氧還酶 的英文怎麼說
中文拼音 [yǎnghái]
氧還酶
英文
oxido-reductase-
Synthesis and aldose reductase inhibitory activity of - phenylmethylene - - oxo - benzenepropanoic acid derivatives
氧代苯丙酸衍生物的合成及其醛糖還原酶抑制活性Ppo ? a mixture of monophenol oxidase and catechol oxidase enzymes ? is present in nearly all plant tissues and can also be found in bacteria, animals and fungi
幾乎所有的植物組織都含有多酚氧化酶,多酚氧化酶還存在於細菌、動物和真菌類植物身上。The results showed that the cucumber seeds soaked with extracts of total alkaloid, dissoluble alkaloid and fat - soluble alkaloid from p. multisectum ( maxim. ) bobr., the activities of amylase, protease and lipase during seed germination were inhibited, the seed vigor and germination rate were suppressed, and respiration rate of seedling was slackened ; root activity, chlorophyll content and activities of nitrate reductase, superoxide dismutase sod ) and peroxidase ( pod ) of cucumber seedlings during seedlings growth were increased
結果表明,多裂駱駝蓬總生物堿提取液、水溶性生物堿提取液和脂溶性生物堿提取液浸種均抑制黃瓜種子萌發過程中澱粉酶、蛋白酶和脂肪酶活性,種子活力和萌發速率降低,呼吸速率減慢;幼苗生長過程中根系活力、硝酸還原酶活性升高,葉綠素含量增加,超氧化物歧化酶( sod )和過氧化物酶( pod )活性提高。Because of the cleavage site of enterokinase and cnbr was designed in the middle of thioredoxin and cmiv, the expressed peptides of the mutation of cmiv could be cuted down from the fusion protein by enterokinase or cnbr
由於硫氧還蛋白和抗菌肽之間設計了腸激酶( enterokinase )切割位點和cnbr切割位點,通過對該表達的融合蛋白的切割,可得到目標抗菌肽cmiv突變體多肽分子。Many enzymes require metal cofactors, e. g. ferredoxin requires ferrous and ferric ions
許多酶都需要金屬的輔助因子,例如鐵氧還蛋白就需要鐵離子。The other is ferredoxin / thioredoxin system located in nonphotosynthetic tissue and cytosol of photosynthetic cell, which includes ferredoxin, ferredoxin dependent thioredoxin reductase, thioredoxin h. this two system constitutes important cellular redox regulatory system and can regulate the redox intercellular environment, metablism and signaling transduction
另一個是nadp ( h ) -硫氧還蛋白系統,該系統是由h -型的硫氧還蛋白、 nadp ( h ) 、和依賴于nadp ( h )的硫氧還蛋白還原酶(一種黃素蛋白)組成。In the present dissertation, summarized and reviewed senior ' s study of lespedeza michx., on the basis of this, studied plants of lespedeza michx. in inner mongolia by means of polynology and cladistics taxology, discussed part of controversial species with menthod of and peroxidase isoenzyme pattern analysis
本文在回顧和總結前人對胡枝子屬lespedezamichx .植物研究的基礎上,對在內蒙古分佈的胡枝子屬植物進行了支序分類學和孢粉學研究;還對部分有爭議的種類做了過氧化物酶同工酶酶譜分析。Expression of human nad h : quinone oxidoreductase 1 gene induced by antioxidants and hypoxia and the mechanism
抗氧化劑和低氧誘導醌氧化還原酶1基因的表達及其機制The effort of manganese removal was studied and the kinetics of manganese removal was tried to establish. the factors of dissolved oxygen concentration, fe2 + concentration, ph, p concentration and closing of the filter were studied to evaluate their effort for biological manganese removal, and the correlation of residual manganese and oxidation - reduction potential was also discussed. as the iron content of water was high, experiment results showed that the reaction was zero order, as the iron content of water was low, the reaction was first order. the time needed for the cultivation of biological manganese removal was 60 70 days. the filter operated at the filtration rate of 8 10m / h, silica sand of effective size 0. 95 1. 25mm filled the filter to a depth of 1200mm
試驗結果表明,成熟后濾砂表面濾膜的x射線衍射圖譜與mno _ x ? 5h _ 2o ( x = 1 . 86 )的x射線衍射圖譜一樣,濾膜成熟后的結構在進水物質不發生變化的情況下不發生變化;合適的碳磷比對生物除錳有明顯的促進作用,試驗條件下的投磷量不會對出水造成二次污染;生物除錳需要亞鐵的參與,亞鐵的存在除了能夠促進微生物分泌胞外酶並刺激其活性外,還通過鐵離子的變價傳遞電子,催化錳離子的氧化反應,從而促進對二價錳的降解。The metabolism of these extreme microbes during the production of maotai liquor would further produce multiple enzymes of thermal stability such as amylase, protease, saccharifying enzyme, cellulose, glucase, xylanase, and each kind of dehydrase involved in redox reaction, and dna polyase etc
茅臺酒釀造過程中極端釀酒微生物代謝產生多種熱穩定性的酶,如澱粉酶、蛋白酶、糖化酶、纖維素酶、葡萄糖甘酶、木聚糖酶、參與氧化還原反應的各種脫氮酶、磷酸烯醇丙酮酸激酶及dna聚合酶等。Now, new findings suggest that the drug achieves this by cutting off the tumor ' s blood supply, not just by blocking an enzyme called cyclooxygenase
現在,新發現表明阿司匹林的這種作用不僅僅是通過阻斷環氧合酶,而且還能切斷腫瘤血液供應來實現的。The nucleotide ( nt ) sequence of the insert in phz1754 is 2299bps in size. computer assisted analysis of the sequence revealed an open reading frame ( orf ) with a g + c content of 70. 3 % that would encode a protein of 552 amino acids ( aa ). the nt seque nce comparision revealed that the orf in the sequenced region exhibits 85 % dna sequence homology with the cholesterol oxidase gene choa of streptomyces sp
對phz1754進行外切核酸酶( exonuclease , exo )順序缺失,獲得單向長度漸減重疊的系列突變體,核苷酸序列測定顯示出該ecor - sal片段的精確大小為2299bps , frameplot程序分析揭示出該區域一個完整的開放閱讀框( orf )的存在,其大小為1656bps , g + c含量為70 . 3 ,編碼552個氨基酸,利用blastsearch程序將orf的核苷酸序列及推導的氨基酸序列與因特網上基因及蛋白質數據庫進行綜合比較,發現無論在核苷酸水平還是在蛋白水平上,該orf均與膽固醇氧化酶表現出同源性,而且與鏈黴菌膽固醇氧化酶同源性最高,說明該orf編碼膽固醇氧化酶基因。Both the mature genes of gloshedobin and gussurobin were cloned into the vector pet - 32a ( + ), strain bl21 ( de3 ), to study their expression in prokaryotic cell. the gene was expressed under t7 promoter with a fusion protein partner of thx. tag and a 6x his. tag at its n - terminal. having been induced by iptg for 4 hours, the recombinant enzyme was examined in the cytoplasm by sds - page analysis
將大連蛇島蝮蛇和長白山白眉蝮蛇毒類凝血酶基因分別克隆到大腸桿菌表達載體pet - 32 ( a ) +中,在t7啟動子下表達出融合蛋白,融合部分為硫氧還蛋白,位於類凝血酶基因上游,並在其n端帶6xhistag標簽以利於表達產物的分離純化,經熱激轉化至宿主菌bl21 ( de3 )中, iptg誘導斗小時后收獲菌體。The electrons are transferred along the chain to a carrier molecule ( coenzyme q ), and then in sequence to a series of cytochromes, finally acting with the enzyme cytochrome oxidase to reduce an oxygen atom, which combines with two h + ions to form water
電子沿呼吸鏈傳遞到載體分子? ?輔酶q上,然後依次經過一系列細胞色素分子的傳遞,最後與細胞色素氧化酶反應,氧原子結合兩個氫形成水從而被還原。Its catalytic current was linear with the concentration of h2o2. most of interference was effectively eliminated and the inactivity of hrp under the too low potential to catalytize the reduction of h2o2 was avoided due to the enhanced potential of nr by zp in the composite film. while the silver colloid in the composite film enhanced the capability of zp to adsorb nr and prevented effectively nr from leaching off
4 、上修飾電極與辣根過氧化酶相耦合製成酶電極,顯著的催化了過氧化氫的還原,磷酸鋯提高了中性紅的氧化還原電位,大大的降低了測定的干擾,並有效的避免了辣根過氧化酶在過低的還原電位下失效,納米銀增強了膜對中性紅的吸附,有效的防止了其流失。L l6 - hsd2 is localized to the sppytiotrophoblast of the placenty providing a fimctional barrier protecting the fetus from matemal glucocorticoids. a sequence resembling glucocorticoid response element ( gre ) has been identified in the promoter region of the human l l0 - hsdl gene. glucocorticoids have been shown to induce the expression of 11p - hsdl in the hippomus in vitro " whereas controversial results were obtained in the hepatocyte
體內至少存在兩型11 - hsd ,在細胞完整的狀態下, 11 - hsd1主要為還原酶,它活化gc的代謝產物17 -羥- 11 -脫氫皮質酮(嚙齒類為脫氫皮質酮)為有活性的皮質醇(嚙齒類為皮質酮) ,而11 - hsd2為氧化酶,它催化皮質醇為無活性的17 -羥- 11 -脫氫皮質酮,因此11 - hsd1加強gc的作用,而11 - hsd2減弱gc的作用。The paper summarize some relevant data and introduces the current research situation about the offects of intragen on photosynthesis, chlorophyll, photosynthetic rate, effeciency of solar energy utilization, dark reaction and photorespiration etc., on respiration and on some metabolic enzymes, including nitrate reductase, enzyme protective system of membrane - lipid peroxidation
綜合國內外有關文獻,介紹了氮素對植物光合作用(包括光合色素、光合速率、光能利用率、光合暗反應、光呼吸等) 、呼吸作用和一些代謝酶(包括硝酸還原酶、膜脂過氧化酶促防禦系統)的影響。This study was to investigate the effects of sulfur dioxide inhalation at different concentrations on some glutathione - related enzymes such as glutathione s - transferase ( gst ), glucose 6 - phosphate dehydrogenase ( g6pd ) and glutathione reductase ( gred ) in brain, lung, heart, liver, kidney and spleen of mice by the technology of biochemical toxicology. the results were showed as follows, so2 exposure at different concentrations caused the changes of glutathione redox system. moreover, the activities of antioxidative enzymes and the contents of reduced glutathione ( gsh ) were decreased significantly in different tissues at higher concentrations of soa
本研究利用生化毒理學技術研究了不同濃度二氧化硫吸入( 22 2mg m ~ 3 , 64 3mg m ~ 3 , 148 23mg m ~ 3 )對純系昆明小鼠腦、肺、心、肝、腎、脾六種組織的谷胱甘肽還原酶( glutathionereductase , gred ) 、谷胱甘肽硫轉移酶( glutathiones - transferase , gst )和葡萄糖- 6 -磷酸脫氫酶( glucose6 - phosphmedehydrogenase , g6pd )活性的影響,結果表明so _ 2吸入使小鼠不同組織的谷胱甘肽氧化還原系統發生了改變,表現為隨著so _ 2吸入濃度的增加,該系統中的抗氧化酶活性的顯著變化和抗氧化物質水平的顯著降低,且存在著組織差異性。In order to get some functional clues from their structures, the upstream regulation region of ndrgl gene and second structure of ndrg2 protein are performed bioinformatics analysis ; we found that there are several binding sequences of some diffirent transcription factors, their functions include regulating tissue - specific gene expression, regulating expression of genes related to growth and early development of cells, besides this, regulating expression of genes under some stimulated conditions, and so on. predict in protein fold classification shows that ndrg2 belongs to alpha / beta hydrolase fold family, and there are high similarity between ndrg2 and epoxide hydrolase from bacteria, this suggests that ndrg2 protein may has enzymatic functions associated with resisting the oxidative stress, maintaining the balance of cell redox potential, involving in the metabolism process of xenobiotics or intracellular toxic molecules
研究發現呷基因的調控區存在多種轉錄因子結合位點,功能主要涉及組織特異性表達調控,細胞生長發育相關基因的表達調控,刺激反應基因的表達調控等; ndrgz蛋白在結構上屬于a小水解酶類折疊,折疊分類預測表明ndrg2與其中的的細菌環氧化物水解酶的二級結構極為相似,提示ndrgz蛋白具有一定酶活性,可能參與細胞抗氧化應激反應,維持細, an ) armtbffiofbfochmilsyn ) mdafblechmrbfobo4第四軍醫大學碩士學位論文胞內氧還電勢平衡,參與內外源有毒物質的代謝等。Mpges, an inducible perinuclear enzyme, is preferentially coupled with the inducible cox - 2 to promote delayed pge2 generation. however, the expression and regulation of pges in mammalian uterus during early pregnancy are still unknown
目前有關前列腺素在生殖過程中的調控研究主要集中在環氧合酶方面,關于pges在哺乳動物子宮中的表達和調節還未見報道。分享友人