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首页> 外文期刊>Journal of Chemical Technology & Biotechnology >Optimization of medium and process parameters for a constitutive -amylase production from a catabolite derepressed Bacillus subtilis KCC103
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Optimization of medium and process parameters for a constitutive -amylase production from a catabolite derepressed Bacillus subtilis KCC103

机译:从分解代谢物抑制的枯草芽孢杆菌KCC103生产组成型淀粉酶的培养基和工艺参数的优化

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BACKGROUND: In Bacillus subtilis KCC103 -amylase is hyper-produced and not catabolite repressed by glucose. Various sugars, raw starches and nitrogen sources were tested for their repression effect on -amylase synthesis. Enhancement of -amylase production by supplementing micronutrients and surfactants was studied. Using optimized medium, process parameters were optimized for improved -amylase production. RESULTS: -Amylase was produced from KCC103 utilizing simple sugars indicating the absence of catabolite repression. Raw potato and yeast extract were best carbon and nitrogen sources for -amylase production. -Amylase synthesis was enhanced by micronutrients cysteine, thiamine, Mg2+ and SDS. Maximum -amylase (394 IU mL-1) was produced in the optimized medium consisting of (in g L-1) raw potato (30.0), yeast extract (20.0), cysteine (0.3), thiamine (0.2), SDS (0.2) and MgSO4 (0.5 mmol L-1) at 36-48 h under optimal conditions (pH 7.0, 37 °C, 200 rpm). The -amylase production was further enhanced to 537.7 IU mL-1 with shorter time (15-18 h) in a bioreactor with optimized agitation rate of 700 rpm at 30% dissolved oxygen. CONCLUSION: Since there was no carbon catabolite repression of -amylase synthesis, sugar mixture from various agro-residues hydrolysates could be utilized for -amylase production. The study showed the feasibility of utilization of raw potato for -amylase production from the KCC103, which would lead to a significant reduction in process cost.
机译:背景:在枯草芽孢杆菌中,KCC103-淀粉酶高产,且不被葡萄糖抑制。测试了各种糖,粗淀粉和氮源对淀粉酶合成的抑制作用。研究了通过补充微量营养素和表面活性剂来增强淀粉酶的生产。使用优化的培养基,对工艺参数进行了优化,以提高淀粉酶的产量。结果:-淀粉酶由KCC103利用简单的糖产生,表明不存在分解代谢物阻遏。生马铃薯和酵母提取物是淀粉酶生产的最佳碳源和氮源。 -微量营养素半胱氨酸,硫胺素,Mg2 +和SDS增强了淀粉酶的合成。在由(以L-1计)生马铃薯(30.0),酵母提取物(20.0),半胱氨酸(0.3),硫胺素(0.2),SDS(0.2)组成的优化培养基中产生了最大的淀粉酶(394 IU mL-1) )和MgSO4(0.5 mmol L-1)在最佳条件下(pH 7.0,37°C,200 rpm)在36-48小时内。在生物反应器中,在30%的溶解氧下,最佳搅拌速度为700 rpm,在较短的时间(15-18小时)内,α-淀粉酶的产量进一步提高至537.7 IU mL-1。结论:由于没有碳分解代谢物抑制α-淀粉酶的合成,各种农业残渣水解产物的糖混合物可用于α-淀粉酶的生产。研究表明,利用生马铃薯生产来自KCC103的淀粉酶的可行性,这将大大降低工艺成本。

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