Добірка наукової літератури з теми "Sesquiterpene synthases"
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Статті в журналах з теми "Sesquiterpene synthases"
Yan, Xiaoguang, Yukun Li, Weiguo Li, Dongmei Liang, Shengxin Nie, Ruiqi Chen, Jianjun Qiao, Mingzhang Wen, and Qinggele Caiyin. "Transcriptome Analysis and Identification of Sesquiterpene Synthases in Liverwort Jungermannia exsertifolia." Bioengineering 10, no. 5 (May 9, 2023): 569. http://dx.doi.org/10.3390/bioengineering10050569.
Повний текст джерелаBeran, Franziska, Peter Rahfeld, Katrin Luck, Raimund Nagel, Heiko Vogel, Natalie Wielsch, Sandra Irmisch, et al. "Novel family of terpene synthases evolved from trans-isoprenyl diphosphate synthases in a flea beetle." Proceedings of the National Academy of Sciences 113, no. 11 (March 2, 2016): 2922–27. http://dx.doi.org/10.1073/pnas.1523468113.
Повний текст джерелаCong, Zhanren, Qiang Yin, Kunhong Tian, Njeru Joe Mukoma, Liming Ouyang, Tom Hsiang, Lixin Zhang, Lan Jiang, and Xueting Liu. "Genome Mining of Fungal Unique Trichodiene Synthase-like Sesquiterpene Synthases." Journal of Fungi 10, no. 5 (May 13, 2024): 350. http://dx.doi.org/10.3390/jof10050350.
Повний текст джерелаSilva, Waldeyr M. C. da, Jakob L. Andersen, Maristela T. Holanda, Maria Emília M. T. Walter, Marcelo M. Brigido, Peter F. Stadler, and Christoph Flamm. "Exploring Plant Sesquiterpene Diversity by Generating Chemical Networks." Processes 7, no. 4 (April 25, 2019): 240. http://dx.doi.org/10.3390/pr7040240.
Повний текст джерелаKer, De-Sheng, Sze Lei Pang, Noor Farhan Othman, Sekar Kumaran, Ee Fun Tan, Thiba Krishnan, Kok Gan Chan, Roohaida Othman, Maizom Hassan та Chyan Leong Ng. "Purification and biochemical characterization of recombinant Persicaria minor β-sesquiphellandrene synthase". PeerJ 5 (28 лютого 2017): e2961. http://dx.doi.org/10.7717/peerj.2961.
Повний текст джерелаEe, Su-Fang, Zeti-Azura Mohamed-Hussein, Roohaida Othman, Noor Azmi Shaharuddin, Ismanizan Ismail, and Zamri Zainal. "Functional Characterization of Sesquiterpene Synthase fromPolygonum minus." Scientific World Journal 2014 (2014): 1–11. http://dx.doi.org/10.1155/2014/840592.
Повний текст джерелаYamada, Yuuki, Tomohisa Kuzuyama, Mamoru Komatsu, Kazuo Shin-ya, Satoshi Omura, David E. Cane, and Haruo Ikeda. "Terpene synthases are widely distributed in bacteria." Proceedings of the National Academy of Sciences 112, no. 3 (December 22, 2014): 857–62. http://dx.doi.org/10.1073/pnas.1422108112.
Повний текст джерелаSun, Xiang, You-Sheng Cai, Yujie Yuan, Guangkai Bian, Ziling Ye, Zixin Deng, and Tiangang Liu. "Genome mining in Trichoderma viride J1-030: discovery and identification of novel sesquiterpene synthase and its products." Beilstein Journal of Organic Chemistry 15 (August 28, 2019): 2052–58. http://dx.doi.org/10.3762/bjoc.15.202.
Повний текст джерелаLiang, Dongmei, Weiguo Li, Xiaoguang Yan, Qinggele Caiyin, Guangrong Zhao, and Jianjun Qiao. "Molecular and Functional Evolution of the Spermatophyte Sesquiterpene Synthases." International Journal of Molecular Sciences 22, no. 12 (June 14, 2021): 6348. http://dx.doi.org/10.3390/ijms22126348.
Повний текст джерелаManczak, Tom, and Henrik Toft Simonsen. "Insight into Biochemical Characterization of Plant Sesquiterpene Synthases." Analytical Chemistry Insights 11s1 (January 2016): ACI.S40292. http://dx.doi.org/10.4137/aci.s40292.
Повний текст джерелаДисертації з теми "Sesquiterpene synthases"
Li, Amang. "Investigations into the function of two plant sesquiterpene synthases : d-cadinene synthase and (e)-beta-farnesene synthase." Thesis, Cardiff University, 2011. http://orca.cf.ac.uk/55131/.
Повний текст джерелаGreenhagen, Bryan T. "ORIGINS OF ISOPRENOID DIVERSITY: A STUDY OF STRUCTURE-FUNCTION RELATIONSHIPS IN SESQUITERPENE SYNTHASES." UKnowledge, 2003. http://uknowledge.uky.edu/gradschool_diss/440.
Повний текст джерелаCouillaud, Julie. "The terpene mini-path : nouvel accès aux terpènes et exploration de l'espace chimique par une cascade enzymatique originale." Electronic Thesis or Diss., Aix-Marseille, 2021. http://www.theses.fr/2021AIXM0188.
Повний текст джерелаTo date, terpenoids form the most abundant and diversified class of natural products with more than 80,000 compounds whose structural, biological (antibiotic, anticancer, antimalarial, etc.) and physicochemical (flavor, fragrance, dye, etc.) properties hold the attention of the scientific community. However, their access is limited because of the low available quantity by extraction from natural sources; an often expensive and laborious chemical synthesis; and long biosynthetic pathways. By combining bioinformatic, statistical, biochemical and molecular biology approaches, we have developed the « Terpene mini-path », with only two enzymatic steps, as a synthetic and potentially bio-sourced alternative to access DMAPP and IPP, universal precursors of terpenes. This new artificial pathway allowed the synthesis of various natural and unnatural terpenoids, such as cyclobutylic derivatives, in the absence of any metabolic and enzymatic engineering. The mini-path provides thus an easy access to all terpenoids and represents an attractive new biosynthetic tool to explore the diversity of the terpene chemical space
Adams, Racheal. "Cloning and characterisation of (#EPSILON#) β farnesene synthase genes." Thesis, University of Nottingham, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.289464.
Повний текст джерелаKöllner, Tobias G. "Molekulare und genetische Aspekte der Biosynthese von komplexen Sesquiterpengemischen in Mais." kostenfrei, 2004. http://deposit.ddb.de/cgi-bin/dokserv?idn=972066292.
Повний текст джерелаAl-Lami, Naeemah. "Synthesis of nitrogen-containing bicyclic sesquiterpenes as potential transition state inhibitors of aristolochene synthase." Thesis, Cardiff University, 2013. http://orca.cf.ac.uk/53674/.
Повний текст джерелаAndersson, Marie. "Elucidation of the product synthesis of the sesquiterpene synthase Cop6 isolated from Coprinus cinereus." Thesis, Linköpings universitet, Institutionen för fysik, kemi och biologi, 2009. http://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-17252.
Повний текст джерелаHuh, Jung-Hyun. "Biochemical, Molecular and Functional Analysis of Volatile Terpene Formation in Arabidopsis Roots." Diss., Virginia Tech, 2011. http://hdl.handle.net/10919/77151.
Повний текст джерелаPh. D.
Singh, S. "Structural studies on sesquisabinene synthase 1: enzyme involved in terpene biosynthesis pathway." Thesis(Ph.D.), 2021. http://dspace.ncl.res.in:8080/xmlui/handle/20.500.12252/5995.
Повний текст джерелаHsieh, Hui-Ling, and 謝慧玲. "Cloning and Expression of a Sesquiterpene Synthase Gene from Taiwania cryptomerioides Hayata." Thesis, 2010. http://ndltd.ncl.edu.tw/handle/82143189020621256157.
Повний текст джерела國立臺灣大學
森林環境暨資源學研究所
98
Taiwania (Taiwania cryptomerioides Hayata) is a native conifer species of Taiwan. Many studies have demonstrated the bioactivities of secondary metabolites extracted from Taiwania in recent years. To regulate the biosynthsis of metabolites in Taiwania, it should be illustrate the synthesis based on the molecular level. In this study, we focus on sesquiterpene synthase of Taiwania. First, a pair of degenerated primers was designed for reverse transcription-polymerase chain reaction (RT-PCR) using total RNA extracted from leaves of mature tree. A DNA fragment with the conserved region of the terpene synthases (TPSs) was obtained. After 5’ and 3’ Rapid Amplification of cDNA Ends (RACE), the full-length cDNA was obtained, and it contains an open reading frame of 1791 bp with a predicated molecular mass of 70.2 kDa. The gene was highly expressed in young leaves, female flowers and cones. The expression in leave was enhanced after the treatment of soaking in 100 μM salicylic acid (SA). To identify the function of the obtained TPS, the recombinant protein from Escherichia coli was incubated with farnesyl diphosphate (FPP). After GC/MS analysis and retention time as well as mass spectrum matching with authentic standards revealed that the major product of TPS was sesquiterpene α-Gurjunene. The gene was named as Tc-Gur. To investigate the synthesis of this TPS in plant system, α-Gurjunene is also synthesized in transgenic Arabidopsis. But another sesquiterpene, α-Muurolene, is synthesized in transgenic hairy root of Taiwania.
Книги з теми "Sesquiterpene synthases"
Crock, John Edward. Five sesquiterpene synthases. 1998.
Знайти повний текст джерелаЧастини книг з теми "Sesquiterpene synthases"
Garrett, Steven R., Richard J. Morris, and Paul E. O'Maille. "Steady-State Kinetic Characterization of Sesquiterpene Synthases by Gas Chromatography–Mass Spectroscopy." In Natural Product Biosynthesis by Microorganisms and Plants, Part A, 3–19. Elsevier, 2012. http://dx.doi.org/10.1016/b978-0-12-394290-6.00001-x.
Повний текст джерелаHuynh, Florence, David J. Miller, and Rudolf K. Allemann. "Sesquiterpene Synthase-Catalyzed Conversion of a Farnesyl Diphosphate Analogue to a Nonnatural Terpenoid Ether." In Methods in Enzymology, 83–95. Elsevier, 2018. http://dx.doi.org/10.1016/bs.mie.2018.05.004.
Повний текст джерелаТези доповідей конференцій з теми "Sesquiterpene synthases"
Omar, Aimi Farehah, and Ismanizan Ismail. "Isolation of Persicaria minor sesquiterpene synthase promoter and its deletions for transgenic Arabidopsis thaliana." In THE 2016 UKM FST POSTGRADUATE COLLOQUIUM: Proceedings of the Universiti Kebangsaan Malaysia, Faculty of Science and Technology 2016 Postgraduate Colloquium. Author(s), 2016. http://dx.doi.org/10.1063/1.4966730.
Повний текст джерела