介绍含重金属抗性基因工程菌的构建；
The construction of genetically engineered metal-resistance strain is introduced.
方法构建基因工程菌，利用甲醇诱导表达。
MethodThe genetic engineering bacteria was constructed, and induced by methanol.
外源基因在该基因工程菌中得到了高效表达。
The gene was highly expressed in the engineering bacterial strain.
目的建立重组NK4融合基因工程菌的发酵工艺。
Objective To develop a fermentation procedure for recombinant E. coli strain expressing NK4 gene.
他的公司将提供酶和生产完全替代型燃料所需要的基因工程菌。
He will provide the enzymes and genetically engineered bacteria needed to make a drop-in fuel.
利用基因工程菌消氮细菌及沉淀细菌对实验水体进行生物修复。
Utilize fungus uses genetic engineering such as the nitrition and sedemlate to carry on the bioremediation to repair to the experiment water.
项目目标：开发利用二氧化碳、氧气和氢气合成丁醇的基因工程菌；
Project Goals: Develop genetically modified bacteria that use carbon dioxide, oxygen and hydrogen to produce butanol.
对植酸酶基因工程菌（E-22）发酵产植酸酶条件作了初步研究。
The fermenting processes of the genic engineering strain E-22 for producing phytase were studied.
目的：优化融合表达抑肽酶基因工程菌的发酵条件，分离纯化抑肽酶。
Aim: to optimize the fermentation conditions of engineering bacteria expressing fusion proteins composed of aprotinin and to purify aprotinin.
利用含重金属抗性基因工程菌处理含重金属废水具有广阔的应用前景。
Application of genetically engineered metal-resistance strain for treating wastewater containing heavy metal appears to be a potential and effective approach.
项目目标：构建一种以电能代替太阳能生产高辛烷含量汽油的基因工程菌。
Project Goal: Genetically engineer micro-organisms to use electricity instead of sunlight to make a high-octane gasoline substitute.
通过转化绿色荧光蛋白基因质粒，对阿特拉津降解基因工程菌进行标记。
The atrazine-degrading genetically engineered microorganism(GEM) was labeled by transforming a plasmid containing green fluorescent protein(GFP) gene.
构建高活性la异构酶的基因工程菌是实现生物酶异构法产业化的重要前提。
Constructing gene engineering strains which produce high activity LA isomerase was an important presupposition for realizing industrialization with bio-enzymes methods.
目的构建生产辅酶Q 10的大肠杆菌基因工程菌并研究相关酶的表达情况。
OBJECTIVE To construct Escherichia coli producing coenzyme Q10 and investigate the decaprenyl diphosphate synthase expression.
本研究利用分子生物学技术构建高效的镍富集基因工程菌，并用于含镍废水的处理。
The effective nickel sorption genetic engineered strain was constructed using molecular biology technique and was applied to nickel-containing Wastewater treatment in this research.
本发明涉及一种基因工程菌，以及该基因工程菌的制备方法及其用途，属于生物工程技术领域。
The present invention relates to a gene engineered bacteria, and its preparation method and USES, belongs to biological engineering field.
目的：优化重组铜绿假单胞菌外毒素A（PEA）基因工程菌的发酵条件，实现PEA的高效表达。
Objective:To optimize the fermentable conditions of recombinant E. coli BL21 for high level expression of PEA.
为构建高产1，3-丙二醇或利用葡萄糖为底物产1，3-丙二醇克雷伯氏基因工程菌打下基 础。
The method lays a solid foundation for the high yield of 1,3- PDO or the yield of 1,3- PDO klebsiella gene engineering with glucose as a substrate.
根据基因工程菌高密度发酵过程中对P H值控制的要求，采用模糊控制实现基因工程菌高密度发酵罐的PH值控制。
Basing on the need of PH control in process of engineering bacteria highly dense fementation, fuzzy control completes the task of the PH control of engineering bacteria highly dense fementation.
测定了猪生长激素基因工程菌不同表达效率时细菌总蛋白的含量以及包涵体中重组猪生长激素占包涵体总蛋白的比值。
We determined the content of the total bacterial proteins and the proportion of recombinant porcine growth hormone(rpGH)in inclusion bodies(IBs)in the cultures of genetically engineered rpGH E.
正在应用的或处于研究阶段的构建瘤胃基因工程菌的方式主要有基因缺失技术、基因复制性重组技术和启动子的应用技术。
The main methods used, or under investigation, for production of rumen gene engineering bacteria are:gene deletion technique, gene recombination technique and the application of promotor.
对以淀粉和纤维素为原料的发酵制燃料酒精技术进行了比较，对木糖基因工程菌的构建及发酵工艺的国外新进展进行了讨论。
Different raw materials including cellulose and starch for ethanol fermentation are compared, and some new methods, for instance, recombinant xylose microorganisms are also discussed.
本实验室通过基因工程已构建了一株植酸酶高产基因工程菌e - 22，其遗传稳定性及酶学性质等均能很好的满足生产需要。
Our laboratory has constructed a genetic engineering phytase strain E-22. Its hereditary stability and enzyme character can well meet production's need.
这使得人们可利用基因工程技术来构建工程菌，增加有效组分的产出和生产新型的阿维菌素。
According to the cloned gene cluster, people can use genetical technology to obtain the genetical strains which can produce more potent and non-toxical avermectins and its derivatives.
目的：利用基因工程技术，构建表达具溶栓活性的纳豆激酶的大肠杆菌工程菌。
AIM: to construct engineered E. coli strains which can express nattokinase with fibrinolysis activity using gene engineering technology.
目的：利用基因工程技术，构建表达具溶栓活性的纳豆激酶的大肠杆菌工程菌。
AIM: to construct engineered E. coli strains which can express nattokinase with fibrinolysis activity using gene engineering technology.
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