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Literature summary for 2.1.1.142 extracted from

  • Holmberg, N.; Harker, M.; Wallace, A.D.; Clayton, J.C.; Gibbard, C.L.; Safford, R.
    Co-expression of N-terminal truncated 3-hydroxy-3-methylglutaryl CoA reductase and C24-sterol methyltransferase type 1 in transgenic tobacco enhances carbon flux towards end-product sterols (2003), Plant J., 36, 12-20.
    View publication on PubMed

Cloned(Commentary)

Cloned (Comment) Organism
coexpression of the catalytic domain of Hevea brasiliensis 3-hydroxy-3-methylglutaryl CoA reductase and Nicotiana tabacum C24-sterol methyltransferase type 1 in tobacco, under control of both constitutive and seed-specific promoters, resulting in increased accumulation of total sterol in seed tissue by 2.5fold and 2.1fold, respectively Nicotiana tabacum

Natural Substrates/ Products (Substrates)

Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
S-adenosyl-L-methionine + 5alpha-cholesta-8,24-dien-3beta-ol Nicotiana tabacum 3-hydroxy-3-methylglutaryl CoA reductase and C24-sterol methyltransferase type 1 work in concert to control carbon flux into end-product sterols. Sterol composition can be controlled by the temporal activity of the promoters driving transgene expression S-adenosyl-L-homocysteine + 24-methylene-5alpha-cholest-8-en-3beta-ol
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Organism

Organism UniProt Comment Textmining
Nicotiana tabacum
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Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
S-adenosyl-L-methionine + 5alpha-cholesta-8,24-dien-3beta-ol 3-hydroxy-3-methylglutaryl CoA reductase and C24-sterol methyltransferase type 1 work in concert to control carbon flux into end-product sterols. Sterol composition can be controlled by the temporal activity of the promoters driving transgene expression Nicotiana tabacum S-adenosyl-L-homocysteine + 24-methylene-5alpha-cholest-8-en-3beta-ol
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Synonyms

Synonyms Comment Organism
C24-sterol methyltransferase type 1
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Nicotiana tabacum
SMT1
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Nicotiana tabacum