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Enzymes of Krebs-Henseleit Cycle in Vitis vinifera L
Author(s) -
Kalliopi A. Roubelakis,
W. M. Kliewer
Publication year - 1978
Publication title -
plant physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.554
H-Index - 312
eISSN - 1532-2548
pISSN - 0032-0889
DOI - 10.1104/pp.62.3.344
Subject(s) - in vivo , enzyme , arginine , incubation , arginase , in vitro , chemistry , hydrolysis , biochemistry , vitis vinifera , incubation period , molar concentration , enzyme assay , chromatography , biology , amino acid , botany , organic chemistry , microbiology and biotechnology
The presence of arginase (EC 3.5.3.7) in various tissues from Vitis vinifera L. cultivars was demonstrated by both in vivo and in vitro enzyme assays. Initial velocities determined by the two methods were in close agreement. Optimum conditions for maximum enzyme activity were 25 to 30 millimolar l-arginine, about 1 millimolar Mn(2+) (pH 9.4 to 9.8), and incubation temperature of 37 to 38 C. l-Arginine hydrolysis was linear with increasing sliced fresh tissue up to 500 milligrams for in vivo assay, and with enzyme extract equivalent up to about 200 milligrams of fresh tissue for in vitro. Similarly, l-arginine hydrolysis was linear with incubation time for the first 45 minutes for in vivo assay and for the first 20 minutes for in vitro.

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