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Mutation of isoleucine 705 of the oxidosqualene-lanosterol cyclase from Saccharomyces cerevisiae affects lanosterol's C/D-ring cyclization and 17 alpha/beta-exocyclic side chain stereochemistry

dc.citation.epage1097en_US
dc.citation.issue4en_US
dc.citation.spage1092en_US
dc.citation.volume9en_US
dc.citation.woscount6
dc.contributor.authorWu, Tung-Kungen_US
dc.contributor.authorChang, Yi-Chunen_US
dc.contributor.authorLiu, Yuan-Tingen_US
dc.contributor.authorChang, Cheng-Hsiangen_US
dc.contributor.authorWen, Hao-Yuen_US
dc.contributor.authorLi, Wen-Hsuanen_US
dc.contributor.authorShie, Wen-Shiangen_US
dc.contributor.department生物科技學系zh_TW
dc.contributor.departmentDepartment of Biological Science and Technologyen_US
dc.date.accessioned2014-12-08T15:38:03Z
dc.date.available2014-12-08T15:38:03Z
dc.date.issued2011en_US
dc.description.abstractSite-saturated substitution in Saccharomyces cerevisiae oxidosqualene-lanosterol cyclase at Ile705 position produced three chair-boat-chair (C-B-C) truncated tricyclic compounds, two 17 alpha-exocyclic protosteryl intermediates, two protosteryl C-17 truncated rearranged intermediates and the normal biosynthetic product, lanosterol. These results indicated the importance of the Ile705 residue in affecting lanosterol's C/D ring stabilization including 6-6-5 tricyclic and protosteryl C-17 cations and 17 alpha/beta-exocyclic side chain stereochemistry.en_US
dc.identifier.doi10.1039/c0ob00582gen_US
dc.identifier.issn1477-0520en_US
dc.identifier.journalORGANIC & BIOMOLECULAR CHEMISTRYen_US
dc.identifier.urihttp://dx.doi.org/10.1039/c0ob00582gen_US
dc.identifier.urihttps://ir.lib.nycu.edu.tw/handle/11536/26104
dc.identifier.wosnumberWOS:000286895900021
dc.language.isoen_USen_US
dc.titleMutation of isoleucine 705 of the oxidosqualene-lanosterol cyclase from Saccharomyces cerevisiae affects lanosterol's C/D-ring cyclization and 17 alpha/beta-exocyclic side chain stereochemistryen_US
dc.typeArticleen_US

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