Pyrrole-2-carboxylate decarboxylase from Bacillus megaterium PYR2910, an organic-acid-requiring enzyme
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چکیده
منابع مشابه
Enzyme localization in Bacillus megaterium.
Weibull (1953a) has shown that after osmotic lysis of protoplasts of Bacillus megaterium, prepared by controlled treatment with lysozyme, only two microscopically detectable structures remain; membrane-like bodies termed "ghosts," and granules. The ghosts were found to sediment as a dark yellow fraction by centrifugation at 10,000 G (Weibull, 1953b) and to contain almost all the pigmented mater...
متن کاملtert-Butyl 2-(dihydroxyboryl)pyrrole-1-carboxylate
In the title compound, C(9)H(14)BNO(4), the carbonyl and boronic acid groups are essentially coplanar with the pyrrole ring and the boronic acid group has an exo-endo conformation. The exo-oriented OH is engaged in an intra-molecular O-H⋯O inter-action, while the endo-oriented one is involved in inter-molecular hydrogen bonding to form centrosymmetric dimers. A supra-molecular assembly is achie...
متن کاملInduced release of dipicolinic acid from spores of Bacillus megaterium.
Conditions under which dipicolinic acid may be released from bacterial spores probably relate to the chemical state of the dipicolinic acid in the spore, to its physical location in the spore, and to its influence on the physiological properties of the spore. The latter aspect embraces the relation between release of dipicolinic acid and the viability of the spore, its heat resistance, and its ...
متن کاملBiosynthesis of dipicolinic acid in Bacillus megaterium.
Very little is known of the precursors of the dipicolinic acid (pyridine-2,6-dicarboxylic acid) in bacterial spores. C'4-2,6-diaminopimelic acid was shown to contribute to the formation of dipicolinic acid in Bacillus cereus var. mycoides (Perry and Foster, 1955; Foster, 1956) but the efficiency of the conversion was low, possibly because of a slow penetration of the cells by the exogenously su...
متن کاملEthyl 5-(4-Bromophenyl)-4-methyl-1H-pyrrole- 2-carboxylate
This note describes a sequence converting an oxime-substituted pyrrolidine into a trisubstituted pyrrole structure. The synthetic route is based on a double chlorination of the pyrrolidine substrate followed by the base induced formation of both an imine and a nitrile oxide functionality. The latter reacts with an immobilized thiourea to yield an isothiocyanate which upon elimination generates ...
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ژورنال
عنوان ژورنال: European Journal of Biochemistry
سال: 1998
ISSN: 0014-2956,1432-1033
DOI: 10.1046/j.1432-1327.1998.2530480.x