固定化产气克雷伯菌产碱性蛋白酶的研究

M. Osho, G. Akhigbe, G. A. Adekoya
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摘要

本研究从乳化厂污水污泥中筛选碱性蛋白酶微生物,经16S核糖体RNA核苷酸序列鉴定为产气克雷伯菌,菌株编号为MF156964.1,最高鉴定率为95.45%。用椰壳固定化细胞,考察了不同粒径、pH、温度、搅拌速度和孵育时间对细胞固定化效果的影响。在筛选的23种微生物中,有3种是潜在的蛋白酶生产者。在脱脂乳琼脂平板上,产气克雷伯菌的水解区最高(35 mm)。粒径为0.075 mm2的固定化剂酶活最高,为176.83 U/mL。产生蛋白酶的最佳孵育时间为48 h,酶活性为143.054 U/mL,酶活性进一步下降。蛋白酶的最适pH为9.0,活性为209.61 U/mL,呈碱性。转速为150 rpm时,蛋白酶活性为175.83 U/mL,转速为250 rpm时,蛋白酶活性降低56.5%。最适温度35℃为183.78 U/mL。本研究还证实了椰壳基质固定化细胞的稳定性和可重复利用性,在6次循环利用后,固定化细胞的回收率为100% ~ 76.2%。最后,该研究确定了低成本、易于获得的基质和可重复利用的潜力,通过包埋在最佳条件下生产蛋白酶,用于细胞固定化技术。
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Alkaline Protease Production by Immobilized Klebsiella aerogenes Cells from Dairy Effluent Sludge
This study investigated the screening of alkaline protease microorganism from diary effluent sludge and identified by 16S ribosomal RNA nucleotide  sequence as Klebsiella aerogenes with accession number MF156964.1 and maximum identity 95.45%. The cells were immobilized with coconut pod husks  and optimization studies such as the effects of particle sizes, pH, temperature, agitation speed, and incubation time were determined. Out of  twenty three microorganisms screened, three were potential protease producers. K. aerogenes gave the highest zone of hydrolysis (35 mm) on the  skimmed milk agar plate. The particle size (0.075 mm2) of the immobilization agent gave the highest enzyme activity 176.83 U/mL. The optimum  incubation time for the production of protease was 48 h with enzyme activity 143.054 U/mL which further declined. The optimum pH of the protease was  pH 9.0 with activity 209.61 U/mL which made it alkaline. The agitation speed 150 rpm resulted in a protease activity 175.83 U/mL and reduced by 56.5% at  250 rpm. The optimal temperature 35 ºC was 183.78 U/mL. This study also confirmed the stability and reusability of the immobilized cells using the  coconut pod husks matrix by maintaining from 100% to 76.2% up to six times recycle. Conclusively, the study established the efficiency of low cost, readily  available matrix and reusability potentials of coconut pod husks for cells immobilization technology through entrapment at optimal conditions for  protease production. 
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