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Glycine genera

Table 1.3. The Genus Glycine, 3-Letter Code, 2n Number, Genome, and Distribution ... Table 1.3. The Genus Glycine, 3-Letter Code, 2n Number, Genome, and Distribution ...
Fig. 1.1. Geographical origin of the genus Glycine. Adapted from Hymowitz, 2004. Fig. 1.1. Geographical origin of the genus Glycine. Adapted from Hymowitz, 2004.
Domagalski, J.M. K.O. Kollipara A.H. Bates D.L. Brandon M. Friedman T. Hymowitz. Nulls for the major Bowman-Birk protease inhibitor in the genus. Glycine. Crop Sci. 1992, 32, 1502-1505. [Pg.31]

Hymowitz, T. C.A. Newell. Taxonomy, speciation, domestication, dissemination, germplasm resources and variation in the genus Glycine. Advances in Legume Science R.J. Summerfield, A.H. Bunting, Eds. Royal Botanic Gardens Kew, England, 1980 pp.251-264. [Pg.33]

Lim, S.M. T. Hymowitz. Reactions of perennial wild species of genus Glycine to Septoria glycines. Plant Dis. 1987,17, 891-893. [Pg.34]

The soya bean plant (genus Glycine , species Mar, family Leguminosae , subfamily Papilionoideae) is a bush-like aimual, growing about 1.8 m tall and bearing pods which each contain several smooth seeds - the soya beans. It... [Pg.398]

Soybeans belong to the pea family, Leguminosae. It is classed as genus Glycine, species G. max. [Pg.976]

Hymowitz, T., Palmer, R. G., and Hadley, H. H., 1972, Seed weight, protein, oil and fatty acid relationships within the genus Glycine, Trop. [Pg.676]

Stickland LH (1935b) Studies in the metabolism of the strict anaerobes (genus Clostridium). III. The oxidation of alanine by Cl. sporogenes. IV. The reduction of glycine by Cl. sporogenes. Biochem J 29 898. [Pg.334]

Several deadly species of the genus Amanita produce colorless toxic octapeptides, the amani-tins.a b Two residues of glycine, one of L-isoleucine, one of the unusual L-dihydroxyisoleucine, one of L-asparagine, and one of L-hydroxyproline are present in a-amanitin. In the center a modified tryptophan residue has been combined oxidatively with an SH group of a cysteine residue. If the dihy-droxyisoleucine residue of a-amanitin is replaced with unhydroxylated leucine, the resulting compound, known as amanullin, is nontoxic. The LD50 for mice is 0.3 mg kg 1 and 50 g of fresh Amanita phalloides may be sufficient to kill a person. Arnan-itins act slowly, and it is impossible to kill mice in less than 15 h, no matter how high the dose. [Pg.1625]


See other pages where Glycine genera is mentioned: [Pg.1655]    [Pg.253]    [Pg.9]    [Pg.9]    [Pg.11]    [Pg.12]    [Pg.13]    [Pg.15]    [Pg.15]    [Pg.15]    [Pg.28]    [Pg.32]    [Pg.37]    [Pg.53]    [Pg.1655]    [Pg.253]    [Pg.9]    [Pg.9]    [Pg.11]    [Pg.12]    [Pg.13]    [Pg.15]    [Pg.15]    [Pg.15]    [Pg.28]    [Pg.32]    [Pg.37]    [Pg.53]    [Pg.305]    [Pg.257]    [Pg.1785]    [Pg.493]    [Pg.87]    [Pg.145]    [Pg.115]    [Pg.473]    [Pg.28]    [Pg.566]    [Pg.81]    [Pg.390]    [Pg.869]    [Pg.59]    [Pg.67]    [Pg.73]    [Pg.712]    [Pg.872]    [Pg.11]    [Pg.12]    [Pg.12]    [Pg.13]   


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