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dc.contributor.authorYeh, Hsu-Huaen_US
dc.contributor.authorChang, Shu-Linen_US
dc.contributor.authorChiang, Yi-Mingen_US
dc.contributor.authorBruno, Kenneth S.en_US
dc.contributor.authorOakley, Berl R.en_US
dc.contributor.authorWu, Tung-Kungen_US
dc.contributor.authorWang, Clay C. C.en_US
dc.date.accessioned2014-12-08T15:29:54Z-
dc.date.available2014-12-08T15:29:54Z-
dc.date.issued2013-02-15en_US
dc.identifier.issn1523-7060en_US
dc.identifier.urihttp://dx.doi.org/10.1021/ol303328ten_US
dc.identifier.urihttp://hdl.handle.net/11536/21435-
dc.description.abstractWe reannotated the A. niger NR-PKS gene, e_gw1_19.204, and its downstream R domain gene, est_GWPlus_C_190476, as a single gene which we named dtbA. Heterologous expression of dtbA In A. nidulans demonstrated that DtbA protein produces two polyketides, 2,4-dihydroxy-3,5,6-trimethylbenzaldehyde (1) and 6-ethyl-2,4-dihydroxy-3,5-dimethylbenzaldehyde (2). Generation of DtbA Delta R+TE chimeric PKSs by swapping the DtbA R domain with the AusA (austinol biosynthesis) or ANID_06448 TE domain enabled the production of two metabolites with carboxylic acids replacing the corresponding aldehydes.en_US
dc.language.isoen_USen_US
dc.titleEngineering Fungal Nonreducing Polyketide Synthase by Heterologous Expression and Domain Swappingen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/ol303328ten_US
dc.identifier.journalORGANIC LETTERSen_US
dc.citation.volume15en_US
dc.citation.issue4en_US
dc.citation.spage756en_US
dc.citation.epage759en_US
dc.contributor.department生物科技學系zh_TW
dc.contributor.departmentDepartment of Biological Science and Technologyen_US
dc.identifier.wosnumberWOS:000315254500010-
dc.citation.woscount8-
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