首页> 外文期刊>Journal of Rapid Methods and Automation in Microbiology >alpha -AMYLASE SYNTHESIS BY MUTANT OF BACILLUS SUBTILIS IMMOBILIZED ONTO CHANNEL ALUMINA BEADS
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alpha -AMYLASE SYNTHESIS BY MUTANT OF BACILLUS SUBTILIS IMMOBILIZED ONTO CHANNEL ALUMINA BEADS

机译:固定在通道氧化铝珠上的芽孢杆菌突变体合成α-淀粉酶

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ABSTRACTS: A W sub(20)mutant strain derived from Bacillus subtilis H sub(1)using UV radiation and exposure to a mutagenic agent was used for alpha -amylase synthesis. Both cultures were characterized for growth and continuous alpha -amylase syntheses, and the isolated enzymes had the same molecular mass of similar to 55 kDa. W sub(20)cells, harvested from specific growth phase, were immobilized within alumina beads and placed in a bioreactor column; specific feedstock (FS) was used for alpha -amylase syntheses and was affected by its composition, and its flow rate as well as temperature. Maximal alpha -amylase productivity (427- mu M reducing sugar[s]-mL effluent-h) was achieved using stationary-phase cells and FS containing 3% starch kept at 45C and 100-mL-h flow rate. When FS, with 2% starch, was fed to the column at the same temperature but at a higher flow rate, productivities were reduced to 326 mu M. alpha -amylase synthesis by W sub(20)cells was affected by growth phase of cells used, column temperature and FS flow rate. Some immobilized cells were washed out from the column because of shear forces on bead surfaces by FS flow rate and by temperature. Scanning electron micrographs revealed large numbers of cells attached to external and internal bead channels. This article is a novel approach for alpha -amylase synthesis and can be used for its industrial production.
机译:摘要:使用紫外线辐射并暴露于诱变剂的枯草芽孢杆菌H sub(1)衍生的W sub(20)突变株用于α-淀粉酶合成。两种培养物均具有生长和连续α-淀粉酶合成的特征,并且分离的酶具有相同的分子量,类似于55 kDa。从特定生长期收获的W sub(20)细胞被固定在氧化铝珠中,并置于生物反应器柱中;特定原料(FS)用于合成α-淀粉酶,并受其组成,流速和温度的影响。使用固定相细胞和含有3%淀粉的FS保持在45°C和100-mL-h的流速下,可获得最大的α-淀粉酶生产率(427-μM还原糖[s] -mL流出物-h)。当将具有2%淀粉的FS以相同的温度但以较高的流速进料到色谱柱中时,生产率降低到326μM。W sub(20)细胞的α-淀粉酶合成受到细胞生长阶段的影响使用的色谱柱温度和FS流速。由于通过FS流速和温度对珠子表面的剪切力,一些固定化的细胞从色谱柱上洗掉了。扫描电子显微照片显示大量细胞附着在外部和内部的珠子通道上。本文是用于α-淀粉酶合成的新方法,可用于其工业生产。

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