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黑曲霉NCIM 563在深层发酵条件下植酸酶生产的菌株改良及放大培养

Strain improvement and up scaling of phytase production by Aspergillus niger NCIM 563 under submerged fermentation conditions.

作者信息

Shah P, Bhavsar K, Soni S K, Khire Jayant Malhar

机构信息

NCIM Resource Center, National Chemical Laboratory, Pune, 411 008, India.

出版信息

J Ind Microbiol Biotechnol. 2009 Mar;36(3):373-80. doi: 10.1007/s10295-008-0506-7. Epub 2008 Dec 10.

DOI:10.1007/s10295-008-0506-7
PMID:19082644
Abstract

Combination of physical and chemical mutagenesis was used to isolate hyper secretory strains of Aspergillus niger NCIM 563 for phytase production. Phytase activity of mutant N-1 and N-79 was about 17 and 47% higher than the parent strain. In shake flask the productivity of phytase in parent, mutant N-1 and N-79 was 6,181, 7,619 and 9,523 IU/L per day, respectively. Up scaling of the fermentation from shake flask to 3 and 14 L New Brunswick fermenter was studied. After optimizing various fermentation parameters like aeration, agitation and carbon source in fermentation medium the fermentation time to achieve highest phytase activity was reduced considerably from 14 days in shake flask to 8 days in 14 L fermenter. Highest phytase activity of 80 IU/ml was obtained in 1% rice bran-3.5% glucose containing medium with aeration 0.2 vvm and agitation 550 rpm at room temperature on 8th day of fermentation. Addition of either bavistin (0.1%), penicillin (0.1%), formalin (0.2%) and sodium chloride (10%) in fermented broth were effective in retaining 100% phytase activity for 8 days at room temperature while these reagents along with methanol (50%) and ethanol (50%) confer 100% stability of phytase activity at 4 degrees C till 20 days. Among various carriers used for application of phytase in feed, wheat bran and rice bran were superior to silica and calcium carbonate. Thermo stabilization studies indicate 100% protection of phytase activity in presence of 12% skim milk at 70 degrees C, which will be useful for its spray drying.

摘要

采用物理诱变和化学诱变相结合的方法,筛选出黑曲霉NCIM 563的高产植酸酶分泌菌株。突变株N-1和N-79的植酸酶活性比亲本菌株分别高出约17%和47%。在摇瓶中,亲本、突变株N-1和N-79的植酸酶产量分别为每天6181、7619和9523 IU/L。研究了从摇瓶发酵扩大到3 L和14 L新不伦瑞克发酵罐的发酵过程。优化了发酵培养基中的通气、搅拌和碳源等各种发酵参数后,达到最高植酸酶活性的发酵时间从摇瓶中的14天大幅缩短至14 L发酵罐中的8天。在发酵第8天,于室温下,在含1%米糠-3.5%葡萄糖的培养基中,通气量0.2 vvm,搅拌速度550 rpm,可获得最高80 IU/ml的植酸酶活性。在发酵液中添加0.1%的多菌灵、0.1%的青霉素、0.2%的福尔马林和10%的氯化钠,可使植酸酶活性在室温下8天内保持100%;而这些试剂与50%的甲醇和50%的乙醇一起,可使植酸酶活性在4℃下稳定20天。在用于饲料中植酸酶应用的各种载体中,麦麸和米糠优于二氧化硅和碳酸钙。热稳定性研究表明,在70℃下,12%的脱脂乳可100%保护植酸酶活性,这对其喷雾干燥很有用。

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