酶抑制測定 的英文怎麼說

中文拼音 [yìzhìcèdìng]
酶抑制測定 英文
enzyme-inhibition assay
  • 酶 : 名詞[生物化學] （生物體的細胞產生的有機膠狀物質） enzyme; ferment
  • 抑 : Ⅰ動詞（向下按; 壓制） restrain; repress; curb Ⅱ連詞[書面語]1 （表示抉擇） or 2 （表示轉折） but3 ...
  • 制 : Ⅰ動詞1 （製造） make; manufacture 2 （擬訂; 規定） draw up; establish 3 （用強力約束; 限定; 管束...
  • 測 : 動詞1. （測量） survey; fathom; measure 2. （測度; 推測） conjecture; infer
  • 定 : Ⅰ形容詞1 （平靜; 穩定） calm; stable 2 （已經確定的; 不改變的） fixed; settled; established Ⅱ動詞...
  • 抑制 : 1 （控制） restrain; control; check; hold up; curb; stop; repress; bridle; choke; prehension; sup...
  • 測定 : determine; determination; setting-out; admeasurement; assignment; assay; finding
  1. Based on the extensive studies of subtilisin - like protease ( prl ) of metarhizium anisopliae, extracellullar serine protease is suggested to be a key enzyme involved in the fimgal penetration to invertebrates. the investigation of serine protease in the nematode infected by owvtl may help to understand the mechanism of nematophagous fimgi as biological control agents. a 3l kda serine protease was isolated and purified from the liquid culture of h rhossiliensis owvtl challenged with nematode panagrellus redivivus

    本研究利用線蟲誘導下owvt - 1菌株液體發酵，通過粗分級分離、離子交換層析和凝膠過濾層析分離提純了一個分子量為31kda的絲氨酸蛋白酶，生物學測定表明其對大豆胞囊線蟲二齡幼蟲具有致死作用，同時測定了該酶理化特性，酶活力在75附近酶活力最高，隨著ph的增加酶的穩定性升高，與膽堿酯酶具有相似的ph曲線，對特異性底物aape （ suc - ala - ala - pro - glu - pna ）具有作用， ssi和ci - 2抑制該酶的活性。
  2. Measurement of trypsin inhibitor activity of soya - bean products

    大豆製品中胰蛋白酶抑制劑的抑制活性測定
  3. Animal feeding stuffs - determination of trypsin inhibitor activity of soya products

    動物飼料.大豆製品胰蛋白酶抑制劑活性的測定
  4. The a - transglucosidase was selectively modified by pcmb, me, edc, clac, acetyl acetone and nbs, and changes in the activities of the enzyme have been detected. the reaction of a - transglucosidase with pcmb, me, edc and clac resulted in a strong inhibition of the enzyme activities which decreased with the increase of modifier concentration. the acetyl acetone and nbs were found without inhibition effect

    酚丙酮、小涅代唬拍酷亞胺剛b引等化學修飾劑對a葡萄糖轉苦酶的幾種氨基酸殘基進行選擇修飾，並測定其酶活力變化，結果表明： pcmb 、 me 、 edc 、 ciac能顯著抑制酶的活性，活力的下降與修飾劑的濃度有關，乙酚丙酮、 nbs白巾飾對酶的奪製作用不明顯。
  5. In escherichia coli, arog gene encodes phenylalanine - sensitive 3 - deoxy - d - arabino - heptulosonate - 7 - phosphate synthase isoenzyme arog that catalyzes the first committed step of shikimate pathway. here we study the essential amino acid residues involved in the formation of feedback inhibition site of arog, and the effects of n - terminus on feedback inhibition and its quaternary structure, and the importance of the structural " d2 " symmetry to allosteric inhibition

    本博士論文工作以大腸桿菌k - 12來源的arog為研究對象，通過定點突變、反饋抑制實驗和酶學動力學參數的測定，深入地研究了arog的反饋抑制位點的特性，並對arog的n -末端在反饋抑制機理和維持穩定四級結構中的作用，以及蛋白質結構的「 d2 」對稱性對酶功能的重要性等進行了具體的研究。
  6. At the cadmium concentration of 2. 19mg / l and 4. 37mg / l, for 72h, the na + - k + - atpase activity of kidney tissues were decreased very significantly. the higher of the concentration of cadmium or the longer of the exposure the more the enzymic activity was decreased. the na + - k + - atpase activity of gill tissues were decreased but not significantly at the low concentratioin of cadmium

    對na ~ + - k鍋離子對草魚魚種組織sod和atpase的影響及毒性研究atp酶的活性測定表明，與對照組相比， cd 》對草魚魚種鰓和腎的na k atp酶活性均有抑制作用，這種抑制作用隨著暴露時間的延長而加強。
  7. Levels of fasting blood glucose and 24h urinary microcontent of albumin 24 h malb were determined dynamically ; the serum glycosyl hemoglobin hba1c was determined after the last medication ; the ultrastructural changes of kidney were observed by transmission electron microscope ; the expressions of collagen, fibronctin, laminin ln, and the ecm metabolism influencing factors, including mmp2, tissue inhibitor of metalloproteinase timp2, transfer growth factor 1 tgf 1 in renal tissue were detected by immunohistological chemistry and image collecting analytical system

    動態檢測各組大鼠空腹血糖fbg 24h尿微量白蛋白24h malb ，末次給藥后測定大鼠血漿糖化血紅蛋白hba1c透射電鏡觀察各組大鼠腎臟超微結構改變，應用免疫組化技術及圖像採集分析系統測定各組大鼠腎臟組織中型膠原c纖維連接蛋白fn層粘連蛋白ln的表達，測定影響ecm代謝的基質金屬蛋白酶2 mmp2基質金屬蛋白酶抑制劑2 timp2及轉化生長因子1 tgf 1的表達。
  8. Based on the principle of enzyme inhibition, using the immobilized chicken liver esterase and a flow injection analysis ( fia ) enzyme biosensor ( developed by ourselves ), this paper investigated the inhibiting power of several insecticides to the enzyme, and selected methamidophos as the standard pesticide for the quantitive determination

    摘要本文基於酶抑制原理，採用固定化雞肝酯酶和自行研製的流動注射式酶生物傳感器，研究了不同農藥對酶的抑製程度，確定了甲胺磷作為農藥檢測的定量標準。
  9. With the results of analysis of cells morphology and cell cycle determination, c. chinensis extract, inhibiting pc 12 cells proliferation, inducing neurite outgrowth, was testified. at the same time, c. chinensis extract can also amplify expression of neuroregenerating maker molecule, growth associated protein - 43, increase the activity of acetylcholinesterase in rat pheochromocytoma pc 12 cells

    菟絲子提取物處理后的pc12細胞形態分析、免疫組化和細胞周期測定結果表明，菟絲子提取物不僅能抑制細胞分裂，誘導細胞分化、延伸大量突起，而且能促進神經元再生信號蛋白gap - 43的大量表達，提高乙酰膽堿脂酶（ acetylcholinesterase ， ache ）的活性。
  10. It was observed that the treatment of seedlings with 50 mol / l al for 12h led to a remarkable inhibition of root growth, which was accompanied by sufficient efflux of citrate out of roots and increase in the citrate content in the root tips

    結果表明： al處理明顯抑制根的生長， 20 mol lal處理12h對c . tora根生長的抑制達52 . 4 。為了搞清al誘導c . tora根系檸檬酸分泌的生化與生理基礎，我們測定了與檸檬酸代謝直接有關的幾個酶的活性。
  11. The positive transformants with the integrates mn - sod gene was identified by zeocin - resistance, pcr screening and expression in p. pastoris. the recombinant mn - sod protein was successfully expressed in pichia pastoris based on the evidences that a relative molecular weight about 23kd appeard in sds - page, the obvious activity of sod existed in native - page and enzymatic activity test, and mn - sod activity was specific base on the inhibition with the mixture of chloroform - enthanol ( 3 : 5 / v : v ) and potassium cyanide. two secreted plasmids ppiczaa - sodm18 and ppiczaa - sodc were constructed and after there linearization were transferred into chromosome of pichia pastoris gs115 by electroporation

    Pcr鑒定及mut表型分析進一步說明，目標基因已經重組到宿主菌基因組染色體上； 0 . 5甲醇誘導表達后， sds - page結果顯示，表達的蛋白相對分子量約為23kd ，活性電泳出現明顯活性條帶；酶活性測定顯示，重組菌株sod活性比對照提高5倍左右；氯仿-乙醇（ 3 : 5 v : v ）和kcn （ 5mmol l ）抑制反應進一步證明，所表達的sod為錳超氧化物歧化酶。
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