuan
Miyakawa, Takuya
Nakamura, Akira
Hou, Feng
Hibi, Makoto
Ogawa, Jun
Kwon, Yeondae
Tanokura, Masaru
Engineering a short-chain dehydrogenase/reductase for the stereoselective production of (2S,3R,4S)-4-hydroxyisoleucine with three asymmetric centers
title Engineering a short-chain dehydrogenase/reductase for the stereoselective production of (2S,3R,4S)-4-hydroxyisoleucine with three asymmetric centers
title_full Engineering a short-chain dehydrogenase/reductase for the stereoselective production of (2S,3R,4S)-4-hydroxyisoleucine with three asymmetric centers
title_fullStr Engineering a short-chain dehydrogenase/reductase for the stereoselective production of (2S,3R,4S)-4-hydroxyisoleucine with three asymmetric centers
title_full_unstemmed Engineering a short-chain dehydrogenase/reductase for the stereoselective production of (2S,3R,4S)-4-hydroxyisoleucine with three asymmetric centers
title_short Engineering a short-chain dehydrogenase/reductase for the stereoselective production of (2S,3R,4S)-4-hydroxyisoleucine with three asymmetric centers
title_sort engineering a short-chain dehydrogenase/reductase for the stereoselective production of (2s,3r,4s)-4-hydroxyisoleucine with three asymmetric centers
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5651801/
https://www.ncbi.nlm.nih.gov/pubmed/29057974
http://dx.doi.org/10.1038/s41598-017-13978-w
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