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通过圆柱假丝酵母的高细胞密度补料分批培养生产脂肪酶。

Production of lipase by high cell density fed-batch culture of Candida cylindracea.

作者信息

Kim Beom Soo, Hou Ching T

机构信息

Microbial Genomics and Bioprocessing Research Unit, National Center for Agricultural Utilization Research, Agricultural Research Service, United States Department of Agriculture, 1815 North University Street, Peoria, IL 61604, USA.

出版信息

Bioprocess Biosyst Eng. 2006 Jun;29(1):59-64. doi: 10.1007/s00449-006-0058-z. Epub 2006 Apr 1.

Abstract

Candida cylindracea NRRL Y-17506 was grown to produce extracellular lipase from oleic acid as a carbon source. Through flask cultures, it was found that the optimum initial oleic acid concentration for cell growth was 20 g l(-1). However, high initial concentrations of oleic acid up to 50 g l(-1) were not inhibitory. The highest extracellular lipase activity obtained in flask culture was 3.0 U ml(-1) after 48 h with 5 g l(-1) of initial oleic acid concentration. Fed-batch cultures (intermittent and stepwise feeding) were carried out to improve cell concentration and lipase activity. For the intermittent feeding fed-batch culture, the final cell concentration was 52 g l(-1) and the extracellular lipase activity was 6.3 U ml(-1) at 138.5 h. Stepwise feeding fed-batch cultures were carried out to simulate an exponential feeding and to investigate the effects of specific growth rate (0.02, 0.04 and 0.08 h(-1)) on cell growth and lipase production. The highest final cell concentration obtained was 90 g l(-1) when the set point of specific growth rate (mu(set)) was 0.02 h(-1). High specific growth rate (0.04 and 0.08 h(-1)) decreased extracellular lipase production in the later part of fed-batch cultures due to build-up of the oleic acid oversupplied. The highest extracellular lipase activity was 23.7 U ml(-1) when mu(set) was 0.02 h(-1), while the highest lipase productivity was 0.31 U ml(-1) h(-1) at mu(set) of 0.08 h(-1).

摘要

柱状假丝酵母NRRL Y - 17506以油酸作为碳源进行培养以产生胞外脂肪酶。通过摇瓶培养发现,细胞生长的最佳初始油酸浓度为20 g l(-1)。然而,高达50 g l(-1)的高初始油酸浓度并无抑制作用。在初始油酸浓度为5 g l(-1)的情况下,摇瓶培养48小时后获得的最高胞外脂肪酶活性为3.0 U ml(-1)。进行补料分批培养(间歇补料和逐步补料)以提高细胞浓度和脂肪酶活性。对于间歇补料分批培养,在138.5小时时最终细胞浓度为52 g l(-1),胞外脂肪酶活性为6.3 U ml(-1)。进行逐步补料分批培养以模拟指数补料,并研究比生长速率(0.02、0.04和0.08 h(-1))对细胞生长和脂肪酶产生的影响。当设定的比生长速率(μ(set))为0.02 h(-1)时,获得的最高最终细胞浓度为90 g l(-1)。由于过量供应的油酸积累,高比生长速率(0.04和0.08 h(-1))在补料分批培养后期降低了胞外脂肪酶的产生。当μ(set)为0.02 h(-1)时,最高胞外脂肪酶活性为23.7 U ml(-1),而在μ(set)为0.08 h(-1)时,最高脂肪酶生产率为0.31 U ml(-1) h(-1)。

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