Enantioselective hydrolysis of cyclopentaneacetic acid esters related to methyl jasmonate
The hydrolysis of methyl jasmonate with Aspergillus niger and A. carbonarius is shown to be very dependent upon the particular structure of the substrate. Some variation of the side chain at C-2 is tolerated, whereas the 3-keto group and the methyl ester moieties are particularly important. Porcine...
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| Veröffentlicht in: | Enzyme and microbial technology 1993, Vol.15 (10), p.818-820 |
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| container_title | Enzyme and microbial technology |
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| creator | Kerry, S. Dart, R.K. Marples, B.A. |
| description | The hydrolysis of methyl jasmonate with
Aspergillus niger and
A. carbonarius is shown to be very dependent upon the particular structure of the substrate. Some variation of the side chain at C-2 is tolerated, whereas the 3-keto group and the methyl ester moieties are particularly important. Porcine pancreatic lipase,
Candida lipase, and
Rhizopus lipase are unreactive towards butyl jasmonate. |
| doi_str_mv | 10.1016/0141-0229(93)90092-G |
| format | Article |
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Aspergillus niger and
A. carbonarius is shown to be very dependent upon the particular structure of the substrate. Some variation of the side chain at C-2 is tolerated, whereas the 3-keto group and the methyl ester moieties are particularly important. Porcine pancreatic lipase,
Candida lipase, and
Rhizopus lipase are unreactive towards butyl jasmonate.</description><identifier>ISSN: 0141-0229</identifier><identifier>EISSN: 1879-0909</identifier><identifier>DOI: 10.1016/0141-0229(93)90092-G</identifier><identifier>CODEN: EMTED2</identifier><language>eng</language><publisher>Amsterdam: Elsevier Inc</publisher><subject>Aspergillus carbonarius ; Aspergillus niger ; Bioconversions. Hemisynthesis ; Biological and medical sciences ; Biotechnology ; cyclopentaneacetic acid esters ; Enantioselective hydrolysis ; Fundamental and applied biological sciences. Psychology ; Methods. Procedures. Technologies ; methyl jasmonate</subject><ispartof>Enzyme and microbial technology, 1993, Vol.15 (10), p.818-820</ispartof><rights>1993</rights><rights>1994 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c364t-1373e1a49e105d652460e0e81e99dcb94ff6157eb69283ba9f89d2457b6eb2c53</citedby><cites>FETCH-LOGICAL-c364t-1373e1a49e105d652460e0e81e99dcb94ff6157eb69283ba9f89d2457b6eb2c53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/0141-0229(93)90092-G$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3549,4023,27922,27923,27924,45994</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3834692$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Kerry, S.</creatorcontrib><creatorcontrib>Dart, R.K.</creatorcontrib><creatorcontrib>Marples, B.A.</creatorcontrib><title>Enantioselective hydrolysis of cyclopentaneacetic acid esters related to methyl jasmonate</title><title>Enzyme and microbial technology</title><description>The hydrolysis of methyl jasmonate with
Aspergillus niger and
A. carbonarius is shown to be very dependent upon the particular structure of the substrate. Some variation of the side chain at C-2 is tolerated, whereas the 3-keto group and the methyl ester moieties are particularly important. Porcine pancreatic lipase,
Candida lipase, and
Rhizopus lipase are unreactive towards butyl jasmonate.</description><subject>Aspergillus carbonarius</subject><subject>Aspergillus niger</subject><subject>Bioconversions. Hemisynthesis</subject><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>cyclopentaneacetic acid esters</subject><subject>Enantioselective hydrolysis</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Methods. Procedures. Technologies</subject><subject>methyl jasmonate</subject><issn>0141-0229</issn><issn>1879-0909</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1993</creationdate><recordtype>article</recordtype><recordid>eNp9kE1LxDAQhoMouH78Aw85iOihmjRp2lwEkXUVBC968BTSdMpmSZs1yQr992bdxaOngeGZmXcehC4ouaWEijtCOS1IWcpryW4kIbIsFgdoRptaFkQSeYhmf8gxOolxRUhucDJDn_NRj8n6CA5Mst-Al1MXvJuijdj32EzG-TWMSY-gDSRrsDa2wxAThIgDOJ2gw8njAdJycnil4-DH3DxDR712Ec739RR9PM3fH5-L17fFy-PDa2GY4KmgrGZANZdASdWJquSCAIGGgpSdaSXve0GrGlohy4a1WvaN7Epe1a2AtjQVO0VXu73r4L82OZcabDTgXE7sN1FRIahoappBvgNN8DEG6NU62EGHSVGith7VVpLaSlKSqV-PapHHLvf7dTTa9UGPxsa_WdYwnqNl7H6HQf7120JQ0VgYDXQ2ZLOq8_b_Oz9FA4fk</recordid><startdate>1993</startdate><enddate>1993</enddate><creator>Kerry, S.</creator><creator>Dart, R.K.</creator><creator>Marples, B.A.</creator><general>Elsevier Inc</general><general>Elsevier Science</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>1993</creationdate><title>Enantioselective hydrolysis of cyclopentaneacetic acid esters related to methyl jasmonate</title><author>Kerry, S. ; Dart, R.K. ; Marples, B.A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c364t-1373e1a49e105d652460e0e81e99dcb94ff6157eb69283ba9f89d2457b6eb2c53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1993</creationdate><topic>Aspergillus carbonarius</topic><topic>Aspergillus niger</topic><topic>Bioconversions. Hemisynthesis</topic><topic>Biological and medical sciences</topic><topic>Biotechnology</topic><topic>cyclopentaneacetic acid esters</topic><topic>Enantioselective hydrolysis</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Methods. Procedures. Technologies</topic><topic>methyl jasmonate</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kerry, S.</creatorcontrib><creatorcontrib>Dart, R.K.</creatorcontrib><creatorcontrib>Marples, B.A.</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Enzyme and microbial technology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kerry, S.</au><au>Dart, R.K.</au><au>Marples, B.A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Enantioselective hydrolysis of cyclopentaneacetic acid esters related to methyl jasmonate</atitle><jtitle>Enzyme and microbial technology</jtitle><date>1993</date><risdate>1993</risdate><volume>15</volume><issue>10</issue><spage>818</spage><epage>820</epage><pages>818-820</pages><issn>0141-0229</issn><eissn>1879-0909</eissn><coden>EMTED2</coden><abstract>The hydrolysis of methyl jasmonate with
Aspergillus niger and
A. carbonarius is shown to be very dependent upon the particular structure of the substrate. Some variation of the side chain at C-2 is tolerated, whereas the 3-keto group and the methyl ester moieties are particularly important. Porcine pancreatic lipase,
Candida lipase, and
Rhizopus lipase are unreactive towards butyl jasmonate.</abstract><cop>Amsterdam</cop><pub>Elsevier Inc</pub><doi>10.1016/0141-0229(93)90092-G</doi><tpages>3</tpages></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 0141-0229 |
| ispartof | Enzyme and microbial technology, 1993, Vol.15 (10), p.818-820 |
| issn | 0141-0229 1879-0909 |
| language | eng |
| recordid | cdi_proquest_miscellaneous_16616871 |
| source | Elsevier ScienceDirect Journals Complete - AutoHoldings |
| subjects | Aspergillus carbonarius Aspergillus niger Bioconversions. Hemisynthesis Biological and medical sciences Biotechnology cyclopentaneacetic acid esters Enantioselective hydrolysis Fundamental and applied biological sciences. Psychology Methods. Procedures. Technologies methyl jasmonate |
| title | Enantioselective hydrolysis of cyclopentaneacetic acid esters related to methyl jasmonate |
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