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The results showed that:(1) 5'-nucleotide contents in yeast autolysate was slightly increased by adding RNase frommalted barley roots;(2) higher pH did not improve the 5'-nucleotide contents even in the presence of RNase from malted barleyroots, but at the pH 8.0, the addition of Acalase could increase the final yield, soluble protein contents and 5'-nucleotide inthe presence of RNase from malted barley roots.

酵母核酸酶的pH稳定性和温度稳定性均比麦芽根核酸酶的要差。这说明自溶法生产酵母提取物时,即使外加5'-磷酸二酯酶不能有效提高呈味核苷酸的原因并非由于外加的5'-磷酸二酯酶性质不稳定,而是另有其它原因。

They were named respectively as muramidase-released protein; succinate dehydrogenase/fumarate reductase flavoprotein subunit (SDHFp/FRDFP, extracellular); bacterial trigger factor; elongation factor G (EF-G, extracellular); PTS system sorbose subfamily I (PTS/MAN-ⅡAB, cytoplasmic); pyruvate kinase; phosphofructokinase, PK.

经MALDI-TOF-MS鉴定,这8个蛋白分别为溶菌酶释放蛋白、琥珀脱氢酶/延胡索酸还原酶黄素蛋白亚单位(SDHFp/FRDFp)、触发因子、延长因子G、细菌糖磷酸转移酶系统甘露糖特异ⅡAB亚单位、丙酮酸激酶、6-磷酸果糖激酶(6-PFK)、色氨酸-tRNA合成酶。

Phosphoglycerate mutase is a key enzyme in glycolytic pathways. With PCR technique based on an EST identified in our lab, a novel gene named SjPGAM GenBank Accession No.

磷酸甘油酸变位酶是糖酵解过程中的一种重要酶,主要催化3-磷酸甘油酸转化为2-磷酸甘油酸。

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。

The result makes clear, ADPG anxious phosphation is enzymatic with amylaceous branch enzymatic be spring processing of 200 Kg/hm2 of nitrogen of Shi Chun of enzymatic; of key of complex of jade rice starch is to rise spring enzymatic active of corn ADPG anxious phosphation and raise this Yo 9, in safety 18, 4 odd 19 Q.

结果表明,ADPG焦磷酸化酶和淀粉分支酶是春玉米淀粉合成的关键酶;施纯氮200 kg/hm2处理是提高春玉米ADPG焦磷酸化酶活性和提高本育9、平安18、四单19 Q酶活性的最佳处理;施纯氮100 kg/hm2处理是提高丰禾10Q酶活性的最佳处理。

In this review, the biosynthetic pathway of ginsenosides was introduced and the research progress on enzymes related to ginsenoside biosynthesis , such as 3-hydroxy-3-methyl-glutaryl-CoA reductase, geranyl pyrophosphate synthase, farnesyl pyrophosphate synthase, was summarized in detail.

本文综述了人参皂苷的生物合成途径,并介绍了3-羟基-3-甲基戊二酸CoA还原酶、牻牛儿基二磷酸合成酶、法尼基二磷酸合成酶等人参皂苷合成途径相关酶的研究进展。

PartⅡThe mechanism elucidation about effects ofα-(2,3)/(2,6)sialic acid on the Cx43gap-junction functions.(1) Westernblotting experiment showed that the decrease of sialic acid didn\'t changethe Cx43 expression and its phospholation level.(2) Westernblotting experiment showed sialidase didn,t change the ZO-1 expression,IP and confocal experiment showed sialidase improved the interaction of Cx43 andZO-1.(3) Westernblotting experiment showed sialidase didn\'t change N-cadherin expression,IP and confocal experiment showed sialidase promoted the complex formation ofCx43 and N-Cadherin.(4)Sialidase could increase the ERK1/2 phospholation level,and enchanedintercellular homotypic adhesion,Immunofluorometric assay showed sialidase couldpromote the N-cadherin cluster on the membrance.

第二部分:α—(2,3)/(2,6)唾液酸对肿瘤细胞CX43间隙连接功能影响的机制研究1、Westernblotting结果表明降低细胞膜表面唾液酸并不改变Cx43的表达及其磷酸化水平:但Cx43连接斑形成增多;2、Westernblotting结果表明唾液酸酶作用后细胞ZO—1表达没有改变,IP及免疫荧光共定位结果表明唾液酸酶作用后促进了Cx43与ZO-1的结合;3、Westernblotting结果表明唾液酸酶作用后细胞N-cadherin表达没有改变,IP及免疫荧光共定位结果表明唾液酸酶作用后促进了Cx43与N-Cadherin复合物的形成;4、唾液酸酶作用后细胞内ERK1/2磷酸化水平明显增加,细胞间同质粘附增加,以及免疫荧光表明唾液酸降低后可促进N-cadherin的膜成簇。

Beside the catalysis in transferring the high energy phosphate bond from ATP to NDP, NDPKs also show the activities of NDP kinase and proteinic phosphotransferase.

该酶除了催化腺苷三磷酸和核苷二磷酸之间高能磷酸基团的转移外,还具有NDP激酶活性和蛋白磷酸转移酶活性,并参与转录调控和信号转导。

Glycogen degradation and glycogen synthesis are controlled both by allosteric regulation and by hormonal control.

糖原分解及合成的主要酶是磷酸化酶及糖原合成酶,它们的活性是受磷酸化和去磷酸化的共价修饰调节及变构效应的调节。

Simultaneously, the activity and coding gene expression of ribulose 1, 5-bisphosphate carboxylase, phosphoenolpyruvate carboxylase, and glycollic oxidase all decrease in two rice accessions under low potassium supply while significant decrease in non-allelopathic rice "Lemont".

水稻光合作用相关酶的分析结果表明,低钾条件下核酮糖-1,5-二磷酸羧化酶、磷酸烯醇式丙酮酸羧化酶和乙醇酸氧化酶的活性及其基因表达强度均降低,但化感水稻&PI312777&的下降幅度显著小于非化感水稻&Lemont&。

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