脫磷酸化酶 的英文怎麼說
中文拼音 [tuōlīnsuānhuà]
脫磷酸化酶
英文
dephosphorylase-
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。The stations e2 and 1 - 4 were located at the cold water mass area of the central yellow sea, which characterized by low temperature, high salinity and stable theromocline would generate a retention mechanism that promoted the formation of separate, self - supporting stocks of krill. 2 genetic diversity and differentiation of p. latifrons specimens of p. latifrons were collected from the east china sea and the south china sea. the zymogram phenotypes of aspartate aminotransferase ( e. c. 2. 6. 1. 1, aat ), alkaline phosphatase ( e. c. 3. 1. 3. 1, alp ), a - amylase ( a - amy ), r - amylase ( r - amy ), esterase ( est ), lactate dehydrogenase ( ldh ), raalate dehydrogenase ( mdh ), malic enzyme ( me ), and phosphoglweoisomerase ( pgi ) were scored
（二）寬額假磷蝦遺傳多樣性和遺傳分化研究1 .本文對東海外海和南海2個站位寬額假磷蝦群體進行了分析，在檢測的9個酶系統中，共檢測到11個酶位點:天冬氨酸轉氨酶（ l個位點， 2個等位基因） ，堿性磷酸酶（ 2個位點， a加了和a加2各有2個等位基因） ， r澱粉酶（ l個位點， 2個等位基因） ，醋酶（ 2個位點， es巧和est7各有2個等位基因） ，蘋果酸脫氫酶（ l個位點， 3個等位基因） ，蘋果酸酶（ l個位點， 2個等位基因） ，乳酸脫氫酶（ l個位點， 4個等位基因） ，磷酸葡萄糖轉氨酶（ l個位點， 3個等位基因） ; a澱粉酶為單態。Oocyte maturation involves the activation of various signal trans - duction pathways that converge to activate maturation - promoting factor ( mpf ) ; this is a key activity that catalyses entry into m - phase of meiosis i and meiosis ii
在爪蟾卵中有大量未被激活的cdc2 - cyclinb復合物，稱為pre - mpf ， pre - mpf在tyr15位脫磷酸變成活性mpf ，起到這個作用的磷酸酶是cdc25 ， cdc25的活性通過磷酸化和細胞位置進行調控。And the intron had a lot of gt repeated sequence. the dna and protein sequence of this gene was analyzed using the bioinformatics tools. two functional domains were found in the protein
運用生物信息學手段對3一磷酸甘油脫氫酶基因核酸以及蛋白質序列做出了分析，發現這個基因編碼兩種功能的結構域，磷酸化酶結構域和3一磷酸甘油脫氫酶結構域。Soil microbial biomass carbon, microbial biomass nitrogen, soil basal respiration and metabolic quotient all showed a decreasing trend under more than 15 mg. kg - 1 cadmium or more than 200 mg. kg - 1 lead, respectively. soil dehydrogenase, urease and acid phosphotase activities have a significant decrease, and the activities of soil catalase and invertase taking sencond place, while soil protease activities showed stable state
隨重金屬濃度增加，各指標下降幅度各有差別，其中微生物生物量碳、微生物生物量氮以及基礎呼吸和微生物代謝商隨重金屬濃度增加而明顯下降；土壤脫氫酶、脲酶、酸性磷酸酶活性的下降幅度較為明顯，過氧化氫酶、蔗糖酶活性次之，蛋白酶活性較為穩定。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。Changes of activities of mlck and dephosphatase in different arterial vessels from hypertensive rats
高血壓大鼠不同血管平滑肌肌球蛋白磷酸化和脫磷酸化酶的變化Mpf is a complex that consists of the protein kinase p34cdc2 and the regulatory protein cycli b ; the protein kinase activity of p34cdc2 is strictly dependent on its association with cyclinb. in xenopus laevis eggs the absent of cyclin b, mpf will not be activited
Ca卜活化p34 」擬的機制第一步是結合cycinb ，並且處于磷酸化狀態，即thr14 、 tyrls和tlirl61都處于磷酸化狀態；第二步是cdc25磷酸酶通過是thr14 、 tyr15脫磷酸化而激活p34 」擬。Experiment shows that tpsl gene can endow organism the ability of synthesis trehalose, the dephosphorylation of the trehalose - 6 - phosphate is not special, and it can be replaced by other phosphatases. the tpsl gene from saccharomyces cerevisiae was cloned by pcr amplification
實驗證實tps1基因就可以使生物體獲得產生海藻糖的能力，酵母的海藻糖合成酶復合體中6 -磷酸-海藻糖的脫磷酸化作用是非特異性的，它可由生物體內的其它酯酶所代替。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。Rt - pcr kit was from takara technology co. ltd. the sequence of the primer of pkb are shown below, together with all the sodn and saodn oligodeoxynucleotide were synthesized in takara technology co. ltd. pkb primers ; forward primer 5 ' cga gaa gcc gcg acc caa cac3 ' and reverse primer 5atg cac tac cgc cgg a3 "
有絲分裂前， cdcz / cy山b 、組蛋白h ;激酶的活性通過被weel和myt激酶磷酸化cdcz的1卜巧和thr14殘基而抑制。在有絲分裂期mpf可以被cdc25活化，這兩個位點被去磷酸化， cdc25是蛋白水解酶，可以使cdcz的t打巧脫離磷酸化。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