1967
DOI: 10.1016/0006-291x(67)90331-2
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Hydroxamate formation by anthranilate synthetase of Escherichia coli K12

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Cited by 14 publications
(3 citation statements)
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“…The hydroxamate assay procedure of Somerville and Elford (20) and Woolfolk, Shapiro, and Stadtman (23) was used to measure the hydroxamic acid formed by anthranilate synthetase. The reaction mixture contained, in a total volume of 0.9 ml: 40 jAmoles of L-glutamine, 80 j,moles of Tris, pH 7.8, 10,umoles of MgCl2, 200 jAmoles of freshly neutralized hydroxylamine, 0.4,Amole of chorismic acid, water, and enzyme to volume.…”
Section: Coonmentioning
confidence: 99%
“…The hydroxamate assay procedure of Somerville and Elford (20) and Woolfolk, Shapiro, and Stadtman (23) was used to measure the hydroxamic acid formed by anthranilate synthetase. The reaction mixture contained, in a total volume of 0.9 ml: 40 jAmoles of L-glutamine, 80 j,moles of Tris, pH 7.8, 10,umoles of MgCl2, 200 jAmoles of freshly neutralized hydroxylamine, 0.4,Amole of chorismic acid, water, and enzyme to volume.…”
Section: Coonmentioning
confidence: 99%
“…Isolation of y-glutamyl hydroxamate (55,56) following incubation of the enzyme with chorismate, glutamine, and hydroxylamine provides evidence for a y-glutamyl-enzyme thioester. Hydroxamate formation, dependent upon chorismate and indicative of glutaminase, has been detected with anthranilate synthetase from E. coli (57) and P. putida (33).…”
Section: Mechanism Of Glutamine Utilizationmentioning
confidence: 99%
“…However chemical intermediates have not been identified. The only partial reaction detected is glutaminase (20,57) which appears to be associated with the mechanism of glutamine utilization (Section IV). Formation of a-carboxy-a-Ndimethylnitrone by reaction of N-methyl hydroxylamine with the enolpyruvyl group of chorismate or with pyruvate may (55) or may not (56) be enzymatic and is of unknown significance.…”
Section: Conversion Of Chorismate To Anthranilatementioning
confidence: 99%