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Volumn 122, Issue 28, 2000, Pages 6765-6766

A tyrosine-to-threonine mutation converts cycloartenol synthase to an oxidosqualene cyclase that forms lanosterol as its major product [1]

Author keywords

[No Author keywords available]

Indexed keywords

LANOSTEROL SYNTHASE; SQUALENE DERIVATIVE;

EID: 0034686761     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja0013226     Document Type: Letter
Times cited : (56)

References (26)
  • 12
    • 0343545195 scopus 로고    scopus 로고
    • note
    • Arabidopsis thaliana cycloartenol synthase numbering is used, with the corresponding conserved lanosterol synthase residue in parentheses.
  • 14
    • 0342675028 scopus 로고    scopus 로고
    • note
    • The lanosterol synthase mutation in LHY4 ensures that any observed activity results from the recombinant gene. In addition, the squalene synthase mutation precludes in vivo triterpene biosynthesis, preventing the accumulation of compounds that would otherwise skew apparent product ratios by contributing to the isolated yields.
  • 24
    • 0343545190 scopus 로고    scopus 로고
    • note
    • Concerted reactions without discrete C-8 or C-9 cations or elimination from a C-8, C-9 bridged structure are also plausible.
  • 26
    • 0000680597 scopus 로고    scopus 로고
    • Excerpta Medica International Congress Series 1157; Ageta, H., Aimi, N., Ebizuka, Y., Fujita, T., Honda, G., Eds.; Elsevier Science: Amsterdam
    • Kushiro, T.; Shibuya, M.; Ebizuka, Y. In Towards Natural Medicine Research in the 21st Century, Excerpta Medica International Congress Series 1157; Ageta, H., Aimi, N., Ebizuka, Y., Fujita, T., Honda, G., Eds.; Elsevier Science: Amsterdam, 1998; pp 421-428.
    • (1998) Towards Natural Medicine Research in the 21st Century , pp. 421-428
    • Kushiro, T.1    Shibuya, M.2    Ebizuka, Y.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.