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中国生物工程杂志

China Biotechnology
China Biotechnology  2015, Vol. 35 Issue (8): 90-95    DOI: 10.13523/j.cb.20150813
    
Optimization of Fermentation Medium for Creatininase Production by Arthrobacter nicotiana
LIANG Jiang-guang, JIA Jia-hong, WU Jun-wei, ZHU Jie
School of Biology and Food Engineering, Changshu Institute of Technology, Changshu 215500, China
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Abstract  

The optimal culture medium of creatininase production on the Arthrobacter nicotiana were carried out. Firstly, using creatine as inductor and metal ions experiment, it was found that creatine and metal ions have a great influence upon the creatininase production. Secondly, single factor experiment showed the optimization carbon and nitrogen sources was soluble starch and corn steep liquor,but compound nitrogen source of yeast extract and corn steep liquor was much better(creatininase production reached 108.5 U/g wet mycelium). At last, creatininase production reached 182.5 U/g wet mycelium under the optimization of fermentation medium, which was about 19.87 times as high as the initial fermentation enzyme activity.



Key wordsArthrobacter nicotiana      Creatininase      Optimization of production medium     
Received: 23 March 2015      Published: 25 August 2015
ZTFLH:  Q93-335  
Cite this article:

LIANG Jiang-guang, JIA Jia-hong, WU Jun-wei, ZHU Jie . Optimization of Fermentation Medium for Creatininase Production by Arthrobacter nicotiana. China Biotechnology, 2015, 35(8): 90-95.

URL:

https://manu60.magtech.com.cn/biotech/10.13523/j.cb.20150813     OR     https://manu60.magtech.com.cn/biotech/Y2015/V35/I8/90


[1] 崔有宏, 罗侃, 郑强, 等. 肌酐测定工具酶产生菌烟草节杆菌02181的筛选及其产酶条件. 甘肃科学学报, 2005, 17(2): 49-53. Cui Y H, Luo K, Zheng Q, et al. Arthrobacter nicotianae 02181 which produces enzymes for diagnostic measurement of creatinine and its selected conditions for producing enzymes. Journa1 of GanSu Science, 2005, 17(2): 49-53.

[2] Yamamoto K, Oka M, Kikuchi T, et al. Cloning of the creatinine amidohydrolase gene from Pseudomonas sp PSJ. Biosci Biotech Biochem, 1995, 59(7): 1331-1332.

[3] Koyama Y, Yamamoto Otake, Suzuki M, et al. Cloning and expression of the sarcosine oxidase gene from Bacillussp S-19 in Escherichia coli. J Agric Biol Chem, 1991, 55(5): 1259-1263.

[4] 李萍,赵莹,余霆.肌酐在肾小球滤过功能损伤诊断中的价值的系统评价. 中国循证医学杂志,2004,4(11):752-758. Li P, Zhao Y,Yu T. Diagnostic value of creatinine for indicating glomerular filtration function injury: a systematic review. Chinese Journal of Evidence-based Medicine, 2004,4(11):752-758.

[5] 智强, 李淑慧, 高利宏, 等. 利用简并PCR克隆烟草节杆菌02181肌酸酶基因. 第三军医大学学报, 2007,29(12):1221-1223. Zhi Q,Li S H,Gao L H,et al. Gene cloning of creatinase from Arthrobacter nicotianae 02181 using degenerate PCR. Acta Academiae Medicinae Militaris Tertiae, 2007,29(12):1221-1223.

[6] 崔有宏, 罗侃, 郑强,等. 肌酐测定的酶学方法. 西北国防医学杂志, 2003, 24(2):129-131. Cui Y H, Luo K, Zheng Q, et al. Enzymatic method for the determination of creatinine. Medical Journal of National Defense Forces in Northwest China, 2003, 24(2):129-131.

[7] Paurekh A C, Cook S, Sims C, et al. A new method for the determination of serum creatinine based on reaction with 3,5-dinitrobenzoylchloride in an organic medium. Clin Chim Acta, 1976, 73(2): 221-231.

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