首页> 外文期刊>Applied Biochemistry and Biotechnology >Effect of Aeration and Agitation Regimes on Lipase Production by Newly Isolated Rhodotorula mucilaginosa–MTCC 8737 in Stirred Tank Reactor Using Molasses as Sole Production Medium
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Effect of Aeration and Agitation Regimes on Lipase Production by Newly Isolated Rhodotorula mucilaginosa–MTCC 8737 in Stirred Tank Reactor Using Molasses as Sole Production Medium

机译:充气和搅拌方式对糖蜜为唯一生产介质的搅拌釜反应器中新分离的粘质红假单胞菌MTCC 8737产脂肪酶的影响

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The influence of media and process parameters (aeration and agitation) on fermentation broth rheology and biomass formation has been studied in 1.5-l stirred tank reactor for lipase production using Rhodotorula mucilaginosa MTCC 8737. Molasses, as sole production medium, is used for lipase production by varying aeration (1, 2, and 3 vvm) and agitation speeds (100, 200, and 300 rpm). Maximum lipase activity of 72 U/ml was obtained during 96 h of fermentation at 2 vvm, 200 rpm, pH 7, and 25 ± 2°C temperature. Lipase production kinetics with respect to dry cell weight of biomass showed Y P/S of 25.71 U/mg, specific product formation of 10.9 U/mg DC, and Y X/S 2.35 mg/mg. Maximum lipase activity (MC 2) of 56 U/ml was observed at 1% molasses, and a further increase in the molasses concentration of (%) 1.5 and 2 inhibited the product formation of lipase with 15 and 8.5 U/ml, respectively. The production kinetics of molasses media showed Y P/X was 14 U/mg DC, Y P/S 16 U/mg, and Y X/S 1.14 mg/mg during 96 h of bioreactor operation. The kLa values for all batches (MC 1–MC 4) at 96 h of fermentation were 32, 28, 21, and 19/h, and the |oxygen transfer rate were 54.4, 56, 35.7, and 17.29 mg/l h, respectively. Increase in molasses concentration resulted in decreased lipase activity by increase in viscosity of the fermentation broth.
机译:在1.5升搅拌罐反应器中,使用粘粒红球菌MTCC 8737生产脂肪酶,研究了培养基和工艺参数(通气和搅拌)对发酵液流变学和生物质形成的影响。糖蜜作为唯一的生产培养基,用于脂肪酶的生产通过改变曝气(1、2和3 vvm)和搅拌速度(100、200和300 rpm)。在2 vvm,200 rpm,pH 7和25±2°C温度下发酵96小时期间,最大脂肪酶活性为72 U / ml。相对于生物质干细胞重量的脂肪酶生产动力学表明,Y P / S 为25.71 U / mg,特定产物形成量为DC 10.9 U / mg,Y X / S 2.35 mg / mg。在1%糖蜜时观察到最大脂酶活性(MC 2)为56 U / ml,糖蜜浓度(%)1.5和2的进一步增加分别以15 U和8.5 U / ml抑制了脂肪酶的产物形成。在生物反应器96小时内,糖蜜培养基的生产动力学显示YP / X 为DC 14 U / mg DC,YP / S 16 U / mg和YX / S 1.14 mg / mg。操作。发酵96 h时所有批次(MC 1–MC 4)的kLa值分别为32、28、21和19 / h,氧的转移速率为54.4、56、35.7和17.29毫克/升·小时。糖蜜浓度的增加通过增加发酵液的粘度导致脂肪酶活性降低。

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