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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...
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Published in: | Catalysts 2023-01, Vol.13 (1), p.52 |
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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. |
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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 & 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> |
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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 |
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