脫酰酶 的英文怎麼說
中文拼音 [tuō]
脫酰酶
英文
coa-
We present a preliminary study on the zymograms of esterase ( est ), lactate dehydrogenase ( ldh ), malate dehydrogenase ( mdh ) from four groups of microtus fortis by vertical discontinous polyacrylamide gel electrophoresis method. the number, mobility and dye intensity of the enzyme band were analyzed
採用垂直板不連續聚丙烯酰胺凝膠電泳法對四類東方田鼠的酯酶( est ) 、蘋果酸脫氫酶( mdh )和乳酸脫氫酶( ldh )進行了初步研究。The common biosynthesis pathway of aromatic amino acids includes seven steps from dahp to chorismate acid. for the common pathway, 3 - dehydroquinate ( dhq ) synthase ( encoded by arob ), 5 - enolpyruv - oylshikimate s - phosphate ( epsp ) synthase ( encoded by aroa ), and chorisma - te synthase ( encoded by aroc ] are rate - limiting enzymes
芳香族氨基酸的合成步驟有七步是共同的,亦即從dahp到分支酸的合成步驟,其中脫氫奎寧酸合成酶( arob ) 、 5 -烯醇式丙酮酰莽草酸合成酶( aroa )和分支酸合成酶( aroc )是此代謝途徑的關鍵酶。The association of gene polymorphisms of mgp and alad with lead blood level in children
羧基谷氨酸蛋白和氨基乙酰丙酸脫水酶基因多態性與兒童血鉛的關系High - property chitosan can be produced by chitin deacetylase
而採用甲殼素脫乙酰酶能制備出性能獨特的殼聚糖。In this paper, advances in the application and research of chitin deacetylase in preparation of chitosan are summarized
本文就甲殼素脫乙酰酶在殼聚糖制備中的應用及研究進展作一綜述。Nitrate is converted to ammonium by nitrate reductase and ammonium is then incorporated into glutamine and gluamate, either by the glutamine synthase - glutamate synthase ( gs - gogat ) pathway or by glutamate dehydrogenase ( gdh )
硝酸鹽在硝酸還原酶作用下被轉化為銨,接著所產生的銨在谷氨酰胺合成酶-谷氨酸合酶( gs - gogat )或谷氨酸脫氫酶( gdh )的作用下與谷氨酰胺和谷氨酸結合。- acetolactate decarboxylase is purifed from cell extract by 50 % - 80 % ammonium sulfate - fractionation, 50, 2min heat treatment and deae - sepharose fast flow column chromatography, which we study the different ph and different buffer of deae - sepharose fast flow column chromatography and conclude ph 6
對其酶學性質進行了研究。 -乙酰乳酸脫羧酶經50 80硫酸銨分級沉澱、 50 , 2min熱處理、 deae - sepharosefastflow離子交換柱層析方法分離純化。- acetolactate decarboxylase are widely found among bacterial strains but not in other groups of organisms. the enzyme has been demonstrated to be effective for removal of acetolactate and widely used in beer product. in this paper, - acetolactate decarboxylase from bacillus subtilis was purifed to homogeneity from cell extract by ammonium sulfate - fractionation, heat treatment, deae - sepharose fast flow column chromatography
本文對來源於枯草芽孢桿菌( bacillussubtilis ) 3226 - 5的-乙酰乳酸脫羧酶經硫酸銨分級沉澱、熱處理、 deae - sepharosefastflow離子交換柱層析等分離純化步驟,得到sds - paeg電泳純,通過n末端氨基酸序列分析驗證酶蛋白的純度。Changes of enzyme and biology in the fermented grains for hengshui laobaigan - flavor liquor
乙酰乳酸脫羧酶的儲存初探By using the polyacrylamide gel electrophoresis, thirteen isozymes ( est, sod, gd, gpi, mdh, me, cat et al., ) from five population of r. philippinarum in the north of china were analised and compared
通過聚丙烯酰胺凝膠電泳對中國北方五個群體的菲律賓蛤仔的酯酶、超氧化物歧化酶、葡萄糖六磷酸脫氫酶、蘋果酸脫氫酶、磷酸葡萄糖異構酶、蘋果酸酶和過氧化氫酶等同工酶進行了分析比較。Acetylornithine deacetylase is the key enzyme of producting l - methionine. we mainly do research work on the construction of acetylornithine deacetylase gene - engineering strain and characteristic of proteinase. in order to get high expression deacetylase strain, we obtain the gene by pcr arge gene. the product ( 2800bp ) was cloned into puc19 plasmid and confirmed with blue / white dot screening > restriction enzyme analysis and pcr. then taking the nucleotide sequencing compared with the sequence at blast of u. s. a. we constructed a high expression of gene - engineering strain - pxj 128 which containing the arge gene on the high expressing system of pxji18 with activity of acetylornithine deacetylase above 20000u / g
為了獲得高效表達的脫乙酰鳥氨酸酶工程菌株,在工程菌技術改造及其固定化研究做了進一步的研究和探討。我們採用基因工程技術,通過pcr技術擴增出了酰化酶關鍵酶基因?脫乙酰鳥氨酸酶基因arge ,將其克隆到puc19載體中,經酶切鑒定、 pcr鑒定篩選出重組陽性質粒,並測序鑒定,通過美國blast程序進行了基因數據庫相似性比較分析。Methods : in cultured lung explants without serum, the lipid component synthesis of pulmonary surfactant was evaluated in [ 3h ] - choline incorporation ; mrna content of phosphocholine cytidylyltransferase ( cct ) in lung explants was investigated in rt - pcr ; the changes of the ultrastructure of the at ii cells were observed with electron microscope ; the expression of nmdar1 subtype was observed in immunohistochemistry staining ; nitric oxide synthase ( nos ) activity, nitric oxide ( no ) content, superoxide dismutase ( sod ) level, malondialdehyde ( mda ) content and lactae dehydroase ( ldh ) level were determined by biochemistry methods. results : 1. influence of glutamate on synthesis of the lipid component of pulmonary surfactant ? with l - arginine, glu inhibited [ 3h ] - choline incorporation with good dose - dependence and time - dependence ; ( 2 ) mrna content of cct of the glu treatment groups was decreased ; ( 3 ) glu increases the release of ldh in cultured lung explants ; ( dwith electron microscope histochemistry, glu induced the changes of the ultrastruture of at ii iv cells
方法:採用成年大鼠肺組織無血清培養,運用[ ~ 3h ] -膽堿摻入法測定ps主要脂質磷脂酰膽堿( pc )合成量; rt - pcr擴增檢測肺組織中pc合成限速酶磷酸膽堿二胞苷酰基轉移酶( cct ) mrna含量;透射電子顯微鏡法觀察肺泡型上皮細胞和ps系統超微結構的變化;免疫組織化學染色檢測glu的受體nmdar1亞單位的表達;生化測定肺組織乳酸脫氫酶( ldh )釋放量和肺組織勻漿中一氧化氮合酶( nos )活性、一氧化氮( no )生成量、超氧化物歧化酶( sod )水平以及丙二醛( mda )含量。Platelet - activating factor acetylhydrolase and cardiovascular disease
血漿血小板激活因子酰基脫水酶與心血管疾病分享友人