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Isolation and Characterization of Gram-Positive Cyanophycin-Degrading Bacteria-Kinetic Studies on Cyanophycin Depolymerase Activity in Aerobic Bacteria

机译:革兰氏阳性蓝霉素降解细菌的分离和表征-好氧细菌蓝霉素解聚酶活性的动力学研究

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This study is the first report on the extracellular degradation of cyanophycin (CGP) by Gram-positive bacteria.Three different Gram-positive bacteria were isolated from forest soil that were able to utilize CGP as the sole carbon source for growth.The isolates were assigned to species of the genera Bacillus and Micromonospora.From one of the isolates,which was taxonomically affiliated as Bacillus megaterium strain BAG 19,the extracellular CGP depolymerase (extracellular CGPase; CphE_(Bm)) was purified to electrophoretic homogeneity by fast protein liquid chromatography and affinity binding to an arginine-agarose column.The purified enzyme was specific for hydrolytic cleavage of CGP,and inhibitor studies indicated that CphE_(Bm) is a serine-type peptidase.As CGP degradation products,(beta-Asp-Arg)_2 tetrapeptides in addition to beta-Asp-Arg dipeptides occurred,which were identified by electrospray ionization mass spectrometry analysis.Furthermore,a novel quantitative enzyme assay was developed for kinetic studies on CGP depolymerases.For CphE_(Bm),as well as for the extracellular CGPase of Pseudomonas anguilliseptica strain BI (CphE_(Pa)),K_M values of 2.2 and 1.0 muM,respectively,for CGP were determined.
机译:这项研究是关于革兰氏阳性细菌胞外降解蓝霉素(CGP)的第一份报告。从森林土壤中分离出三种不同的革兰氏阳性细菌,它们能够利用CGP作为唯一的碳源进行生长,并确定了分离株从一种分类学上属于巨大芽孢杆菌BAG 19的分离株中,通过快速蛋白质液相色谱法将细胞外CGP解聚酶(细胞外CGPase; CphE_(Bm))纯化至电泳同质性。亲和力结合到精氨酸-琼脂糖柱上。纯化的酶对CGP的水解裂解具有特异性,抑制剂研究表明CphE_(Bm)是一种丝氨酸肽酶。作为CGP的降解产物,β-Asp-Arg)_2四肽除了发生β-Asp-Arg二肽外,还通过电喷雾电离质谱分析法对其进行了鉴定。可以用于CGP解聚酶的动力学研究。对于CphE_(Bm)以及嗜酸假单胞菌BI菌株BI(CphE_(Pa))而言,对于CGP的K_M值分别确定为2.2和1.0μM。

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