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Heat induced translocation of proteins and enzymes within the cell:an effective way to optimize the microbial cell disruption process

机译:热诱导细胞内蛋白质和酶的移位:优化微生物细胞破坏过程的有效方法

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The energy efficiency of the cell disruption process for the recovery of intracellular proteins depends on the physical strength of the cell wall of the microorganism and on the intracellular location of the target enzymes,also the way in which the stress is applied(effectiveness).Heat stress was found to induce translocation of the target enzyme(beta-galactosidase)and also to promote aggregation of the total protein leached out in the suspension after their translocation.Translocation provides an external means to reduce the severity of the cell disruption process and reduction in the energy requirements for the same.This aggregated protein could be removed by centrifugation prior to cell disruption.Thus,the purity and selectivity of the target enzyme could be substantially improved,along with a reduction in the energy required for disruption,by subjecting cells to heat stress.The kinetics of translocation are reported and depend on variation in location factor(LF),possibly enabling the heat treatment protocol to be optimized.
机译:用于破坏细胞内蛋白质的细胞破坏过程的能量效率取决于微生物细胞壁的物理强度以及目标酶在细胞内的位置,还取决于施加压力的方式(有效性)。发现应激可以诱导目标酶(β-半乳糖苷酶)的转运,并促进转运后悬浮液中浸出的总蛋白的聚集。通过破坏细胞之前可通过离心去除这种聚集的蛋白质。因此,通过使细胞受到干扰,可以大大提高目标酶的纯度和选择性,同时减少破坏所需的能量。据报道,易位动力学取决于位置因子(LF)的变化,可能使他的热处理方案有待优化。

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