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Exoprotease activity of Leuconostoc oenos in stress conditions

机译:应激条件下亮光褐藻的外切蛋白酶活性

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Exoprotease activity during 48 h of total energy and nutrient starvation was examined in Leuconostoc oenos X2L isolated from wine. Starved cells after 2 h of incubation at 30 degrees C in citrate buffer, 0.05 mmol l(-1) pH 5, showed greater extracellular proteolytic activity than at the onset of starvation. In the presence of 60 mg l(-1) SO2 and 8% or 12% ethanol, the proteolytic activity was higher; 10 mmol l(-1) Ca2+ and Mg2+ produced an increase in protease activity during starvation. Glucose and 2-deoxyglucose (2-DOG) were found to repress synthesis by 80% and 100%, respectively. Cyclic adenosine 3'-5'-phosphate increased the exoprotease activity and reverted the repression by glucose and 2-DOG. De novo synthesis of proteins was required for the exoprotease activity by cells submitted to stress conditions. The absence of protease activity in the supernatant fluids from chloramphenicol-treated cells indicated that the activity is a result of deliberate release and not of passive cell lysis.
机译:在从葡萄酒中分离出的Leuconostoc oenos X2L中检测了48小时总能量和营养缺乏状态下的蛋白酶活性。在30°C的柠檬酸缓冲液(0.05 mmol l(-1)pH 5)中孵育2小时后,饥饿的细胞显示出比饥饿开始时更大的细胞外蛋白水解活性。在60 mg l(-1)SO2和8%或12%乙醇的存在下,蛋白水解活性更高。 10 mmol l(-1)Ca2 +和Mg2 +在饥饿期间产生了蛋白酶活性的增加。发现葡萄糖和2-脱氧葡萄糖(2-DOG)分别抑制合成80%和100%。环状腺苷3'-5'-磷酸增加外切蛋白酶的活性,并恢复葡萄糖和2-DOG的阻遏作用。从头合成蛋白质是细胞承受应激条件下外切蛋白酶活性所必需的。氯霉素处理过的细胞的上清液中没有蛋白酶活性,表明该活性是故意释放而不是被动细胞裂解的结果。

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