Isocitrate lyase,a new target in anti-tuberculosis drug research;
以异柠檬酸裂解酶为靶点筛选抗持留结核分枝杆菌药物
Differential expression of isocitrate lyase in P.marneffei phagocytized by nonstimulated and stimulated murine macrophages;
巨噬细胞内马尔尼菲青霉异柠檬酸裂解酶的表达
The relationship between expression of isocitrate lyase and development of penicillium marneffei yeast;
马尔尼菲青霉异柠檬酸裂解酶的表达与其酵母相生长的关系
With rice cultivating, sucrose was fed to the nutrient solution containing (NH_4)_2SO_4 (NH_4~+) or L-Ala, and then determined the activities of glutamine synthetase(GS), NADH-dependent glutamate synthase(NADH-GOGAT), phosphoenolpyruvate carboxylase(PEPC), NADP-dependent isocitrate dehydrogenase(NADP-ICDH), and NADH-dependent glutamate dehydrogenase(NADH-GDH).
将蔗糖分别加入到含有相同氮素浓度的(NH_4)_2SO_4(NH_4~+)或丙氨酸(Ala)作为氮源的营养液中培养水稻,测定幼苗根的谷氨酰胺合成酶(GS)、依赖于NADH的谷氨酸合酶(NADH-GOGAT)、磷酸烯醇式丙酮酸羧化酶(PEPC)、依赖于NADP的异柠檬酸脱氢酶(NADP-ICDH)和依赖于NADH的谷氨酸脱氢酶(NADH-GDH)的活性。
The activities of glutamine synthetase (GS) , NAD (H) -dependent glutamate dehydrogenase (NAD (H) -GDH), NADP-dependent isocitrate dehydrogenases (NADP-ICDH) ,the level of tatol soluble protein and soluble sugar were determined during germination and cotyledon development in Luffa cylindrical.
测定了不同培养条件下,丝瓜种子萌发及子叶发育时期子叶中谷氨酰胺合成酶(GS)、依赖于NAD(H)的谷氨酸脱氢酶(GDH)和依赖于NADP的异柠檬酸脱氢酶(ICDH)活性的变化,以及可溶性蛋白、总可溶性糖和其他参数的变化。
coli-Mycobacterium shuttle vector expressing Mycobacterium tuberculosis (MTB) latent infection related protein, isocitrate lyase (ICL) and green fluorescence protein (GFP) for future screening of drugs against the ICL expression and the latent infection of MTB.
coli 分枝杆菌穿梭载体 ,在耻垢分枝杆菌 (MS)中融合表达结核分枝杆菌(MTB)潜伏感染相关蛋白异柠檬酸裂合酶 (ICL)及绿色荧光蛋白 (GFP) ,为抗MTBICL的表达及抗MTB潜伏感染的药物筛选奠定基础 。
Isocitrate lyase (ICL) catalyses the first committed step of the glyoxylate bypass, which reversibly cleaves isocitrate into succinate and glyoxylate.
异柠檬酸裂合酶(Isocitrate lyase,ICL)在结核菌的潜伏期致病中起至关重要作用,是一个潜在的药物靶标。
With the method of starch gel electrophoresis,analysis of the patterns of IDH for introduction foreign DNA into soybean was conducted.
采用淀粉凝胶电泳的方法，对利用外源总ＤＮＡ导入栽培大豆的变异后代异柠檬酸脱氢酸（ＩＤＨ）酶谱进行了分析，结果表明：酶谱谱带清晰，呈现Ａ、Ｂ、Ｃ三种类型。