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dc.contributor.authorNakanishi, Yuji
dc.contributor.authorWatanabe, Hidemi
dc.contributor.authorWashizu, Kinya
dc.contributor.authorNarahashi, Yoshiko
dc.contributor.authorKurono, Yoshiaki
dc.date.accessioned2024-03-27T08:30:59Z
dc.date.available2024-03-27T08:30:59Z
dc.date.issued1991
dc.date.submitted2024-03-27
dc.identifier.citationLipases : structure, mechanism and genetic engineering, 263 - 266en_US
dc.identifier.isbn3527283323
dc.identifier.isbn156081165X
dc.identifier.issn0930-4320
dc.identifier.urihttp://hdl.handle.net/10033/623724
dc.description.abstractThelipase gene from Pseudomonas sp. M-12-33 was cloned. The cloned DNA was 2.9 Kb in length, which was essential for production of the lipase and contained two open reading frames, lipA and lipX. The lipA gene was supposed to comprise 1092 nucleotides and give a preproprotein of 364 aminoacids which was then processed to a mature lipase protein of 320 amino acids. On the other hand, the lipX gene was assumedto code a protein of 344 amino acids concerned with someregulation of the enzyme production.en_US
dc.language.isoenen_US
dc.publisherGBF Gesellschaft für Biotechnologische Forschung mbH, Braunschweigen_US
dc.relation.ispartofseriesGBF monographs ; Volume 16en_US
dc.rightsAttribution-NonCommercial-ShareAlike 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/*
dc.titleCLONING, SEQUENCING AND REGULATION OF THE LIPASE GENE FROM PSEUDOMONASSP. M-12-33en_US
dc.typeBook chapteren_US
dc.typeconference paperen_US
dc.contributor.departmentAmano Pharmaceutical Co., Ltd., Kunotsubo, Nishiharu-cho, Nishikasugai-gun, Aichi, Japan; The Institute of Physical and Chemical Research, Hirosawa, Wako-shi, Saitama, Japanen_US
dc.identifier.journalLipases : structure, mechanism and genetic engineering, 1991en_US
refterms.dateFOA2024-03-27T08:31:01Z


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