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Adenosine-5′-Phosphosulfate- and Sulfite Reductases Activities of Sulfate-Reducing Bacteria from Various Environments

机译:不同环境中硫酸盐还原菌的腺苷5-磷酸和亚硫酸盐还原酶活性

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摘要

A comparative study of the kinetic characteristics (specific activity, initial and maximum rate, and affinity for substrates) of key enzymes of assimilatory sulfate reduction (APS reductase and dissimilatory sulfite reductase) in cell-free extracts of sulphate-reducing bacteria (SRB) from various biotopes was performed. The material for the study represented different strains of SRB from various ecotopes. Microbiological (isolation and cultivation), biochemical (free cell extract preparation) and chemical (enzyme activity determination) methods served in defining kinetic characteristics of SRB enzymes. The determined affinity data for substrates (i.e., sulfite) were 10 times higher for SRB strains isolated from environmental (soil) ecotopes than for strains from the human intestine. The maximum rate of APS reductase reached 0.282–0.862 µmol/min×mg of protein that is only 10 to 28% higher than similar initial values. The maximum rate of sulfite reductase for corrosive relevant collection strains and SRB strains isolated from heating systems were increased by 3 to 10 times. A completely different picture was found for the intestinal SRB V in the strains Vib-7 (0.67 µmol/min × mg protein) and Rod-9 (0.45 µmol/min × mg protein). The determinant in the cluster distribution of SRB strains is the activity of the terminal enzyme of dissimilatory sulfate reduction—sulfite reductase, but not APS reductase. The data obtained from the activity of sulfate reduction enzymes indicated the adaptive plasticity of SRB strains that is manifested in the change in enzymatic activity.
机译:无细胞硫酸盐还原细菌(SRB)提取物中同化硫酸盐还原关键酶(APS还原酶和异化亚硫酸盐还原酶)的动力学特性(比活,初始和最大速率以及对底物的亲和力)的动力学特性的比较研究进行了各种生物表位。研究的材料代表了来自不同生态环境的不同SRB菌株。微生物(分离和培养),生化(游离细胞提取物制备)和化学(酶活性测定)方法可用于定义SRB酶的动力学特征。从环境(土壤)生态位分离出的SRB菌株对底物(即亚硫酸盐)的亲和力数据要比从人肠中分离的亲和力数据高10倍。 APS还原酶的最大速率达到0.282–0.862 µmol / min×mg的蛋白质,仅比相似的初始值高10%至28%。从加热系统中分离出的腐蚀性相关收集菌株和SRB菌株的亚硫酸盐还原酶的最大速率提高了3到10倍。在Vib-7(0.67 µmol / min×mg蛋白)和Rod-9(0.45 µmol / min×mg蛋白)菌株中,肠道SRB V的情况完全不同。 SRB菌株簇分布的决定因素是异化硫酸盐还原的末端酶的活性-亚硫酸盐还原酶,而不是APS还原酶。从硫酸盐还原酶的活性获得的数据表明,SRB菌株的适应性可塑性表现为酶活性的变化。

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