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作 者:陈艳红[1,2,3,4] 王海琪 马芮萍[1,2,3,4] 姜泽东 倪辉[1,2,3,4] 朱艳冰 CHEN Yanhong;WANG Haiqi;MA Ruiping;JIANG Zedong;NI Hui;ZHU Yanbing(College of Marine Food and Biological Engineering,Jimei University,Xiamen 361021,China;Fujian Provincial Key Laboratory of Food Microbiology and Enzyme Engineering,Xiamen 361021,China;Research Center of Food Biotechnology of Xiamen City,Xiamen 361021,China;Key Laboratory of Systemic Utilization and In-depth Processing of Economic Seaweed,Xiamen Southern Ocean Technology Center of China,Xiamen 361021,China)
机构地区:[1]集美大学海洋食品与生物工程学院,福建厦门361021 [2]福建省食品微生物与酶工程重点实验室,福建厦门361021 [3]厦门市食品生物工程技术研究中心,福建厦门361021 [4]厦门市南方海洋研究中心经济海藻资源化利用与深加工重点实验室,福建厦门361021
出 处:《集美大学学报(自然科学版)》2021年第3期206-213,共8页Journal of Jimei University:Natural Science
基 金:国家自然科学基金项目(41976124)。
摘 要:利用Plackett-Burman试验、最陡爬坡试验和响应面法,对培养基组成、培养条件对Stenotrophomonas sp.NTa发酵产琼胶酶的影响进行分析并优化,研究该菌株发酵产酶的动态规律,并利用薄层色谱和MALDI-TOF MS进行酶解产物的鉴定。结果显示,在琼脂、酵母浸膏、CaCl_(2)、MgSO_(4)·7H_(2)O、培养基的初始pH值、装液量、接种量几个因素中,酵母浸膏和培养基初始pH值对菌株NTa产琼胶酶具有显著影响,在含有1.03%酵母浸膏、初始pH=8.0的基础发酵培养基(NaCl、KNO_(3)、MgSO_(4)·7H_(2)O、CaCl_(2)、K_(2)HPO_(4)、FeSO_(4)·7H_(2)O、琼脂的质量浓度分别为50,5.0,5.0,0.2,0.1,0.02,2.0 g/L)中可获得最高的琼脂酶活力。菌株在28℃、180 r/min条件下发酵时,对数生长中后期快速合成琼胶酶。发酵48 h,琼胶酶活力高达2.688 U/mL。酶解72 h的产物分析结果显示,菌株NTa琼胶酶水解琼脂主要产生四糖。Effects of medium composition and culture conditions on agarase production by Stenotrophomonas sp.NTa in liquid culture were investigated by Plackett-Burman design,steepest ascent method and response surface methodology.The dynamic law of enzyme production by this strain was studied,and the enzyme hydrolytic products were analyzed by thin-layer chromatography and MALDI-TOF MS.Among the tested seven factors,including agar,yeast extract,MgSO_(4)·7H_(2)O,CaCl_(2),initial culture pH,liquid medium volume,and inoculum size,yeast extract and initial culture pH had significant effects on agarase production.The highest agarase production was obtained in the basic fermentation medium(NaCl 50.0 g/L,KNO_(3)5.0 g/L,MgSO_(4)·7H_(2)O 5.0 g/L,CaCl_(2)0.2 g/L,K_(2)HPO_(4)0.1 g/L,FeSO_(4)·7H_(2)O 0.02 g/L,agar 2.0 g/L)containing 1.03%yeast extract and with initial pH of 8.0.At the conditions of 25℃and 180 r/min,agarase was rapidly synthesized in the middle and late log phase during the fermentation.After incubation for 48 h,the agarase activity reached 2.688 U/mL.Analysis of the enzyme hydrolytic products after 72 h reaction showed that the hydrolysis of agar by strain NTa agarase mainly produced tetraose.
关 键 词:Stenotrophomonas sp. 响应面法 琼胶酶 优化 四糖
分 类 号:TS201.2[轻工技术与工程—食品科学]
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