葡萄糖脱氢酶
- 网络Glucose dehydrogenase;gdh;FAD-GDH;GDH-PQQ
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一株萤光假单孢杆菌(Pseudomonasfluorescens)中6-磷酸葡萄糖脱氢酶对烟酰胺核甙酸辅酶的专一性
The nicotinamide nucleotide specificity of glucose-6-phosphate dehydrogenase in a strain of Pseudomonas fluorescens
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6-磷酸葡萄糖脱氢酶(glucose-6-phosphateDehydrogenase,G6PDH)起到主要的再生NADPH的作用,其酶活随着氧限制程度的提高不断降低。
The enzyme of glucose-6-phosphate dehydrogenase ( G6PDH ) played a major role in NADPH regeneration and its activity decreased remarkably with the increase of oxygen limitation . 3 .
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UDP-葡萄糖脱氢酶(HasB)是透明质酸合成中的一个关键酶,而C类链球菌的UDP-葡萄糖脱氢酶编码基因(hasB)尚未被克隆。
The hasB of group C Streptococci has not been cloned and characterized . The putative UDP-glucose dehydrogenase gene ( hasB ) was cloned and sequenced .
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以甲苯胺兰(TB)修饰碳糊微电极为基体,将葡萄糖脱氢酶(GDH)用丝素蛋白膜固定于修饰微电极表面制成了生物传感器。
An amperometric glucose dehydrogenase biosensor is reported . It is made up of toluidine blue ( TB ) modified carbon paste microelectrode and enzyme film by glucose dehyrogenase immobilized on silk fibroin .
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在所检的遗传位点中,以D血型、运铁蛋白(Tf)、蛋白酶抑制剂(Pi)和6-磷酸葡萄糖脱氢酶(6-PGD)检测亲仔关系错误的效果最好;
In all 16 systems , the D blood group , transferrin ( Tf ), protease inhibitor ( Pi ) and 6-phosphogluconate dehydrogenase ( 6-PGD ) were the most effective loci for detection of parentage errors .
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盐藻多糖合成关键酶&尿苷二磷酸葡萄糖脱氢酶(DsUGD)基因分析及耐盐相关性研究
Sequence Analysis and Salinity Stress Studies about UDP-glucose Dehydrogenase of Dunaliella Salina ( DsUGD ) - a Key Enzyme in the Polysaccharide Metabolism
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磷酸葡萄糖脱氢酶、乙醇脱氢酶催化和3-异戊基苹果酸脱氢酶在盐处理的耐盐番茄根系中显著增加,异戊烯二磷酸(IDP)异构酶显著减少。
Alcohol dehydrogenase , Phosphogluconate dehydrogenase and 3-Isopropylmalate dehydrogenase were up-regulated proteins in salt-tolerant tomato under salinity , while the only identified protein in salt tolerant plants was the isopentenyl diphosphate ( IDP ) isomerase .
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本实验室首次从盐藻中克隆得到尿苷二磷酸葡萄糖脱氢酶DsUGD基因,并发现高盐胁迫对DsUGD基因具有明显的诱导作用。
In our laboratory , we have first cloned this gene from Dunaliella salina ( DsUGD ), and found that the high salinity can induce the expression .
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研究在变温条件下GA3对辽东楤木种子解除休眠过程和呼吸代谢途径关键酶(磷酸己糖异构酶、6-磷酸葡萄糖脱氢酶、6-磷酸葡萄糖酸脱氢酶、琥珀酸脱氢酶)的活性变化。
This study investigated the change 6-phosphogluconate dehydrogenase and succinic dehydrogenase and in the contents of metabolic substances in the activity of key enzymes for respiratory metabolic pathway hexosephosphate isomerase , 6-zwischenferment , in the Japanese aralia ( Aralia elata ) seed dormancy-breaking process under alternating temperature .
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异丙肾上腺素对大鼠肝细胞氮代谢及6-磷酸葡萄糖脱氢酶活性的影响
Effects of isoproterenol on nitrogen metabolism and G6PDH activity of rat hepatocyte
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并且确定了D-葡萄糖脱氢酶活力可以作为选育指标,进行D-核糖生产菌株的选育。
The D-ribose-producing bacterium was obtained according on its D-dehydrogenase .
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葡萄糖脱氢酶法测定血清葡萄糖的方法学评价
Evaluation of glucose dehydrogenase method for determination of serum glucose
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红细胞6-磷酸葡萄糖脱氢酶缺乏者的白细胞活酶
Leukocyte Enzyme Activity in Erythrocyte Glucose - 6 - Phosphate Dehydrogenase Deficiency
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人乳腺癌组织中6-磷酸葡萄糖脱氢酶活性及同工酶的分析
Determination of Activity of Glucose-6-Phosphate Dehydrogenase and Its Isoenzymes in Human Breast Carcinoma
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巨大芽孢杆菌葡萄糖脱氢酶基因的重组和表达研究
Recombination and expression of glucose dehydrogenase from Bacillus megaterium
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葡萄糖脱氢酶连续监测法的研究
Study on the Continuous Monitoring Assay of Glucose Dehydrogenase
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尿苷二磷酸葡萄糖脱氢酶的基因克隆及在原核细胞中的表达
The cloning of uridine diphosphate glucose dehydrogenase gene and its expression in Escherichia coli
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结论:葡萄糖脱氢酶法是临床测定血清葡萄糖的较理想的方法。
Conclusion : Glucose dehydrogenase method was a perfect way for determination of serum glucose .
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丙酮酸氧化酶的缺陷同时也导致了6-磷酸葡萄糖脱氢酶和乙酰辅酶A合成酶活力的升高。
The pyruvate oxidase mutation also resulted in the activation of glucose-6-phosphate dehydrogenase and acetyl-CoA synthetase .
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这些结果表明所克隆的基因是兽疫链球菌的UDP-葡萄糖脱氢酶编码基因。
These data demonstrated that hasB encodes the UDP - glucose dehydrogenase of group C Streptococci .
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目的:通过方法学试验对葡萄糖脱氢酶法测定血清葡萄糖方法进行评价。
Objective : Glucose dehydrogenase ( GDH ) method for determination of serum glucose was evaluated through methodology test .
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伴随着种子的发育进程,6-磷酸葡萄糖脱氢酶、异柠檬酸裂解酶、异柠檬酸脱氢酶和琥珀酸脱氢酶的活性均有不同程度的增强。
There were gradually increased in activities of glucose-6-phosphate dehydrogenase , isocitrate lyase , isocitrate dehydrogenase and succinate dehydrogenase .
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对本地区的孕妇及其丈夫应常规检查,如疑有红细胞6-磷酸葡萄糖脱氢酶缺陷,其新生儿预防性服药可减轻高胆程度;
Doubted with glucose-6-phosphate dehydrogenase deficiency , the new-borns should preventively take some medicine to reduce the level of hyperbilirubinema .
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利用改造的对6-磷酸葡萄糖脱氢酶的硝基四氮唑蓝定性法对提取的细胞间隙液进行鉴定,结果显示得到了比较纯的细胞间隙液。
Using the tetrazolium-linked cytochemical method for estimation of glucose-6-phosphate dehydrogenase activity , the result indicate that extracted intercellular washing fluids is more pure .
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结果表明二年生健康针叶的6-磷酸葡萄糖脱氢酶的活性水平与针叶的抗病性有密切关系。
The results showed that there were close relations between the activity levels of glucose-6-phosphate dehydrogenase and disease resistance in two-year-old needles of slash pine .
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采用淀粉凝胶电脉及琼脂覆盖技术对三河马血液红细胞6-磷酸葡萄糖脱氢酶和葡萄糖磷酸异构入酶的电泳变异进行了检测。
Red cell 6-phosphogluconate dehydrogenase ( 6-PGD ) and glucosephosphate isomerase ( GPI ) in Sanhe horses were detected in starch gels using agar overlay technique .
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在油分旺盛合成期,6-磷酸葡萄糖脱氢酶和异柠檬酸裂解酶的活性均达到了最大值,而此时,异柠檬酸脱氢酶和琥珀酸脱氢酶的活性均增加较慢;
The activities of glucose-6-phosphate dehydrogenase and isocitrate lyase increased to maximum , however , the activities of isocitrate dehydrogenase and succinate dehydrogenase increased slowly when oil synthesized rapidly .
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用淀粉凝胶电泳及琼脂覆盖技术对山丹马的血液红细胞6磷酸葡萄糖脱氢酶和葡萄糖磷酸异构酶的电泳变异进行了测定。
Red cell 6 Phosphogluconate dehydrogenase ( 6 PGD ) and glucose phosphate isomerase ( GPI ) in Shandan horses were studied by use of starch gels with using agar overlay technique .
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苹果酸脱氢酶、苹果酸酶、异柠檬酸脱氢酶、琥珀酸脱氢酶、醇脱氢酶、乳酸脱氢酶、6-磷酸葡萄糖脱氢酶和三磷酸腺苷激酶是与能量代谢相关的酶。
Malate dehydrogenase , malic enzyme , isocitrate dehydrogenase , succinate dehydrogenase , alcohol dehydrogenase , lactate dehydrogenase , 6-phosphogluconate dehydrogenase ( G-6-PDH ) and adenosine triphosphatase ( ATPase ) are isozymes related with energy metabolism .
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这些酶中叶子细胞的6-磷酸葡萄糖脱氢酶和超氧化物歧化酶的酶量都与蔗糖含量高度相关,在根细胞中与蔗糖含量高度相关的是过氧化物酶和苹果酸脱氢酶。
In these enzymes of the leaf cell , the quantity of 6 - GDP and the SOD were highly increased that is connected with the sucrose content , and what was related with the sucrose content in the root cell were the POD and the MDH .