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Molecular cloning and functional characterization of three terpene synthases from unripe fruit of black pepper (Piper nigrum).
Jin, Zhehao; Kwon, Moonhyuk; Lee, Ah-Reum; Ro, Dae-Kyun; Wungsintaweekul, Juraithip; Kim, Soo-Un.
Afiliación
  • Jin Z; Department of Agricultural Biotechnology and Research Institute for Agricultural Sciences, Seoul National University, Seoul 08826, Republic of Korea.
  • Kwon M; Department of Agricultural Biotechnology and Research Institute for Agricultural Sciences, Seoul National University, Seoul 08826, Republic of Korea; Department of Biological Sciences, University of Calgary, Calgary, Canada.
  • Lee AR; Department of Agricultural Biotechnology and Research Institute for Agricultural Sciences, Seoul National University, Seoul 08826, Republic of Korea.
  • Ro DK; Department of Biological Sciences, University of Calgary, Calgary, Canada.
  • Wungsintaweekul J; Department of Pharmacognosy and Pharmaceutical Botany, Faculty of Pharmaceutical Sciences, Prince of Songkla University, Hat Yai, Songkla, Thailand.
  • Kim SU; Department of Agricultural Biotechnology and Research Institute for Agricultural Sciences, Seoul National University, Seoul 08826, Republic of Korea; College of Horticulture and Gardening, Yangtze University, Jingzhou, Hubei, China. Electronic address: soounkim@snu.ac.kr.
Arch Biochem Biophys ; 638: 35-40, 2018 01 15.
Article en En | MEDLINE | ID: mdl-29248443
ABSTRACT
To identify terpene synthases (TPS) responsible for the biosynthesis of the sesquiterpenes that contribute to the characteristic flavors of black pepper (Piper nigrum), unripe peppercorn was subjected to the Illumina transcriptome sequencing. The BLAST analysis using amorpha-4,11-diene synthase as a query identified 19 sesquiterpene synthases (sesqui-TPSs), of which three full-length cDNAs (PnTPS1 through 3) were cloned. These sesqui-TPS cDNAs were expressed in E. coli to produce recombinant enzymes for in vitro assays, and also expressed in the engineered yeast strain to assess their catalytic activities in vivo. PnTPS1 produced ß-caryophyllene as a main product and humulene as a minor compound, and thus was named caryophyllene synthase (PnCPS). Likewise, PnTPS2 and PnTPS3 were, respectively, named cadinol/cadinene synthase (PnCO/CDS) and germacrene D synthase (PnGDS). PnGDS expression in yeast yielded ß-cadinene and α-copaene, the rearrangement products of germacrene D. Their kcat/Km values (20-37.7 s-1 mM-1) were comparable to those of other sesqui-TPSs. Among three PnTPSs, the transcript level of PnCPS was the highest, correlating with the predominant ß-caryophyllene biosynthesis in the peppercorn. The products and rearranged products of three PnTPSs could account for about a half of the sesquiterpenes in number found in unripe peppercorn.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteínas de Plantas / Clonación Molecular / Transferasas Alquil y Aril / Piper nigrum / Frutas Tipo de estudio: Prognostic_studies Idioma: En Revista: Arch Biochem Biophys Año: 2018 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Proteínas de Plantas / Clonación Molecular / Transferasas Alquil y Aril / Piper nigrum / Frutas Tipo de estudio: Prognostic_studies Idioma: En Revista: Arch Biochem Biophys Año: 2018 Tipo del documento: Article