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

一株菲降解菌的分离、鉴定及最佳培养条件的优化
引用本文:一株菲降解菌的分离、鉴定及最佳培养条件的优化.一株菲降解菌的分离、鉴定及最佳培养条件的优化[J].山东科学,2015,28(2):75-80.
作者姓名:一株菲降解菌的分离、鉴定及最佳培养条件的优化
作者单位:山东省科学院生物技术研究中心,山东省应用微生物重点实验室,山东 济南 250014
基金项目:山东省科学院先导科技专项(2013);国家高技术研究发展计划(863计划)(2013AA06A210);山东省科学技术发展计划(2014GSF117019)
摘    要:从石油污染场地分离到一株可降解菲的菌株SP 3,经生理生化鉴定和16S rDNA序列对比分析,初步鉴定该菌株为分枝杆菌(Mycobacterium sp.),该菌能够以菲为唯一碳源,在菲浓度为100 μg/mL的无机盐培养基中,28 ℃摇床培养7 d降解率达到了99%以上。对该菌进行了最佳发酵培养基及培养条件的优化研究,其最佳培养基配方为淀粉1%、牛肉膏1%、Na2HPO4 0.2%、NaH2PO4 0.2%,并通过单因素实验法确定了最佳培养条件为温度30 ℃,初始pH =7.5,培养时间12 h。

关 键 词:  多环芳烃  降解  培养基优化  
收稿时间:2014-07-23

Isolation,identification and optimization of growth conditions of a strain of phenanthrene degrading bacteria
HUANG Yu jie,QIU Wei zhong,GAO Yong chao,KONG Xue,ZHANG Wen,WANG Jia ning.Isolation,identification and optimization of growth conditions of a strain of phenanthrene degrading bacteria[J].Shandong Science,2015,28(2):75-80.
Authors:HUANG Yu jie  QIU Wei zhong  GAO Yong chao  KONG Xue  ZHANG Wen  WANG Jia ning
Institution:Shandong Provincial Key laboratory of Applied Microbiology, Biotechnology Center, Shandong Academy of Sciences, Jinan 250014,China
Abstract:A phenanthrene degradable strain SP 3 was isolated from petrol contaminated soil. It was roughly identified as Mycobacterium sp.through physiological and biochemical identification and contrast analysis of 16S rDNA sequences. Phenanthrene could be served as its unique carbon source.The degradation rate is more than 99% in such conditions as mineral salt medium of phenanthrene concentration of 100 μg/mL,shaking culture of 28 ℃ and 7 days. We discovered that optimal culture medium of strain SP 3 included starch of 1%, beef extract of 1%,Na2HPO4 of 0.2%and NaH2PO4 of 0.2%. We determined its optimum culture conditions of temperature of 30 ℃, initial pH of 7.5 and culture time of 12 h through single factor experiment.
Keywords:optimization of medium  degradation  phenanthrene  PAHs  
本文献已被 CNKI 万方数据 等数据库收录!
点击此处可从《山东科学》浏览原始摘要信息
点击此处可从《山东科学》下载免费的PDF全文
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