Prajapati Vimal S, Trivedi Ujjval B, Patel Kamlesh C
BRD School of Biosciences, Sardar Patel University, Sardar Patel Maidan, Vadtal Road, Satellite Campus, Post Box No. 39, Vallabh Vidyanagar, 388-120, Gujarat, India.
3 Biotech. 2015 Apr;5(2):211-220. doi: 10.1007/s13205-014-0213-1. Epub 2014 Apr 11.
The bacterial strain producing thermostable, alklophilic alpha-amylase was identified as Bacillus amyloliquefaciens KCP2 using 16S rDNA gene sequencing data (NCBI Accession No: KF112071). Medium components were optimized through the statistical approach for the synthesis of alpha-amylase by the organism under solid-state fermentation using wheat bran as the substrate. The medium components influencing the enzyme production were identified using a two-level fractional factorial Plackett-Burman design. Among the various variables screened, starch, ammonium sulphate and calcium chloride were found to be most significant medium components. The optimum levels of these significant parameters were determined employing the response surface Central Composite design which significantly increased the enzyme production with the supplementation of starch 0.01 g, ammonium sulphate 0.2 g and 5 mM calcium chloride in the production medium. Temperature and pH stability of the alpha-amylase suggested its wide application in the food and pharmaceutical industries.
利用16S rDNA基因测序数据(NCBI登录号:KF112071),将产热稳定嗜碱α-淀粉酶的菌株鉴定为解淀粉芽孢杆菌KCP2。采用统计方法优化培养基成分,以麦麸为底物,在固态发酵条件下由该菌株合成α-淀粉酶。使用二级部分因子Plackett-Burman设计确定影响酶产量的培养基成分。在筛选的各种变量中,淀粉、硫酸铵和氯化钙被发现是最显著的培养基成分。采用响应面中心复合设计确定这些显著参数的最佳水平,在生产培养基中添加0.01 g淀粉、0.2 g硫酸铵和5 mM氯化钙后,酶产量显著提高。α-淀粉酶的温度和pH稳定性表明其在食品和制药行业具有广泛应用。