Zhang Yao, Xia Zhanfeng, Cao Xinbo, Li Jun, Zhang Lili
Key Laboratory of Protection and Utilization of Biological Resources in Tarim Basin of Xinjiang Production & Construction Corps, Tarim University, Alar 843300, China.
College of Life Science, Tarim University, Alar 843300, China.
Wei Sheng Wu Xue Bao. 2013 Aug 4;53(8):798-808.
We explored 4 new methods to improve the isolation of actinobacterial resources from high salt areas.
Optimized media based on 4 new strategies were used for isolating actinobacteria from hypersaline beaches. Glycerin-arginine, trehalose-creatine, glycerol-asparticacid, mannitol-casein, casein-mannitol, mannitol-alanine, chitosan-asparagineand GAUZE' No. 1 were used as basic media. New isolation strategy includes 4 methods: ten-fold dilution culture, simulation of the original environment, actinobacterial culture guided by uncultured molecular technology detected, and reference of actinobacterial media for brackish marine environment. The 16S rRNA genes of the isolates were amplified with bacterial universal primers. The results of 16S rRNA gene sequences were compared with sequences obtained from GenBank databases. We constructed phylogenetic tree with the neighbor-joining method.
No actinobacterial strains were isolated by 8 media of control group, while 403 strains were isolated by new strategies. The isolates by new methods were members of 14 genera (Streptomyces, Streptomonospora, Saccharomonospora, Plantactinospora, Nocardia, Amycolatopsis, Glycomyces, Micromonospora, Nocardiopsis, Isoptericola, Nonomuraea, Thermobifida, Actinopolyspora, Actinomadura) of 10 families in 8 suborders. The most abundant and diverse isolates were the two suborders of Streptomycineae (69.96%) and Streptosporangineaesuborder (9.68%) within the phylum Actinobacteria, including 9 potential novel species.
New isolation methods significantly improved the actinobacterial culturability of hypersaline areas, and obtained many potential novel species, which provided a new and more effective way to isolate actinobacteria resources in hypersaline environments.
我们探索了4种新方法以提高从高盐地区分离放线菌资源的效率。
基于4种新策略优化的培养基用于从高盐海滩分离放线菌。甘油-精氨酸、海藻糖-肌酸、甘油-天冬氨酸、甘露醇-酪蛋白、酪蛋白-甘露醇、甘露醇-丙氨酸、壳聚糖-天冬酰胺和GAUZE 1号培养基用作基础培养基。新的分离策略包括4种方法:十倍稀释培养、模拟原始环境、以未培养分子技术检测引导的放线菌培养以及参考适用于半咸水环境的放线菌培养基。用细菌通用引物扩增分离株的16S rRNA基因。将16S rRNA基因序列的结果与从GenBank数据库获得的序列进行比较。我们用邻接法构建系统发育树。
对照组的8种培养基未分离到放线菌菌株,而新策略分离到403株。新方法分离得到的菌株属于8个亚目中10个科的14个属(链霉菌属、链单孢菌属、糖单孢菌属、植放线孢菌属、诺卡氏菌属、拟无枝酸菌属、糖霉菌属、小单孢菌属、诺卡氏放线菌属、等节杆菌属、野野村菌属、嗜热栖热放线菌属、放线多孢菌属、马杜拉放线菌属)。放线菌门中最丰富和多样的分离株是链霉菌亚目(69.96%)和链孢囊菌亚目(9.68%)这两个亚目,包括9个潜在新物种。
新的分离方法显著提高了高盐地区放线菌的可培养性,并获得了许多潜在新物种,为在高盐环境中分离放线菌资源提供了一种新的、更有效的方法。