2) Luminescent engineered rhizobia
发光工程根瘤菌
3) gene engineering strain
基因工程菌
1.
Decoloration of azo dye wastewater by an anaerobic membrane bioreactor using gene engineering strain Escherichia coli JM109 (pGEX-AZR);
基因工程菌在厌氧膜生物反应器中对偶氮染料废水的脱色
2.
A L-serine gene engineering strain Brevibacterium flavm C-11A was investigated by the flask-shaking fermentation investigated research to determine the mycelium activation way and the flask-shaking fermentation condition through the single factor.
以基因工程菌株Brevibacterium flavmC-11A为L-丝氨酸产生菌,研究L-丝氨酸的摇瓶发酵条件,确定了菌体活化方式,并通过单因素确定了摇瓶发酵条件为:酵母膏浓度为14 g/L,缓冲剂为KH2PO4,碳氮比为10∶3。
3.
L-sorbose/L-sorbosone dehydrogenase produced by gene engineering strain Y517# can transform L-sorbose to 2-KGA, the Vitamin C precursor.
基因工程菌Y517#能表达醇醛脱氢酶,将L-山梨糖转化为VC的前体2-酮基-古龙酸(2-KGA)。
4) genetic engineering bacteria
基因工程菌
1.
The movement and its mechanism of genetic engineering bacteria in soils by non-uniform electric field.;
非均匀电场对土壤中基因工程菌的迁移与机理
2.
Construction of genetic engineering bacteria for recombinant human cardiac troponin Ⅰ;
重组人心肌肌钙蛋白Ⅰ基因工程菌的构建
3.
Fermentation of genetic engineering bacteria of insulin-like growth factor-Ⅰ;
重组胰岛素样生长因子-Ⅰ基因工程菌的发酵研究
5) genetically engineered strain
基因工程菌
1.
The Decoloration on Azo Dye in a Membrane Bioreactor by Genetically Engineered Strain;
基因工程菌在膜生物反应器中对偶氮染料的脱色
2.
Decoloration and bioaugmentation on azo dye are investigated by using immobilized genetically engineered strain Escherichia coli JM109(pGEX-AZR) on marcroporous foam carriers.
利用聚亚胺酯大孔泡沫吸附固定基因工程菌Escherichia coliJM109(pGEX-AZR),研究其对偶氮染料的脱色动力学及生物强化作用。
3.
Treating this sort of wastewater with genetically engineered strains instead of general microorganism can lead to high applicability and treatment efficiency.
介绍了基因工程菌的构建方法及其在重金属及难降解废水中的应用现状,探讨了处理过程中的影响因素,并简要阐述了在构建和应用菌种中所存在的问题。
6) Genetic engineering strain
基因工程菌
1.
Progress of asymmetric reduction of chiral alcohol with genetic engineering strain;
基因工程菌在不对称还原制备手性醇中的应用进展
2.
High cell density fermentation conditions of nattokinase by genetic engineering strain Pichia pastoris GS115/pPRONK1
毕赤酵母基因工程菌高密度发酵产纳豆激酶条件研究
3.
Using pET22b(+) as the expressing vector,the genetic engineering strain BL21-pET22b(+)-argE producing acetylornithine deacetylase was successfully constructed,and the genetic stability of the strain was studied.
利用质粒pET22b(+)为表达载体,成功构建了产N-乙酰鸟氨酸脱乙酰基酶基因工程菌BL21-pET22b(+)-argE,并考察了重组质粒的稳定性。
补充资料：根瘤菌入侵豆科植物根形成的根瘤
[图]
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条