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l tryptophan/tobak

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Tryptophan Biosynthesis in Cell Cultures of Nicotiana tabacum.

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Some of the general features of the pathway for l-tryptophan biosynthesis in cell cultures of Nicotiana tabccum var. Wisc. 38 have been investigated. The results of both isotope competition and direct-labeling experiments show that shikimic acid, anthranilic acid, indoleglycerol phosphate, and
UNASSIGNED Conifers contain P450 enzymes from the CYP79 family that are involved in cyanogenic glycoside biosynthesis. Cyanogenic glycosides are secondary plant compounds that are widespread in the plant kingdom. Their biosynthesis starts with the conversion of aromatic or aliphatic amino acids into

Mutants of Nicotiana plumbaginifolia with increased sensitivity to auxin.

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Two non-allelic, monogenic recessive mutations, aus1 and aus2, have been isolated which result in auxin hypersensitivity in mutant Nicotiana plumbaginifolia plants. At relatively low concentrations of indole-3-acetic acid or 1-naphthaleneacetic acid, the elongation growth of mutant seedling
Tryptophan decarboxylase (TDC) is a cytosolic enzyme that catalyzes an early step of the terpenoid indole alkaloid biosynthetic pathway by decarboxylation of L-tryptophan to produce the protoalkaloid tryptamine. In the present study, recombinant TDC was targeted to the chloroplast, cytosol, and
BACKGROUND Plants produce a group of aldoxime metabolites that are well known as volatiles and as intermediates in cyanogenic glycoside and glucosinolate biosynthesis in particular plant families. Recently it has been demonstrated that aldoximes can also accumulate as part of direct plant defense in

Regulation of sulfate uptake by amino acids in cultured tobacco cells.

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The sulfur requirements of tobacco (Nicotiana tabacum L. var. Xanthi) XD cells grown in chemically defined liquid media can be satisfied by sulfate, thiosulfate, l-cyst(e)ine, l-methionine or glutathione, and somewhat less effectively by d-cyst (e) ine, d-methionine or dl-homocyst (e)ine. Sulfate
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