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作 者:杜敬河 王栩[1] 朱永安[1] 吴凤英 段杉[1,2]
机构地区:[1]华南农业大学食品学院,广东广州510642 [2]广东省天然活性物工程技术研究中心,广东广州510642 [3]广东永昊食品有限公司,广东阳江529536
出 处:《食品工业科技》2016年第13期157-161,共5页Science and Technology of Food Industry
基 金:广东省省部产学研合作专项资金项目(2013B090600111);广东省教育厅科研项目(2013gjhz0003)
摘 要:从土壤中分离得到一株产甲壳素酶的细菌,经形态学、生理生化及分子生物学鉴定,确定为多粘类芽孢杆菌,命名为A1。研究发现甲壳素、壳聚糖和淀粉可诱导该菌产甲壳素酶;添加尿素可提高甲壳素酶产量。本文研究确定该菌发酵产酶条件如下:培养基采用1%甲壳素(120目),0.05%Mg SO_4·7H_2O,1.2%尿素,0.5%Na Cl,0.07%K_2HPO_4,0.03%KH_2PO_4,0.3%酵母提取粉,初始p H4.5,接种龄12 h,接种量1%,于37℃培养78 h,在此条件下,该菌产甲壳素酶水平达到0.549 U/m L。该菌在对数期,其产酶曲线的上升略滞后于生长曲线变化;而在衰亡期,产酶曲线的降低略早于生长曲线的降低,说明该酶的mRNA的稳定性较差。A strain of chitinase producing bacteria was isolated from soil, and was identified to be Paenibacillus polymyxa based on its morphological, physiological and biochemical characteristics and I6S rDNA sequencing. The strain was named as Al.Chitin,chitosan and starch can induce A] to produce chitinase.The adding of urea in medium improved the production of chitinase.The fermentation conditions for chitinase production were determined as follows:the fermentation medium consisting of 1% chitin( 120 mesh),0.05% MgSQ-7H2O, 1.2% CO( NH2)2, 0.5% NaCI,O.03% KH2PO4 ,0.07% K2HPO4,0.3% yeast extract powder, pH4.5,starter culture age 12 h, inoculum size 1% ,fermenting at 37℃ for 78 h. Under such conditions, the chitinase activity achieved 0.549 U/mL. At the exponential phase,the rising of chitinase production curve slightly lagged behind the growth curve of A1, at the decline phase,the falling of chitinase production curve was slightly earlier than the falling of growth curve.The results indicated that the mRNA of the chitinase was unstable.
分 类 号:TS201.1[轻工技术与工程—食品科学]
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