首页 | 本学科首页   官方微博 | 高级检索  
     检索      

屠宰血液废弃物分解菌的筛选和鉴定
引用本文:陶志东,王致远,甘雨,马娜娜,马海锐,冉权,李富贵,马俊,丁功涛,铁文军,谢雕雕.屠宰血液废弃物分解菌的筛选和鉴定[J].农产品加工.学刊,2021(3).
作者姓名:陶志东  王致远  甘雨  马娜娜  马海锐  冉权  李富贵  马俊  丁功涛  铁文军  谢雕雕
作者单位:西北民族大学生命科学与工程学院;西北民族大学生物医学研究中心;临夏市俊林清真肉制品有限责任公司;甘肃绿能农业科技股份有限公司
基金项目:“科技助力经济2020”重点专项项目(SQ2020YFF0405583);中央高校基本科研业务费专项资金资助项目(31920190357)。
摘    要:筛选高效血液蛋白分解菌株,并进行鉴定和测定其微生物酶活,为进行屠宰血液废弃物的资源化利用提供试验材料。采用酪蛋白和哥伦比亚血琼脂平板培养基,以产生透明圈的比值大小作为判定的标准,从日喀则地区屠宰场的土壤中分离纯化出1株能高效降解蛋白质的菌株,编号为NwMCC01910045。在血琼脂平板培养基上,于37℃下培养24 h,通过福林酚法测得酶活力大小为88.69 U/mL。经生物学鉴定、生理生化测定和16S rRNA序列分析,并构建系统发育树,鉴定该菌株为吉氏库特菌(Kurthia sp.),是一株能有效降解血液蛋白的菌株。

关 键 词:菌株筛选  蛋白分解  血液蛋白

Screening and Identification of Slaughter Blood Waste Decomposing Bacteria
TAO Zhidong,WANG Zhiyuan,GAN Yu,MA Na'na,MA Hairui,Ran Quan,LI Fugui,MA Jun,DING Gongtao,TIE Wenjun,XIE Diaodiao.Screening and Identification of Slaughter Blood Waste Decomposing Bacteria[J].Nongchanpin Jlagong.Xuekan,2021(3).
Authors:TAO Zhidong  WANG Zhiyuan  GAN Yu  MA Na'na  MA Hairui  Ran Quan  LI Fugui  MA Jun  DING Gongtao  TIE Wenjun  XIE Diaodiao
Institution:(School of Life Science and Engineering,Northwest University for Nationalities,Lanzhou,Gansu 730000,China;Biomedical Research Center,Northwest University for Nationalities,Lanzhou,Gansu 730000,China;Linxia Junlin Halal Meat Products Co.,Ltd.,Linxia,Gansu 731100,China;Gansu Green Energy AgricultureTechnology Co.,Ltd.,Tianzhu,Gansu 733200,China)
Abstract:The purpose of this thesis was to screen high-efficiency blood proteolytic strains,and to identify and determine their microbial enzyme activities,so as to provide experimental materials for resource utilization of slaughter blood waste.In the experiment,casein and Columbia blood agar plate medium were used,and the ratio of the transparent circle was used as the criterion.A strain that can efficiently degrade protein was isolated and purified from the soil of the slaughterhouse in Xigaze area,numbered NwMCC01910045.After culturing on a blood agar plate medium at 37℃for 24 h,the enzyme activity was 88.69 U/mL as measured by the Folin method.After biological identification,physiological and biochemical determination and 16S rRNA sequence analysis,and constructing a phylogenetic tree,the strain was identified as Kurthia sp.,a strain that can effectively degrade blood proteins.
Keywords:strain screening  protein breakdown  blood protein
本文献已被 CNKI 维普 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号