脫水酶 的英文怎麼說
中文拼音 [tuōshuǐ]
脫水酶
英文
alad-
Both prephenate dehydrogenase and prephenate dehydratase have been isolated from plants.
預苯酸脫氫酶和預苯酸脫水酶都已從植物中分離出來。Changes in desiccation tolerance during imbibition of zea mays l. relate to activity of reactive - oxygen - scavenging enzymes
吸脹玉米種子脫水耐性變化與活性氧清除酶活性的關系4. engineering dhqase ( arod ) - deficient e. coli mutant with a second copy of the arob gene gene targeting technique was used to disrupt the arod gene in e. coli chromosome. the mutant 31bk was engineered, in which homologous recombination of the arobkanr gene cassette into the arod locus ( arod : : arobkanr ) of the e. coli strain atcc31884 genome utilized the helper plasmid pkd46 with red system. the host cell 31bk lacked catalytic activity of dhqase ( arod ) and had a second copy of the arob gene, so it improved carbon flow into the quinic acid biosynthesis direction
構建宿主菌基因精確定位突變株31bk （ arod : : arobkan ~ r ）為了改變代謝途徑脫氫奎尼酸（ dhq ）分支點上的代謝流量，使之充分流向目的產物奎尼酸合成方向，利用基因打靶技術構建了31884宿主菌arod基因精確定位插入突變體，使dhq脫水酶（ dhqase ）失活，阻斷了碳代謝流流向芳香氨基酸生成的方向，同時用同源重組的方法將arob基因定位整合入染色體上，解除了限速酶對碳代謝流通過共同途徑到達dhq的阻遏影響，並減輕代謝負擔。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Fetal unilateral cleft lip and palate : detection of enzymic anomalies in the amniotic fluid. raposio e, panarese p, santi pl palst reconstr surg, 1999 ; 103 ( 2 ) : 391 - 394
檢測315例正常孕婦羊水中乳酸脫氫酶和肌酸磷酸酶水平，發現胎兒患單側唇齶裂者（ 3例） ，兩種酶含量顯著升高。認為局部代謝改變與唇齶裂的發生有關。Gc binds to mr with higher affinity than gr. this gc - receptor interaction is also controlled at the pre - receptor level by two important factors : corticosteroid binding globulin ( cbg ) and 11 b - hydroxysteroid dehydrogenases ( 11 - hsds )
糖皮質激素與受體結合的量除與血漿中糖皮質激素水平、皮質醇結合蛋白（ cbg ）濃度有關外，還受到細胞內受體前糖皮質激素代謝酶? 11 -羥基類固醇脫氫酶（ 11 - hsd ）的調節。Gene clone and sequence analysis of glycerol dehydratase
甘油脫水酶結構基因The genetic polymorphism of - aminolevulinic acid dehydratase in uighur and yi population in china
酮戊酸脫水酶基因多態性的分析Chorismate acid is branch point in aromatic amino acids biosynthesis, related to phenylalanine, bifunctional enzymes chorismate mutase / prephenate dehydratase ( encoded by phea ) is rate - limiting enzyme
分支酸是芳香族氨基酸合成途徑的分支點，與苯丙氨酸合成有關，雙功能酶分支酸變位酶-預苯酸脫水酶（ phea基因編碼）是關鍵酶。In consideration of the colinearity between the activities of avermectin pks domains and structure of the polyketide product, the dh2 domain of avermectin pks, which corresponds to c - 22, 23 dehydration, appears to have partial dehydratase activity and this results in a mixture of c - 22, 23 double bonds ( " 1 " components ) and c23 hydroxy compounds ( " 2 " components )
目前國內外尚未見有關僅產阿維菌素b1菌株的報道。根據阿維菌素pks基因結構與其聚酮合成反應步驟之間的線性關系，推測b2組分的產生可能是由於阿維菌素pks模塊2中脫水酶（ dh ）的不完全活性所造成。The protective efficacy on lactobacillus casei shirota of four cryoprotectants, including skim milk, glucose, sodium glutamate and fructose, was studied by viable cell count and lactate dehydrogenase activity analysis of rehydrated starter made by freeze - drying l. casei shirota
摘要將活化后的乾酪乳桿菌代田株製成凍干發酵劑，通過對其復水后活菌數和乳酸脫氫酶的測定，比較了脫脂奶、葡萄糖、谷氨酸鈉、海藻糖4種凍干保護劑對乾酪乳桿菌代田株的保護效果。This paper describes several latest industrial microbial technologies in detail, which are the synthesis of the chiral diols by epoxide hydrolase from microbie, cofactors regeneration for redox with fdh, production of nano / micro wire by the phage display, metabolic network rebuilding for conventional fermentation and the application of the organic solvent tolerance and the metagenomics technology
本文綜述了幾項最新的工業微生物技術，主要包括：微生物環氧化水解酶催化合成手性二醇、微生物甲酸脫氫酶用於再生氧化還原反應的輔因子、通過噬菌體展示技術得到納米級金屬絲、代謝網路改造和重建用於傳統發酵生產以及有機溶劑耐受菌和宏基因組技術的應用。The protection effect of several cryoprotectants on the freeze dried lactobacillus starter was studied by measuring the viable cells ' number and activity of lactate dehydrogenase after the starter was activated in liquid media
摘要通過對不同種類不同濃度的凍干發酵劑復水后活菌數和乳酸脫氫酶的測定，比較了幾種凍干保護劑對瑞士乳桿菌的保護效果。In addition, the well retained stability and integrity of cell membrane of boea leaves might also be an important mechanism which make them resurrect well. by using mrna differential display, 5 desiccation sensitive cdnas, 52 desiccation - induced cdnas, 21 up - regulated cdnas, 14 down - regulated cdnas and 16 phosphate induced cdnas were obtained. the cloning, sequencing, homological blasting and northern blotting results of 5 desiccation - induced cdnas and 3 phosphate induced cdnas implied that signal transduction induced by desiccation, regulatory gene cascades and functional genes such as g protein, protein kinase, vp3 - and mad3 - like genes might be involved in dehydration in the resurrection plant boea hygrometrica
對其中5個脫水特異誘導表達牛耳草光合作廠j的脫水保護和復甦機理的cdna （包括可能與復甦能力有關的cdna ）和3個磷酸鹽處理誘導表達的cdna進行克險測序、同源性探測和northern雜交檢測表明，牛耳草脫水過程中誘導表達的基因可能涉及到脫水脅迫的信號轉導「蛋白、蛋白激酶等） 、調節基因的級聯作用（ vp3 ， mad3樣基因等） 、結構基因產物調節細胞結構（包括細胞質膜）在脫水脅迫中的穩定性等。Electrolyte analysis was consistent with acute tumour lysis syndrome ( atls ) with hyperkalaemia, hyperphosphataemia, hyperuricaemia, hypocalcaemia and elevated serum creatinine and lactate dehydrogenase levels
電解質分析結果符合急性腫瘤細胞溶解綜合征合併高鉀血癥、高磷血癥、低鈣血癥、血肌酐和乳酸脫氫酶水平升高。Interventional effect of lactate dehydrogenase antibody on vasogenic brain edema of rats
乳酸脫氫酶抗體對大鼠血管源性腦水腫的干預效應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。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One is phosphatase - like domain and the other is glycerol - 3 - phosphate dehydrogenase domain. the former domain may catalog the dephosphation of the glycerol - 3 - phosphate and the later presumably synthesize the glycerol - 3 - phosphate according to similarity searching, domain localization and structure comparison. these should give an evidence for the functional research of this gene
通過相似性搜索，結構域定位以及結構比較分析我們認為磷酸化酶結構域很可能是催化3一磷酸甘油水解，而3一磷酸甘油脫氫酶結構域是催化3一磷酸甘油合成的，為這個基因功能的鑒定提供了根據分享友人