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Enzymatic degradation of carrageenan by halophilic bacteria from South-West coast in India

机译:来自印度西南海岸嗜盐细菌的角叉菜胶的酶促降解

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Summary form only given. Carrageenase producing halophilic bacteria were isolated from seawater and sediment samples collected from the vicinity of seaweed meadow, all along the South West coast of India. Two isolates, YK-C-1 and YK-C-2, producing large amount of extracellular carrageenase were selected for purification of enzyme. Correlation study of enzyme production with growth curve of the aforesaid two bacterial isolates was also undertaken. Maximum enzyme production was observed during 24-32 hours of incubation. Storage stability of crude enzyme was studied with respect to temperature at 350C, 200C and in frozen condition. It was observed that the enzyme was quite stable even at 350C for 7 days. After this period, a reduction in activity by 41% and 33% was observed from both the strains respectively. The purification of enzyme using 75% ammonium sulphate saturation yielded 1.1 and 1.6 fold purification respectively. Specificity of enzyme towards kappa, iota and lambda carrageenan was also studied.
机译:摘要表格仅给出。从印度西南海岸的海水草地附近收集的海水和沉积物样品中分离出生产嗜氧丙基细菌的鹿茸。选择两种分离株,YK-C-1和YK-C-2,用于纯化酶的纯化酶。还采用了上述两种细菌分离株生长曲线的酶产生的相关性研究。在24-32小时的孵育期间观察到最大酶产生。在350℃,200℃和冷冻条件下,研究了粗酶的储存稳定性。观察到酶即使在350℃下酶均匀稳定7天。在此期间之后,分别从菌株中减少41%和33%。使用75%硫酸铵饱和度酶的纯化分别产生1.1和1.6倍净化。还研究了酶对κ,IOTA和λArlageenan的特异性。

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