首页> 外文期刊>Journal of Microbiology, Biotechnology and Food Sciences >IMPROVEMENT OF PHYTASE BIOSYNTHESIS BY NEW BACTERIAL ISOLATE, PediococcuspentosaceusC4/1A VIA CONTINUOUS CULTIVATION
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IMPROVEMENT OF PHYTASE BIOSYNTHESIS BY NEW BACTERIAL ISOLATE, PediococcuspentosaceusC4/1A VIA CONTINUOUS CULTIVATION

机译:连续培养通过新细菌分离物PeodcoccuspentosaceusC4 / 1A改善植酸酶的生物合成

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Phytase producer was selected from five different lactic acid bacteria isolates obtained from the animal faeces sources from laboratory culture collection. From the five isolates, C4/1A showed the highest phytase activity (21.25 U/mL) as compared to others and was identified as PediococcuspentosaceusC4/1A by 16S rRNA gene sequencing. Optimization of medium formulation and culture conditions was conducted by a conventional method (one-factor-at-one-time) using response surface methodology(RSM). Effects of four parameters were studied on the bacterial growth, reducing sugar and phytase productions. The phytase biosynthesis increased from 21.2 U/mL to 42.3 U/mL using the optimized medium formulation and culture conditions. The RSM suggested that yeast extract, glucose, sodium phytate and inoculum size significantly improved by 99.2% production of phytase. Continuous cultivation was carried out at dilution rate ranging from 0.1 h-1 to 0.4 h-1 and the steady-state of P. pentosaceusC4/1A was achieved after five generations and three residence times. The cultivation was carried out for 48 h and the highest productivity of phytase and cell concentration was obtained at dilution rate 0.3 h-1 which resulted in 8.65 U/mL/h and 0.894 g/L/h, respectively. Throughout the cultivation process, production of phytase was improved by 89.3% from shake-flask experiment to 2L bioreactor.
机译:植酸酶生产者选自五个不同的乳酸菌分离株,这些分离株是从实验室培养物收集的动物粪便中获得的。在这五个分离物中,C4 / 1A的植酸酶活性最高(21.25 U / mL),与其他菌株相比,通过16S rRNA基因测序被鉴定为PediococcuspentosaceusC4 / 1A。培养基配方和培养条件的优化是使用响应面方法(RSM)通过常规方法(一次一因素)进行的。研究了四个参数对细菌生长,减少糖和植酸酶产量的影响。使用优化的培养基配方和培养条件,植酸酶的生物合成从21.2 U / mL增加到42.3 U / mL。 RSM指出,酵母提取物,葡萄糖,植酸钠和接种物的大小可显着提高植酸酶的99.2%产量。连续培养以0.1h-1至0.4h-1的稀释率进行,并且经过五代和三个停留时间后,戊糖假单胞菌C4 / 1A达到稳态。培养进行48小时,以0.3h-1的稀释率获得最高的植酸酶产量和细胞浓度,分别得到8.65U / mL / h和0.894g / L / h。在整个培养过程中,从摇瓶实验到2L生物反应器,植酸酶的产量提高了89.3%。

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