Microbiological transformations 52.: Biocatalysed Baeyer–Villiger oxidation of 1-indanone derivatives
The microbiological Baeyer–Villiger oxidation of various substituted 1-indanones is described. Three bacterial strains have been explored: an E. coli TOP10 [pQR 239] constructed to overexpress the cyclohexanone monoxygenase (CHMO) of Acinetobacter calcoaceticus NCIMB 9871, an E. coli TOP10 [hapE] st...
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| Veröffentlicht in: | Journal of molecular catalysis. B, Enzymatic Enzymatic, 2003-02, Vol.21 (4), p.231-238 |
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| container_title | Journal of molecular catalysis. B, Enzymatic |
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| creator | Gutiérrez, Marı́a C Alphand, Véronique Furstoss, Roland |
| description | The microbiological Baeyer–Villiger oxidation of various substituted 1-indanones is described. Three bacterial strains have been explored: an
E. coli TOP10 [pQR 239] constructed to overexpress the cyclohexanone monoxygenase (CHMO) of
Acinetobacter calcoaceticus NCIMB 9871, an
E. coli TOP10 [hapE] strain recently constructed to overexpress 4-hydroxyacetophenone monoxygenase (HAPMO) of
Pseudomonas fluorescens ACB and the wild type
Pseudomonas sp. NCIMB 9872 strain known to metabolise cyclopentanone. This last strain oxidised some of the proposed substrates, leading to the corresponding lactones with good to excellent yields depending on the aromatic ring substituents. |
| doi_str_mv | 10.1016/S1381-1177(02)00227-8 |
| format | Article |
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E. coli TOP10 [pQR 239] constructed to overexpress the cyclohexanone monoxygenase (CHMO) of
Acinetobacter calcoaceticus NCIMB 9871, an
E. coli TOP10 [hapE] strain recently constructed to overexpress 4-hydroxyacetophenone monoxygenase (HAPMO) of
Pseudomonas fluorescens ACB and the wild type
Pseudomonas sp. NCIMB 9872 strain known to metabolise cyclopentanone. This last strain oxidised some of the proposed substrates, leading to the corresponding lactones with good to excellent yields depending on the aromatic ring substituents.</description><identifier>ISSN: 1381-1177</identifier><identifier>EISSN: 1873-3158</identifier><identifier>DOI: 10.1016/S1381-1177(02)00227-8</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>1-Indanones ; Baeyer–Villiger oxidation ; Bioconversions. Hemisynthesis ; Biological and medical sciences ; Biotechnology ; Fundamental and applied biological sciences. Psychology ; Methods. Procedures. Technologies ; Overexpressed Baeyer–Villigerase ; Recombinant microorganisms ; Whole cell biotransformation</subject><ispartof>Journal of molecular catalysis. B, Enzymatic, 2003-02, Vol.21 (4), p.231-238</ispartof><rights>2002 Elsevier Science B.V.</rights><rights>2003 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1381117702002278$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65534</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14441999$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Gutiérrez, Marı́a C</creatorcontrib><creatorcontrib>Alphand, Véronique</creatorcontrib><creatorcontrib>Furstoss, Roland</creatorcontrib><title>Microbiological transformations 52.: Biocatalysed Baeyer–Villiger oxidation of 1-indanone derivatives</title><title>Journal of molecular catalysis. B, Enzymatic</title><description>The microbiological Baeyer–Villiger oxidation of various substituted 1-indanones is described. Three bacterial strains have been explored: an
E. coli TOP10 [pQR 239] constructed to overexpress the cyclohexanone monoxygenase (CHMO) of
Acinetobacter calcoaceticus NCIMB 9871, an
E. coli TOP10 [hapE] strain recently constructed to overexpress 4-hydroxyacetophenone monoxygenase (HAPMO) of
Pseudomonas fluorescens ACB and the wild type
Pseudomonas sp. NCIMB 9872 strain known to metabolise cyclopentanone. This last strain oxidised some of the proposed substrates, leading to the corresponding lactones with good to excellent yields depending on the aromatic ring substituents.</description><subject>1-Indanones</subject><subject>Baeyer–Villiger oxidation</subject><subject>Bioconversions. Hemisynthesis</subject><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Methods. Procedures. Technologies</subject><subject>Overexpressed Baeyer–Villigerase</subject><subject>Recombinant microorganisms</subject><subject>Whole cell biotransformation</subject><issn>1381-1177</issn><issn>1873-3158</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><recordid>eNo1kMtKAzEUhoMoWKuPIGQj6GJqTtK0GTdiizeouPCyDZnkpESmk5IMxe58B9_QJ3Ha6uocOB8_5_8IOQU2AAajyxcQCgqA8fic8QvGOB8Xao_0QI1FIUCq_W7_Rw7JUc4frKMAVI_Mn4JNsQqxjvNgTU3bZJrsY1qYNsQmU8kHV3QSojWtqdcZHZ0YXGP6-fp-D3Ud5pho_Axui9PoKRShcaaJDVKHKay6wwrzMTnwps548jf75O3u9nX6UMye7x-nN7MCuSjbwjuGklvnjeMCvSvRcKYsSmmqSgjuvGWorARljTSlHTlfeu8RqpGSpXeiT852uUuTuzq-a2ND1ssUFiatNQyHQyjLsuOudxx2z6wCJp1twMaiCwltq10MGpje-NVbv3ojTzOut361Er854nMV</recordid><startdate>20030217</startdate><enddate>20030217</enddate><creator>Gutiérrez, Marı́a C</creator><creator>Alphand, Véronique</creator><creator>Furstoss, Roland</creator><general>Elsevier B.V</general><general>Elsevier Science</general><scope>IQODW</scope></search><sort><creationdate>20030217</creationdate><title>Microbiological transformations 52.: Biocatalysed Baeyer–Villiger oxidation of 1-indanone derivatives</title><author>Gutiérrez, Marı́a C ; Alphand, Véronique ; Furstoss, Roland</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-e239t-fd0e52cdfad23efd9ea208ce55abb332dfc0e8c518ca5a9c6df9fffe1b6859fd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>1-Indanones</topic><topic>Baeyer–Villiger oxidation</topic><topic>Bioconversions. Hemisynthesis</topic><topic>Biological and medical sciences</topic><topic>Biotechnology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Methods. Procedures. Technologies</topic><topic>Overexpressed Baeyer–Villigerase</topic><topic>Recombinant microorganisms</topic><topic>Whole cell biotransformation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gutiérrez, Marı́a C</creatorcontrib><creatorcontrib>Alphand, Véronique</creatorcontrib><creatorcontrib>Furstoss, Roland</creatorcontrib><collection>Pascal-Francis</collection><jtitle>Journal of molecular catalysis. B, Enzymatic</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gutiérrez, Marı́a C</au><au>Alphand, Véronique</au><au>Furstoss, Roland</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Microbiological transformations 52.: Biocatalysed Baeyer–Villiger oxidation of 1-indanone derivatives</atitle><jtitle>Journal of molecular catalysis. B, Enzymatic</jtitle><date>2003-02-17</date><risdate>2003</risdate><volume>21</volume><issue>4</issue><spage>231</spage><epage>238</epage><pages>231-238</pages><issn>1381-1177</issn><eissn>1873-3158</eissn><abstract>The microbiological Baeyer–Villiger oxidation of various substituted 1-indanones is described. Three bacterial strains have been explored: an
E. coli TOP10 [pQR 239] constructed to overexpress the cyclohexanone monoxygenase (CHMO) of
Acinetobacter calcoaceticus NCIMB 9871, an
E. coli TOP10 [hapE] strain recently constructed to overexpress 4-hydroxyacetophenone monoxygenase (HAPMO) of
Pseudomonas fluorescens ACB and the wild type
Pseudomonas sp. NCIMB 9872 strain known to metabolise cyclopentanone. This last strain oxidised some of the proposed substrates, leading to the corresponding lactones with good to excellent yields depending on the aromatic ring substituents.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><doi>10.1016/S1381-1177(02)00227-8</doi><tpages>8</tpages></addata></record> |
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| ispartof | Journal of molecular catalysis. B, Enzymatic, 2003-02, Vol.21 (4), p.231-238 |
| issn | 1381-1177 1873-3158 |
| language | eng |
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| source | Elsevier ScienceDirect Journals Complete |
| subjects | 1-Indanones Baeyer–Villiger oxidation Bioconversions. Hemisynthesis Biological and medical sciences Biotechnology Fundamental and applied biological sciences. Psychology Methods. Procedures. Technologies Overexpressed Baeyer–Villigerase Recombinant microorganisms Whole cell biotransformation |
| title | Microbiological transformations 52.: Biocatalysed Baeyer–Villiger oxidation of 1-indanone derivatives |
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