Loading…

Efficient Biosynthesis of (S)-1-chloro-2-heptanol Catalyzed by a Newly Isolated Fungi Curvularia hominis B-36

(S)-1-chloro-2-heptanol is an enantiopure chemical of great value that can synthesize Treprostinil for treating primary pulmonary hypertension. In this work, a new strain B-36, capable of asymmetric reduction of 1-chloro-2-heptanone to (S)-1-chloro-2-heptanol, was screened and identified as Curvular...

Full description

Saved in:
Bibliographic Details
Published in:Catalysts 2023-01, Vol.13 (1), p.52
Main Authors: Xu, Shenpeng, Lin, Qinzhe, Chen, Wentian, Lin, Ruoyu, Shen, Yikai, Tang, Pinchuan, Yu, Sisi, Du, Wenting, Li, Jun
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c234t-cf274d3bb832208278f9e76330bedd68a1b7692552ebed673da000747a368fe73
cites cdi_FETCH-LOGICAL-c234t-cf274d3bb832208278f9e76330bedd68a1b7692552ebed673da000747a368fe73
container_end_page
container_issue 1
container_start_page 52
container_title Catalysts
container_volume 13
creator Xu, Shenpeng
Lin, Qinzhe
Chen, Wentian
Lin, Ruoyu
Shen, Yikai
Tang, Pinchuan
Yu, Sisi
Du, Wenting
Li, Jun
description (S)-1-chloro-2-heptanol is an enantiopure chemical of great value that can synthesize Treprostinil for treating primary pulmonary hypertension. In this work, a new strain B-36, capable of asymmetric reduction of 1-chloro-2-heptanone to (S)-1-chloro-2-heptanol, was screened and identified as Curvularia hominis B-36 (CCTCC M 2017654) based on the morphological and internally transcribed spacer (ITS) sequence. The reductive capacity of Curvularia hominis B-36 was investigated as a whole-cell biocatalyst in the bioreduction, and the excellent yield (97.2%) and enantiomeric excess (ee) value (99.9%) were achieved under the optimal conditions as follows: 75 mM 1-chloro-2-heptanone, K2HPO4-KH2PO4 (100 mM, pH 6.0), 50 g L−1 resting cells (dry cell weight; DCW), 15% (v/v) isopropanol as co-substrate, 200 rpm, 30 °C, 20 h. The scaled-up biocatalytic process was accomplished at a bioreactor in a 1.5 L working volume, showing superb yield (~97%) and selectivity (99.9%). The product (S)-1-chloro-2-heptanol was purified and characterized by NMR. Curvularia hominis B-36 is a novel catalyst and the asymmetric synthesis route is benign and eco-friendly.
doi_str_mv 10.3390/catal13010052
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_2767188106</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2767188106</sourcerecordid><originalsourceid>FETCH-LOGICAL-c234t-cf274d3bb832208278f9e76330bedd68a1b7692552ebed673da000747a368fe73</originalsourceid><addsrcrecordid>eNpVULFOwzAUtBBIVKUjuyUWGAy2X2I7I61aqFTBAMyRk9jEVRoXOwGFrydVGeCWdzqd7vQOoUtGbwEyelfqTjcMKKM05SdowqkEkkCSnP7h52gW45aOyBgolk7QbmmtK51pOzx3Pg5tV5voIvYWX7_cEEbKuvHBE05qs-906xu8ODQN36bCxYA1fjJfzYDX0Te6G7VV3747vOjDZ9_o4DSu_c61Y-KcgLhAZ1Y30cx-7xS9rZavi0eyeX5YL-43pOSQdKS0XCYVFIUCzqniUtnMSAFAC1NVQmlWSJHxNOVmFISESo8vyURqEMoaCVN0dczdB__Rm9jlW9-HdqzMuRSSKcWoGF3k6CqDjzEYm--D2-kw5Izmh1Hzf6PCD7d4aPM</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2767188106</pqid></control><display><type>article</type><title>Efficient Biosynthesis of (S)-1-chloro-2-heptanol Catalyzed by a Newly Isolated Fungi Curvularia hominis B-36</title><source>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</source><creator>Xu, Shenpeng ; Lin, Qinzhe ; Chen, Wentian ; Lin, Ruoyu ; Shen, Yikai ; Tang, Pinchuan ; Yu, Sisi ; Du, Wenting ; Li, Jun</creator><creatorcontrib>Xu, Shenpeng ; Lin, Qinzhe ; Chen, Wentian ; Lin, Ruoyu ; Shen, Yikai ; Tang, Pinchuan ; Yu, Sisi ; Du, Wenting ; Li, Jun</creatorcontrib><description>(S)-1-chloro-2-heptanol is an enantiopure chemical of great value that can synthesize Treprostinil for treating primary pulmonary hypertension. In this work, a new strain B-36, capable of asymmetric reduction of 1-chloro-2-heptanone to (S)-1-chloro-2-heptanol, was screened and identified as Curvularia hominis B-36 (CCTCC M 2017654) based on the morphological and internally transcribed spacer (ITS) sequence. The reductive capacity of Curvularia hominis B-36 was investigated as a whole-cell biocatalyst in the bioreduction, and the excellent yield (97.2%) and enantiomeric excess (ee) value (99.9%) were achieved under the optimal conditions as follows: 75 mM 1-chloro-2-heptanone, K2HPO4-KH2PO4 (100 mM, pH 6.0), 50 g L−1 resting cells (dry cell weight; DCW), 15% (v/v) isopropanol as co-substrate, 200 rpm, 30 °C, 20 h. The scaled-up biocatalytic process was accomplished at a bioreactor in a 1.5 L working volume, showing superb yield (~97%) and selectivity (99.9%). The product (S)-1-chloro-2-heptanol was purified and characterized by NMR. Curvularia hominis B-36 is a novel catalyst and the asymmetric synthesis route is benign and eco-friendly.</description><identifier>ISSN: 2073-4344</identifier><identifier>EISSN: 2073-4344</identifier><identifier>DOI: 10.3390/catal13010052</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>Alcohol ; Asymmetry ; Biocatalysts ; Bioreactors ; Biosynthesis ; Carbohydrates ; Catalysis ; Catalysts ; Chemical reactions ; Chemical synthesis ; Dry cells ; Efficiency ; Enzymes ; High temperature ; Hypertension ; NMR ; Nuclear magnetic resonance ; Pharmaceuticals ; Potassium phosphates ; Selectivity ; Substrates</subject><ispartof>Catalysts, 2023-01, Vol.13 (1), p.52</ispartof><rights>2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c234t-cf274d3bb832208278f9e76330bedd68a1b7692552ebed673da000747a368fe73</citedby><cites>FETCH-LOGICAL-c234t-cf274d3bb832208278f9e76330bedd68a1b7692552ebed673da000747a368fe73</cites><orcidid>0000-0001-8998-3952</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2767188106/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2767188106?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,25731,27901,27902,36989,44566,74869</link.rule.ids></links><search><creatorcontrib>Xu, Shenpeng</creatorcontrib><creatorcontrib>Lin, Qinzhe</creatorcontrib><creatorcontrib>Chen, Wentian</creatorcontrib><creatorcontrib>Lin, Ruoyu</creatorcontrib><creatorcontrib>Shen, Yikai</creatorcontrib><creatorcontrib>Tang, Pinchuan</creatorcontrib><creatorcontrib>Yu, Sisi</creatorcontrib><creatorcontrib>Du, Wenting</creatorcontrib><creatorcontrib>Li, Jun</creatorcontrib><title>Efficient Biosynthesis of (S)-1-chloro-2-heptanol Catalyzed by a Newly Isolated Fungi Curvularia hominis B-36</title><title>Catalysts</title><description>(S)-1-chloro-2-heptanol is an enantiopure chemical of great value that can synthesize Treprostinil for treating primary pulmonary hypertension. In this work, a new strain B-36, capable of asymmetric reduction of 1-chloro-2-heptanone to (S)-1-chloro-2-heptanol, was screened and identified as Curvularia hominis B-36 (CCTCC M 2017654) based on the morphological and internally transcribed spacer (ITS) sequence. The reductive capacity of Curvularia hominis B-36 was investigated as a whole-cell biocatalyst in the bioreduction, and the excellent yield (97.2%) and enantiomeric excess (ee) value (99.9%) were achieved under the optimal conditions as follows: 75 mM 1-chloro-2-heptanone, K2HPO4-KH2PO4 (100 mM, pH 6.0), 50 g L−1 resting cells (dry cell weight; DCW), 15% (v/v) isopropanol as co-substrate, 200 rpm, 30 °C, 20 h. The scaled-up biocatalytic process was accomplished at a bioreactor in a 1.5 L working volume, showing superb yield (~97%) and selectivity (99.9%). The product (S)-1-chloro-2-heptanol was purified and characterized by NMR. Curvularia hominis B-36 is a novel catalyst and the asymmetric synthesis route is benign and eco-friendly.</description><subject>Alcohol</subject><subject>Asymmetry</subject><subject>Biocatalysts</subject><subject>Bioreactors</subject><subject>Biosynthesis</subject><subject>Carbohydrates</subject><subject>Catalysis</subject><subject>Catalysts</subject><subject>Chemical reactions</subject><subject>Chemical synthesis</subject><subject>Dry cells</subject><subject>Efficiency</subject><subject>Enzymes</subject><subject>High temperature</subject><subject>Hypertension</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Pharmaceuticals</subject><subject>Potassium phosphates</subject><subject>Selectivity</subject><subject>Substrates</subject><issn>2073-4344</issn><issn>2073-4344</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNpVULFOwzAUtBBIVKUjuyUWGAy2X2I7I61aqFTBAMyRk9jEVRoXOwGFrydVGeCWdzqd7vQOoUtGbwEyelfqTjcMKKM05SdowqkEkkCSnP7h52gW45aOyBgolk7QbmmtK51pOzx3Pg5tV5voIvYWX7_cEEbKuvHBE05qs-906xu8ODQN36bCxYA1fjJfzYDX0Te6G7VV3747vOjDZ9_o4DSu_c61Y-KcgLhAZ1Y30cx-7xS9rZavi0eyeX5YL-43pOSQdKS0XCYVFIUCzqniUtnMSAFAC1NVQmlWSJHxNOVmFISESo8vyURqEMoaCVN0dczdB__Rm9jlW9-HdqzMuRSSKcWoGF3k6CqDjzEYm--D2-kw5Izmh1Hzf6PCD7d4aPM</recordid><startdate>20230101</startdate><enddate>20230101</enddate><creator>Xu, Shenpeng</creator><creator>Lin, Qinzhe</creator><creator>Chen, Wentian</creator><creator>Lin, Ruoyu</creator><creator>Shen, Yikai</creator><creator>Tang, Pinchuan</creator><creator>Yu, Sisi</creator><creator>Du, Wenting</creator><creator>Li, Jun</creator><general>MDPI AG</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>HCIFZ</scope><scope>JG9</scope><scope>KB.</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><orcidid>https://orcid.org/0000-0001-8998-3952</orcidid></search><sort><creationdate>20230101</creationdate><title>Efficient Biosynthesis of (S)-1-chloro-2-heptanol Catalyzed by a Newly Isolated Fungi Curvularia hominis B-36</title><author>Xu, Shenpeng ; Lin, Qinzhe ; Chen, Wentian ; Lin, Ruoyu ; Shen, Yikai ; Tang, Pinchuan ; Yu, Sisi ; Du, Wenting ; Li, Jun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c234t-cf274d3bb832208278f9e76330bedd68a1b7692552ebed673da000747a368fe73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Alcohol</topic><topic>Asymmetry</topic><topic>Biocatalysts</topic><topic>Bioreactors</topic><topic>Biosynthesis</topic><topic>Carbohydrates</topic><topic>Catalysis</topic><topic>Catalysts</topic><topic>Chemical reactions</topic><topic>Chemical synthesis</topic><topic>Dry cells</topic><topic>Efficiency</topic><topic>Enzymes</topic><topic>High temperature</topic><topic>Hypertension</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><topic>Pharmaceuticals</topic><topic>Potassium phosphates</topic><topic>Selectivity</topic><topic>Substrates</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Xu, Shenpeng</creatorcontrib><creatorcontrib>Lin, Qinzhe</creatorcontrib><creatorcontrib>Chen, Wentian</creatorcontrib><creatorcontrib>Lin, Ruoyu</creatorcontrib><creatorcontrib>Shen, Yikai</creatorcontrib><creatorcontrib>Tang, Pinchuan</creatorcontrib><creatorcontrib>Yu, Sisi</creatorcontrib><creatorcontrib>Du, Wenting</creatorcontrib><creatorcontrib>Li, Jun</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>Materials Science &amp; Engineering Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central</collection><collection>SciTech Premium Collection</collection><collection>Materials Research Database</collection><collection>ProQuest Materials Science Database</collection><collection>Materials Science Collection</collection><collection>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><jtitle>Catalysts</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xu, Shenpeng</au><au>Lin, Qinzhe</au><au>Chen, Wentian</au><au>Lin, Ruoyu</au><au>Shen, Yikai</au><au>Tang, Pinchuan</au><au>Yu, Sisi</au><au>Du, Wenting</au><au>Li, Jun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Efficient Biosynthesis of (S)-1-chloro-2-heptanol Catalyzed by a Newly Isolated Fungi Curvularia hominis B-36</atitle><jtitle>Catalysts</jtitle><date>2023-01-01</date><risdate>2023</risdate><volume>13</volume><issue>1</issue><spage>52</spage><pages>52-</pages><issn>2073-4344</issn><eissn>2073-4344</eissn><abstract>(S)-1-chloro-2-heptanol is an enantiopure chemical of great value that can synthesize Treprostinil for treating primary pulmonary hypertension. In this work, a new strain B-36, capable of asymmetric reduction of 1-chloro-2-heptanone to (S)-1-chloro-2-heptanol, was screened and identified as Curvularia hominis B-36 (CCTCC M 2017654) based on the morphological and internally transcribed spacer (ITS) sequence. The reductive capacity of Curvularia hominis B-36 was investigated as a whole-cell biocatalyst in the bioreduction, and the excellent yield (97.2%) and enantiomeric excess (ee) value (99.9%) were achieved under the optimal conditions as follows: 75 mM 1-chloro-2-heptanone, K2HPO4-KH2PO4 (100 mM, pH 6.0), 50 g L−1 resting cells (dry cell weight; DCW), 15% (v/v) isopropanol as co-substrate, 200 rpm, 30 °C, 20 h. The scaled-up biocatalytic process was accomplished at a bioreactor in a 1.5 L working volume, showing superb yield (~97%) and selectivity (99.9%). The product (S)-1-chloro-2-heptanol was purified and characterized by NMR. Curvularia hominis B-36 is a novel catalyst and the asymmetric synthesis route is benign and eco-friendly.</abstract><cop>Basel</cop><pub>MDPI AG</pub><doi>10.3390/catal13010052</doi><orcidid>https://orcid.org/0000-0001-8998-3952</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 2073-4344
ispartof Catalysts, 2023-01, Vol.13 (1), p.52
issn 2073-4344
2073-4344
language eng
recordid cdi_proquest_journals_2767188106
source Publicly Available Content Database (Proquest) (PQ_SDU_P3)
subjects Alcohol
Asymmetry
Biocatalysts
Bioreactors
Biosynthesis
Carbohydrates
Catalysis
Catalysts
Chemical reactions
Chemical synthesis
Dry cells
Efficiency
Enzymes
High temperature
Hypertension
NMR
Nuclear magnetic resonance
Pharmaceuticals
Potassium phosphates
Selectivity
Substrates
title Efficient Biosynthesis of (S)-1-chloro-2-heptanol Catalyzed by a Newly Isolated Fungi Curvularia hominis B-36
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-07T16%3A13%3A54IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Efficient%20Biosynthesis%20of%20(S)-1-chloro-2-heptanol%20Catalyzed%20by%20a%20Newly%20Isolated%20Fungi%20Curvularia%20hominis%20B-36&rft.jtitle=Catalysts&rft.au=Xu,%20Shenpeng&rft.date=2023-01-01&rft.volume=13&rft.issue=1&rft.spage=52&rft.pages=52-&rft.issn=2073-4344&rft.eissn=2073-4344&rft_id=info:doi/10.3390/catal13010052&rft_dat=%3Cproquest_cross%3E2767188106%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c234t-cf274d3bb832208278f9e76330bedd68a1b7692552ebed673da000747a368fe73%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2767188106&rft_id=info:pmid/&rfr_iscdi=true