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磷酸化酶

与 磷酸化酶 相关的网络例句 [注:此内容来源于网络,仅供参考]

In the leaves, the mesophyll cells surrounding the vascular bundles contain the carbon dioxide-fixing enzyme phosphoenolpyruvate carboxylase in their cytoplasm.

在叶片中,叶肉细胞包围着维管束,叶肉细胞细胞质中所包含的磷酸烯醇式丙酮酸羧化酶,具有比核酮糖二磷酸羧化酶更高的的与二氧化碳的亲和力。

Thus, it is important to enucleate the catalytic centre and mechanism of transferrins as a phosphatase, which may have a potential significant in the protein phosphorylation process.

据文献报导,传铁蛋白家族中的某些乳传铁蛋白和铁结合蛋白具有磷酸酶的功能,因此,研究传铁蛋白磷酸酶学功能位点和作用机制并进一步确定它们在磷酸化过程的作用具有重要意义。

In search of databases, the deduced products of sanP, sanQ, sanR, sanS, sanT and sanU show highest similarity to those of nikP2, nikQ, nikR, nikS, nikT and nikU of S. tendae respectively. In comparison with the proteins of identified function, it is indicated that sanP encodes a thioesterase, sanQ encodes a cytochrome P450, sanR encodes a uracil phosphoribosyltransferase, sanS encodes a carboxylase, sanT encodes a histidinol-phosphate aminotransferase and sanU encodes a mutase.

在蛋白数据库中比较结果表明,sanP、sanQ、sanR、sanS、sanT和sanU基因编码的蛋白分别和唐德链霉菌的尼可霉素生物合成基因nikP2、nikQ、nikR、nikS、nikT、nikU六个基因编码的蛋白同源性最高;根据和已知功能蛋白的比较,推测sanP基因编码的是硫酯酶,sanQ基因编码的是细胞色素P450,sanR基因编码的是尿嘧啶磷酸核糖转移酶,sanS基因编码的是羧化酶,sanT基因编码的是组氨醇磷酸氨基转移酶,sanU基因编码的是一种变位酶。

Results showed that yield of TCA-N in phosphorylated fish protein hydrolysate approached to that of the control sample and phosphatization had little effect on hydrolysis.

对低值鱼蛋白磷酸化改性,并进行体外酶解,研究了磷酸化鱼蛋白的酶解特性(酶解物氨态氮得率、TCA可溶性肽得率及肽分子量分布)。

And also Hill reaction activity, unicycle photosynthetic phosphorylation activity and ATPase activity of flag leaves were positively correlated with photosynthetic rate.

而。且希尔反应活力、光合磷酸化活力及ATP酶活力与光合速率呈显著的正相关,因此希尔反应活力、光合磷酸化活力及ATP酶活力均可以作为高光效的的生理指标。

Ribulose bisphotosphate carboxylase (RuBP carboxylase ; rubisco) An enzyme that catalyzes the carboxylation of ribulose biphosphate to two molecules of glycerate 3-phosphate, the carbon dioxide-fixing first step in the Calvin cycle of PHOTOSYNTHESIS.

1,5-二磷酸核酮糖羧化酶:催化核酮糖-1,5-二磷酸成为两分子3-磷酸甘油酸的酶,这是光合作用卡尔文循环中,二氧化碳固定的第一位反应。

A diverse range of effects:on protein solubility and secretion was observed,and these effects were highly dependent on the particular chaperone.In the host strain over-expressing chaperone SecB harboroing pSecB,the amount of total periplasmic proteins was increased by about 71%and the activities of alkaline phosphatseand GL-7-ACA acylase(GL7A)were increased by about 54%and l.5-fold respectively.In the host strain over-expressing chaperone GroEL bearing pGroEL,the amount of total periplasmic proteins was increased by 52%,and the activity of penicillin G acylasewas in creased by about 76%;about 90%of Hexameric Calcitonin(Cal6)inclusion body and l5%of MS2interleukin3(MS2-HIL3)inclusion body became soluble respectively.All the data were compared with the parental strains un-bearing plasmdis pSecB or pGroEL.

在过量表达SecB的宿主菌中,周质空间分泌蛋白总量较对照组提高了约71%,GL-7-ACA酰化酶在周质空间酶的活力较对照组提高了约1.5倍,碱性磷酸酯酶在周质空间酶的活力较对照组提高了约54%;在过量表达GroEL的宿主菌中,周质分泌蛋白总量较对照组提高了约52%,青霉素G酰化在周质空间酶的活力较对照组提高了约76%,鲑鱼降钙素六聚体的可落性组分的比例由原来的45%增加到约90%,而MS2-人白介素-3融合蛋白的包涵体有约15%转变为可溶性组份。

These changes were prevented by genistein (a protein tyrosine kinase inhibitor) and antioxidant N-acetyl-L-cysteine, but promoted by sodium orthovanadate (a protein phosphatase inhibitor), which were administered to the SD rats 20 min before ischemia.

进一步的研究表明,缺血前20 min腹腔注射给药,然后缺血30 min,发现蛋白酪氨酸激酶抑制剂染料木黄酮和抗氧化剂N-乙酰半胱氨酸能显著地抑制核内STAT3的磷酸化水平及DNA结合活性的增加(磷酸化水平从2.3和2.5倍分别降为1.2和1.4倍, DNA结合活性则从2.8和3.7倍分别降为1.1和1.5倍),而蛋白酪氨酸磷酸酶抑制剂矾酸钠则能明显地促进他们的增高(磷酸化水平从2.0倍增到3.4倍, DNA结合活性从3.1倍增为5.1倍)。

Proteomic comparison of glucose- and lactose-grown cells revealed that lactose and glucose were catabolized via the same degradation pathway, and the rate of glucose assimilation was higher than that of lactose.

长双歧杆菌NCC2705在乳糖中生长快于葡萄糖,它们的降解途径是相同的;转醛缩酶和丙酮酸激酶发生了翻译后修饰作用,推测转醛缩酶在43T和47S发生了磷酸化,而丙酮酸激酶在65S发生了磷酸化。

Analysis of the digestion of lysyl endopeptidase and N-terminal amino-acid sequence showed that Thr204 was the phosphorylated site which was consistent with the phosphorylation of Thr199 in DnaK.

赖氨酰肽链内切酶酶切、反相分离、氨基酸测序确定磷酸化位点为204位苏氨酸,与大肠杆菌Hsp70---DnaK的199位苏氨酸磷酸化一致。

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