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Application of Statistically Based Experimental Designs to Optimize Cellulase Production and Identification of Gene

机译:基于统计的实验设计在优化纤维素酶生产和基因鉴定中的应用

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摘要

AbstractA natural bacterial strain identified as Bacillus amyloliquefaciens MBAA3 using 16S rDNA partial genome sequencing has been studied for optimization of cellulase production. Statistical screening of media components for production of cellulase by B. amyloliquefaciens MBAA3 was carried out by Plackett–Burman design. Plackett–Burman design showed CMC, MgSO4 and pH as significant components influencing the cellulase production from the media components screened by Plackett-Burman fractional factorial design. The optimum concentrations of these significant parameters were determined employing the response surface central composite design, involving three factors and five levels was adopted to acquire the best medium for the production of cellulase enzyme revealed concentration of CMC (1.84 g), MgSO4 (0.275 g), and pH (8.5) in media for highest enzyme production. Response surface counter plots revealed that middle level of MgSO4 and middle level of CMC, higher level of CMC and lower level of pH and higher level of MgSO4 with lower level of pH increase the production of cellulase. After optimization cellulase activity increased by 6.81 fold. Presence of cellulase gene in MBAA3 was conformed by the amplification of genomic DNA of MBAA3. A PCR product of cellulase gene of 1500 bp was successfully amplified. The amplified gene was conformed by sequencing the amplified product and sequence was deposited in the gene bank under the accession number .
机译:摘要研究了使用16S rDNA部分基因组测序鉴定为解淀粉芽孢杆菌MBAA3的天然细菌菌株,以优化纤维素酶的生产。通过解淀粉芽孢杆菌MBAA3产生纤维素酶的培养基成分的统计筛选是通过Plackett-Burman设计进行的。 Plackett-Burman设计显示,CMC,MgSO4和pH是影响通过Plackett-Burman分数阶乘设计筛选的培养基成分产生纤维素酶的重要成分。这些重要参数的最佳浓度是通过响应表面中央复合设计确定的,涉及三个因素,并采用五个水平来获得用于生产纤维素酶的最佳培养基,从而揭示了CMC(1.84 g),MgSO4(0.275 g)的浓度,以及培养基中的pH值(8.5),以产生最高的酶。响应表面计数器图显示,MgSO 4的中间水平和CMC的中间水平,CMC的较高水平和pH的较低水平以及pH值较低的MgSO 4的较高水平增加了纤维素酶的产量。优化后,纤维素酶活性增加了6.81倍。 MBAA3中纤维素酶基因的存在通过MBAA3基因组DNA的扩增来证实。成功扩增了1500bp的纤维素酶基因的PCR产物。通过对扩增产物进行测序对扩增的基因进行整合,并将序列以登录号保存在基因库中。

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