Schräder T, Andreesen J R
Institut für Mikrobiologie, Universität Halle, Germany.
Appl Microbiol Biotechnol. 1996 May;45(4):458-64. doi: 10.1007/BF00578456.
Inactivation of D-amino acid oxidase occurred by different mechanisms. The enzyme showed a rapid loss of activity in the presence of micromolar amounts of Cu2+ and Hg2+. It was also sensitive to oxidative inactivation by Fe2+ and H2O2 when both reagents were added in millimolar amounts. When oxidatively inactivated D-amino acid oxidase and a corresponding non-treated control were modified with the sulfhydryl-modifying, fluorescent reagent monobromobimane and subsequently digested with endoproteinase Glu-C, Cys-298 was identified to be a target for oxidative modification according to differences in the known peptide profile of fluorescence intensity. Another reason for the observed loss of enzyme activity in crude extracts was the specific proteolytic digestion of D-amino acid oxidase, which was dependent on the growth phase of the cells used. This cleavage was catalyzed by a serine-type proteinase and was the introductory step for the further complete degradation of the enzyme. In addition, a coenriched 50-kDa protein, identified as NADPH-specific glutamate dehydrogenase, significantly decreased the stability of the D-amino acid oxidase activity. Treatment of apo-D-amino acid oxidase from T. variabilis with monobromobimane resulted in a significantly increased fluorescence of two peptides, neither of which contained any cysteine residue. Thus, an involvement of cysteine residues in binding the FAD coenzyme should be excluded.
D-氨基酸氧化酶的失活是由不同机制引起的。在存在微摩尔量的Cu2+和Hg2+时,该酶活性迅速丧失。当以毫摩尔量添加Fe2+和H2O2时,它对氧化失活也很敏感。当用巯基修饰的荧光试剂单溴联苯胺对氧化失活的D-氨基酸氧化酶和相应的未处理对照进行修饰,随后用内肽酶Glu-C消化时,根据已知的荧光强度肽谱差异,确定Cys-298是氧化修饰的靶点。粗提物中观察到的酶活性丧失的另一个原因是D-氨基酸氧化酶的特异性蛋白水解消化,这取决于所用细胞的生长阶段。这种切割由丝氨酸型蛋白酶催化,是该酶进一步完全降解的起始步骤。此外,一种共同富集的50 kDa蛋白质,被鉴定为NADPH特异性谷氨酸脱氢酶,显著降低了D-氨基酸氧化酶活性的稳定性。用单溴联苯胺处理可变嗜热栖热菌的脱辅基D-氨基酸氧化酶,导致两种肽的荧光显著增加,这两种肽均不包含任何半胱氨酸残基。因此,应排除半胱氨酸残基参与结合FAD辅酶的可能性。