脫酰氨基酶 的英文怎麼說

中文拼音 [tuōān]
脫酰氨基酶 英文
deamidase
  • : Ⅰ動詞1 (脫落) cast; shed; drop; fall off 2 (取下; 除去) take off; strip; cast off 3 (脫離) ...
  • : 名詞[化學] (酰基) acyl
  • : 名詞[化學] (氮和氫的化合物) ammonia; hydrogen nitride
  • : 名詞[生物化學] (生物體的細胞產生的有機膠狀物質) enzyme; ferment
  • 氨基 : amido group
  1. 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,其中氫奎寧酸合成( arob ) 、 5 -烯醇式丙酮莽草酸合成( aroa )和分支酸合成( aroc )是此代謝途徑的關鍵
  2. The association of gene polymorphisms of mgp and alad with lead blood level in children

    酸蛋白和丙酸因多態性與兒童血鉛的關系
  3. - 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-乙乳酸經硫酸銨分級沉澱、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末端酸序列分析驗證蛋白的純度。
  4. 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。我們採用因工程技術,通過pcr技術擴增出了關鍵因?因arge ,將其克隆到puc19載體中,經切鑒定、 pcr鑒定篩選出重組陽性質粒,並測序鑒定,通過美國blast程序進行了因數據庫相似性比較分析。
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