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

黑暗链霉菌与卡那链霉菌原生质体融合研究
引用本文:程骥,洪文荣,苏建章,叶荔榕.黑暗链霉菌与卡那链霉菌原生质体融合研究[J].福州大学学报(自然科学版),2003,31(1):111-115.
作者姓名:程骥  洪文荣  苏建章  叶荔榕
作者单位:1. 福州大学侨兴轻工学院,福建,福州,350002
2. 福州抗生素总厂,福建,福州,350002
摘    要:进行了黑暗链霉菌与卡那链霉菌原生质体融合实验 .结果表明 ,将孢子悬浮液接种于种子培养基 ,然后转移到含 0 .5 %Gly的菌丝体培养基收获的菌丝体对形成原生质体最有利 .分别采用 10mg mL、6 0min及 5mg mL、75min的溶菌酶浓度与酶解时间制备黑暗链霉菌与卡那链霉菌原生质体能达到较高的形成率和再生率 .采用单亲灭活卡那链霉菌原生质体的种间融合法 ,得到与亲株形态明显不同的杂合体菌落 ,并筛选到44株妥布霉素产率提高的菌株 ,幅度最高达到 39% .

关 键 词:黑暗链霉菌  卡那链霉菌  妥布霉素  卡那霉素  原生质体融合
文章编号:1000-2243(2003)01-0111-05
修稿时间:2002年8月23日

Study on protoplast fusion between Streptomyces tenebrarius and Streptomyces kanamyceticus
CHENG Ji,HONG Wen-rong,SU Jian-zhang,YE Li-rong.Study on protoplast fusion between Streptomyces tenebrarius and Streptomyces kanamyceticus[J].Journal of Fuzhou University(Natural Science Edition),2003,31(1):111-115.
Authors:CHENG Ji  HONG Wen-rong  SU Jian-zhang  YE Li-rong
Institution:CHENG Ji1,HONG Wen-rong1,SU Jian-zhang1,YE Li-rong2
Abstract:The protoplast fusion between Streptomyces tenebrarius and Streptomyces kanamyceticus was studied. The spores were cultivated in seed media firstly for 24?h, then transferred into mycelia media with 0.5%Gly and cultivated further for 24?h, that high quantity and quality mycelia which were easy to prepare protoplasts can be gotten. The experiment showed that high qulity S.tene protoplasts can be gained in 10?mg/mL lysozyme for 60?min and high qulity S.kana protoplasts can be gained in 5?mg/mL lysozyme for 75?min. By inactivating S.kana protoplasts and then fusing the two kinds protoplasts, there were three kinds recombinants colonies which were quite different in size, color and morphorlogy can be observed in plate.From these different colony, 44 positive recombinants were selected of which the highest tobramycin potency increased 39% than that of the parent strain.
Keywords:Streptomyces tenebrarius  Streptomyces kanamyceticus  tobramycin  kanamycin  protoplasts fusion
本文献已被 CNKI 万方数据 等数据库收录!
点击此处可从《福州大学学报(自然科学版)》浏览原始摘要信息
点击此处可从《福州大学学报(自然科学版)》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