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carboxylase相关的网络例句

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与 carboxylase 相关的网络例句 [注:此内容来源于网络,仅供参考]

The activity of pyruvate carboxylase depends on the presence of acetyl CoA so that more oxaloacetate os made when acetyl CoA levels rise.

丙酮酸羧化酶的活性依赖于乙酰-CoA 的存在。因此,当乙酰-CoA,水平上升时,会产生更多的草酰乙酸。

Different position's leaves had different light compensate point and light saturate point and apparent quantum efficiency and CO〓 compensate concentration and CO〓 saturate concentration and carboxylase efficiency in the different season.

不同生长季节不同部位叶片的LCP、LSP、α和CO〓补偿点、CO〓饱和点、羧化效率上存在较大的差异。

Sequencing revealed that the most common genes appearedin the library is photorespiratory-related genes, such as ribulose bisphosphate carboxylase, Rubisco activase, glyoxylate aminotransferase, glutamine synthetase,glyceraldehyde dehydrogenase, ferredoxin, transport protein, etc.

测序之后发现最为显著的是一些光呼吸相关的基因如核酮糖-1,5-二磷酸羧化/加氧酶、Rubisco激活酶、乙醛酸转氨酶、谷氨酸转氨酶、甘油醛脱氢酶、铁氧还原蛋白和转运蛋白等。

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。

Purified protein samples were separated by 2-DE with 17 cm IPG strips, and the protein spots were detected by fast silver staining. Six protein spots were randomly excised from the silver stained gel for primary analysis by MALDI-TOF MS. Four proteins were identified, and they were 1-aminocyclopropane-1-carboxylate synthase 2, ribulose-1, 5-bisphosphate carboxylase/oxygenase large subunit, F11O4.2 and Rubisco small subunit.

根据预实验结果,选用17 cm IPG预制干胶条对纯化的蛋白样品进行2-DE实验,采用快速银染法进行染色,随机挖取银染胶上6个蛋白点进行MALDI-TOF MS分析和数据库检索,鉴定了3个蛋白,它们是:1-氨基环丙烷-1羧酸合酶2,核酮糖-1,5-二磷酸羧化酶/加氧酶大亚基和F11O4.2。

With the aid of PDQuest 2-DE software, 11 significant protein dots were found out and then 9 of them are pick out to go through peptide mass fingerprinting based on MALDI TOF MS and NCBI database searching . In all, 5 proteins were identified: Ribulose bisphosphate carboxylase , Nucleic acid-binding protein , Ribosomal protection tetracycline resistance protein , hypothetical protein FG04726.1 [Gibberella zeae PH-1], nitric oxide synthase .

应用PMF技术对这11个具有显著表达差异蛋白点中的9个进行鉴定,得到了5个质谱阳性鉴定结果,其中2个蛋白分别为玉米种属的1,5-二磷酸核酮糖羧化酶/加氧酶和叶绿体的核酸结合蛋白;其它的3个蛋白在玉米蛋白质数据库中未见报道,但与其它物种基因编码的蛋白质具有高度的序列同源性。

In these chloroplasts carbon dioxide combines with phosphoenolpyruvate to form oxaloacetic acid, which is transported to the bundle sheath cells, where the carbon dioxide is released, then fixed by the enzyme ribulose bisphosphate carboxylase to form glycerate 3-phosphate, the first step in the Calvin cycle.

在叶肉细胞的叶绿体中二氧化碳与磷酸烯醇丙酮酸结合形成草酰乙酸,后被运到邻近的维管束鞘细胞,在那里二氧化碳被释放,后被核酮糖二磷酸羧化酶固定形成3-磷酸甘油酸,这是卡尔文的循环第一步。

The results showed that TNF-α effectively inhibited preadipocyte proliferation stimulated by insulin and decreased lipogenesis through inhibiting stimulation of insulin on transcriptional expressions of lipogenic genes such as acetyl-CoA carboxylase α(ACC1), fatty acid synthase, sterol regulatory element binding protein-1c in adipocytes, suggesting that TNF-α is a effective inhibitor of adipogenesis in adipose tissue.

结果表明,TNF-α可有效抑制胰岛素对原代培养大鼠前体脂肪细胞增殖的促进作用,并通过抑制胰岛素对转录因子SREBP-1c和脂肪酸合酶FAS及ACC1基因转录表达的促进作用,减少脂肪酸的生物合成,抑制成熟脂肪细胞的脂肪生成,证明TNF-α是动物脂肪形成的有效抑制因子。

The pathway The first committed step in Fatty acid biosynthesis is the carboxylation of acetyl CoA to form malonyl CoA which is catalyzed by the biotin-containing enzyme acetyl CoA carboxylase.

途 径 脂肪酸合成的第一个关键步骤是乙酰-COA 羧基化形成丙二酰单酰 COA ,这一步是在含生物素的酶乙酰-COA 羧化酶的催化下进行的。

On the successful basis of bovine hepatic cell culture and competitive DNA template of pyruvate carboxylase gene,effects of propionate sodium and pyruvate sodium on mRNA of PC gene in cultured bovine hepatocyte in vitro was determinated quantitively by competitive RT-PCR.

在成功构建牛肝细胞培养模型和PC基因DNA竞争模板的基础上,采用竞争RT-PCR方法检测了丙酸钠和丙酮酸钠对体外培养新生牛单层肝细胞PC基因mRNA丰度的影响。

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