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1)  engineered strain
工程菌株
1.
If the engineered strain Xhhh and informatics software (Ebis) were used, the specific degradation rate of Xhhh strain may be higher 128% than that of the natural bacterium XZ strain and the aeration tank needed may be 51% decreased.
如果应用工程菌株Xhhh和Ebis信息软件的双重优化技术 ,可使生物负荷效率提高1 2 8% ,所需曝气池体积可降低 5 1 % 。
2)  Agrobaterium tumefaciens
农杆菌工程菌株
1.
)/ Raphanus sativus -antifungal protein (R_S-AFP2) genes were constructed by gene engineering techniques and transferred into Agrobaterium tumefaciens EHA105 through direct transformation,they are GC+R/pCAMBIA1300/EHA105 and RC+G/pCAMBIA1300/EHA105.
、萝卜抗真菌蛋白 Raphanussativus-antifingalprotein,Rs-AFP2 的三价植物表达载体,并通过农杆菌直接转化法将三价植物表达载体转入农杆菌EHA105,分别为GC+R/pCAMBIA1300/EHA105和RC+G/pCAMBIA1300/EHA105,并采用PCR、DNAdotblotting技术对其进行了鉴定分析,证明获得了阳性的重组农杆菌工程菌株
3)  Cell engineering strains
细胞工程菌株
4)  Genetically Engineered Strains
遗传工程菌株
5)  genetically engineered microorganism m-CDS-1
基因工程菌株m-CDS-1
6)  industrial strain
工业菌株
1.
The plasmid containing XYL1 gene was transformed into the industrial strain of Saccharomyces cerevisiae 6508 and the G418 resistance gene KanMX acted as a dominant selectable marker.
将树干毕赤氏酵母(Pichia stipitis)木糖还原酶基因XYL1连接到适用于酿酒酵母工业菌株的多拷贝整合载体pYMIKP中,构建得到表达质粒pYMIKP-XYL1,转化酿酒酵母工业菌株Saccharomyces cerevisiae6508。
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