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Volumn 9, Issue 25, 2007, Pages 5223-5226

Arabidopsis camelliol C synthase evolved from enzymes that make pentacycles

Author keywords

[No Author keywords available]

Indexed keywords

CAMELLIOL C; HETEROCYCLIC COMPOUND; TRITERPENE; UNCLASSIFIED DRUG;

EID: 37249011225     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol702399g     Document Type: Article
Times cited : (41)

References (34)
  • 2
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    • Subsequent reports on triterpene synthases: (b) Tansakul, P.; Shibuya, M.; Kushiro, T.; Ebizuka, Y. FEBS Lett. 2006, 580, 5143-5149.
    • Subsequent reports on triterpene synthases: (b) Tansakul, P.; Shibuya, M.; Kushiro, T.; Ebizuka, Y. FEBS Lett. 2006, 580, 5143-5149.
  • 12
    • 33646124608 scopus 로고    scopus 로고
    • The only other oxidosqualene cyclase reported to make fewer than three rings is marnerai synthase (MRN1), which constructs a bicyclic cation that undergoes Grob fragmentation to the seco-A product (technically a monocycle): Xiong, Q.; Wilson, W. K.; Matsuda, S. P. T. Angew. Chem., Int. Ed. 2006, 45, 1285-1288.
    • The only other oxidosqualene cyclase reported to make fewer than three rings is marnerai synthase (MRN1), which constructs a bicyclic cation that undergoes Grob fragmentation to the seco-A product (technically a monocycle): Xiong, Q.; Wilson, W. K.; Matsuda, S. P. T. Angew. Chem., Int. Ed. 2006, 45, 1285-1288.
  • 14
    • 37249080452 scopus 로고    scopus 로고
    • For details, see: b, Ph.D. Thesis, Rice University
    • For details, see: (b) Hua, L. Ph.D. Thesis, Rice University, 2000, p 76.
    • (2000) , pp. 76
    • Hua, L.1
  • 15
    • 0029944635 scopus 로고    scopus 로고
    • SMY8 is a lanosterol synthase deletion mutant that accumulates the substrate oxidosqualene and consequently supports in vivo biosynthesis: Corey, E. J.; Matsuda, S. P. T.; Baker, C. H.; Ting, A. Y.; Cheng, H. Biochem. Biophys. Res. Commun. 1996, 219, 327-331.
    • SMY8 is a lanosterol synthase deletion mutant that accumulates the substrate oxidosqualene and consequently supports in vivo biosynthesis: Corey, E. J.; Matsuda, S. P. T.; Baker, C. H.; Ting, A. Y.; Cheng, H. Biochem. Biophys. Res. Commun. 1996, 219, 327-331.
  • 16
    • 2442615925 scopus 로고    scopus 로고
    • RXY6 is a squalene epoxidase/lanosterol synthase double deletion mutant that is useful for in vitro work because it cannot generate oxidosqualene: Fazio, G. C.; Xu, R.; Matsuda, S. P. T. J. Am. Chem. Soc. 2004, 126, 5678-5679.
    • RXY6 is a squalene epoxidase/lanosterol synthase double deletion mutant that is useful for in vitro work because it cannot generate oxidosqualene: Fazio, G. C.; Xu, R.; Matsuda, S. P. T. J. Am. Chem. Soc. 2004, 126, 5678-5679.
  • 19
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    • Analysis of Sterols; Blackie (Chapman & Hall): London
    • Goad, L. J.; Akihisa, T. Analysis of Sterols; Blackie (Chapman & Hall): London, 1997; appendix 3, section (h).
    • (1997) appendix 3, section (h)
    • Goad, L.J.1    Akihisa, T.2
  • 20
    • 0034628229 scopus 로고    scopus 로고
    • We favor in vitro yields because in vivo accumulation can distort the enzymatic product profile. See: a
    • We favor in vitro yields because in vivo accumulation can distort the enzymatic product profile. See: (a) Joubert, B. M.; Hua, L.; Matsuda, S. P. T. Org. Lett. 2000, 2, 339-341.
    • (2000) Org. Lett , vol.2 , pp. 339-341
    • Joubert, B.M.1    Hua, L.2    Matsuda, S.P.T.3
  • 22
    • 37249061431 scopus 로고    scopus 로고
    • Several other cyclases have qualitatively high product ratios, 1a but because minor products were not quantitated and detection limits were not reported, quantitative measures of product specificity are unavailable
    • 1a but because minor products were not quantitated and detection limits were not reported, quantitative measures of product specificity are unavailable.
  • 23
    • 37249086909 scopus 로고    scopus 로고
    • 1a three of which make fewer than four rings.
    • 1a three of which make fewer than four rings.
  • 24
    • 37249085881 scopus 로고    scopus 로고
    • Protein sequence identities were calculated in MegAlign from pairwise alignments
    • (b) Protein sequence identities were calculated in MegAlign from pairwise alignments.
  • 27
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    • Data available at http://mpss.udel.edu/at/.
    • Data available at http://mpss.udel.edu/at/.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.