1994
DOI: 10.1039/c39940001281
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Evidence that the immediate biosynthetic precursor of clavulanic acid is its N-aldehyde analogue

Abstract: Clavulanate-9-aldehyde 1 has been detected in Streptomyces clavuligerus and an NADPH dependent dehydrogenase capable of reducing 1 to clavulanic acid 2 has been isolated from this organism.

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Cited by 46 publications
(41 citation statements)
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“…The organization and control of the genes associated with penam or cephem formation in vivo and the functions of these individual gene products have been intensively studied (11). In contrast, considerably less is known about the biosynthesis of clavulanic acid, although several intermediates have been identified (12,14) and three enzyme activities involved in the mid and late stages of the biosynthesis have been isolated and purified (12,14,26,32). Among these, clavaminate synthase (CS) is of particular importance.…”
mentioning
confidence: 99%
“…The organization and control of the genes associated with penam or cephem formation in vivo and the functions of these individual gene products have been intensively studied (11). In contrast, considerably less is known about the biosynthesis of clavulanic acid, although several intermediates have been identified (12,14) and three enzyme activities involved in the mid and late stages of the biosynthesis have been isolated and purified (12,14,26,32). Among these, clavaminate synthase (CS) is of particular importance.…”
mentioning
confidence: 99%
“…Clavaminic acid is thought to be the branch point of the pathway leading to clavulanic acid and the 5S clavams (10). The only other step known in the pathway beyond clavaminic acid is the reduction of clavaldehyde to clavulanic acid by the action of the enzyme clavulanic acid dehydrogenase (27), which is encoded by cad, a late gene from the clavulanic acid gene cluster (15). It is still not known how clavaminic acid is converted to clavaldehyde, nor have any of the steps specifically leading from clavaminic acid to the 5S clavams been elucidated (16).…”
mentioning
confidence: 99%
“…It synthesizes the ␤-lactam antibiotic cephamycin C, the ␤-lactamase inhibitor clavulanic acid, and several antifungal compounds with a clavam structure (for reviews, see references 3 and 15). The clavulanic acid biosynthesis pathway has several steps in common with the pathway for clavam biosynthesis (18,19). In addition to the compounds indicated above, S. clavuligerus produces the antibiotics holomycin and tunicamycin (10).…”
mentioning
confidence: 99%