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Review: a
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Review: (a) Phillips, D. R.; Rasbery, J. M.; Bartel, B.; Matsuda, S. P. T. Curr. Opin. Plant Biol. 2006, 9, 305-314.
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Curr. Opin. Plant Biol
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Phillips, D.R.1
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33748809553
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Subsequent reports on triterpene synthases: (b) Tansakul, P.; Shibuya, M.; Kushiro, T.; Ebizuka, Y. FEBS Lett. 2006, 580, 5143-5149.
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Subsequent reports on triterpene synthases: (b) Tansakul, P.; Shibuya, M.; Kushiro, T.; Ebizuka, Y. FEBS Lett. 2006, 580, 5143-5149.
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(c) Sawai, S.; Shindo, T.; Sato, S.; Kaneko, T.; Tabata, S.; Ayabe, S.-i.; Aoki, T. Plant Sci. 2006, 170, 247-257.
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Sawai, S.1
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Aoki, T.7
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33750689113
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(d) Basyuni, M.; Oku, H.; Inafuku, M.; Baba, S.; Iwasaki, H.; Oshiro, K.; Okabe, T.; Shibuya, M.; Ebizuka, Y. Phytochemistry 2006, 67, 2517-2524.
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(e) Shibuya, M.; Xiang, T.; Katsube, Y.; Otsuka, M.; Zhang, H.; Ebizuka, Y. J. Am. Chem. Soc. 2007, 129, 1450-1455.
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(f) Xiang, T.; Shibuya, M.; Katsube, Y.; Tsutsumi, T.; Otsuka, M.; Zhang, H.; Masuda, K.; Ebizuka, Y. Org. Lett. 2006, 8, 2835-2838.
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(g) Kolesnikova, M. D.; Obermeyer, A. C.; Wilson, W. K.; Lynch, D. A.; Xiong, Q.; Matsuda, S. P. T. Org. Lett. 2007, 9, 2183-2186.
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Kolesnikova, M.D.1
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(h) Lodeiro, S.; Xiong, Q.; Wilson, W. K.; Kolesnikova, M. D.; Onak, C. S.; Matsuda, S. P. T. J. Am. Chem. Soc. 2007, 129, 11213-11222.
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Reviews: a
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Reviews: (a) Wendt, K. U.; Schulz, G. E.; Corey, E. J.; Liu, D. R. Angew. Chem., Int. Ed. 2000, 39, 2812-2833.
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(b) Xu, R.; Fazio, G. C.; Matsuda, S. P. T. Phytochemistry 2004, 65, 261-290.
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Xu, R.1
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Husselstein-Muller, T.; Schaller, H.; Benveniste, P. Plant Mol. Biol. 2001, 45, 75-92.
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Husselstein-Muller, T.1
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33646124608
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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.
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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.
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(a) Hart, E. A.; Hua, L.; Darr, L. B.; Wilson, W. K.; Pang, J.; Matsuda, S. P. T. J. Am. Chem. Soc. 1999, 121, 9887-9888.
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J. Am. Chem. Soc
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Hart, E.A.1
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For details, see: b, Ph.D. Thesis, Rice University
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For details, see: (b) Hua, L. Ph.D. Thesis, Rice University, 2000, p 76.
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Hua, L.1
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0029944635
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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.
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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.
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2442615925
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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.
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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.
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37249067315
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Analysis of Sterols; Blackie (Chapman & Hall): London
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Goad, L. J.; Akihisa, T. Analysis of Sterols; Blackie (Chapman & Hall): London, 1997; appendix 3, section (h).
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appendix 3, section (h)
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Goad, L.J.1
Akihisa, T.2
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20
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0034628229
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We favor in vitro yields because in vivo accumulation can distort the enzymatic product profile. See: a
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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.
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Org. Lett
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Hua, L.2
Matsuda, S.P.T.3
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32644440439
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(b) Lodeiro, S.; Wilson, W. K.; Shan, H.; Matsuda, S. P. T. Org. Lett. 2006, 8, 439-442.
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Org. Lett
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Lodeiro, S.1
Wilson, W.K.2
Shan, H.3
Matsuda, S.P.T.4
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37249061431
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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
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1a but because minor products were not quantitated and detection limits were not reported, quantitative measures of product specificity are unavailable.
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23
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37249086909
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1a three of which make fewer than four rings.
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1a three of which make fewer than four rings.
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24
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37249085881
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Protein sequence identities were calculated in MegAlign from pairwise alignments
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(b) Protein sequence identities were calculated in MegAlign from pairwise alignments.
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0034720958
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Matsuda, S. P. T.; Darr, L. B.; Hart, E. A.; Herrera, J. B. R.; McCann, K. E.; Meyer, M. M.; Pang, J.; Schepmann, H. G. Org. Lett. 2000, 2, 2261-2263.
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McCann, K.E.5
Meyer, M.M.6
Pang, J.7
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Data available at http://mpss.udel.edu/at/.
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Data available at http://mpss.udel.edu/at/.
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