磷酸脫氫 的英文怎麼說

中文拼音 [līnsuāntuōqīng]
磷酸脫氫 英文
glucose6phophate dehydrogenasese
  • : 名詞[化學] phosphorus (15號元素,符號p)
  • : 酸構詞成分。
  • : 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] (氣體元素) hydrogen (h)
  • 磷酸 : [無機化學] orthophosphoric acid; phosphoric acid磷酸胺 [化學] phosphamide; ammonium phosphate; 磷...
  1. Glycerol phosphate dehydrogenase

    甘油磷酸脫氫
  2. Cloning and characterization of glyceraldehyde - 3 - phosphate dehydrogenase gene from chaetomium globosum

    磷酸脫氫酶基因克隆及特性分析
  3. From the aspects of agricultural economic and environmental ecological effects, were the effects and mechanism of rare - earth micro - fertilizer to improve the growth, development, quality and yield of the crops ; the adjustment of crops growth by influencing the number of microbial population in soil district and the function of the soil dehydrase, alkaline phosphatase, urease and sucrase ; the ecophysiological effects of alleviating the injure of acid rain, ultraviolet radiation, heavy metal on crops were illustrated ; the sureness of bee ' s use in agricultural was provided, according to the rule of the distribution and enrichment of be in crops

    摘要從農業經濟效應和環境生態效應二方面,論述了稀土肥料促進作物生長、發育,提高作物產量,改善作物品質的效應與機理;影響土壤區系中微生物種群數量和土壤酶、堿性酶、脲酶及蔗糖酶的功能,繼而反饋調節作物生長;緩解雨、紫外輻射和重金屬傷害作物的生態生理學效應;並以稀土在作物體內分佈與富集規律為參考,探討了稀土農用的安全性。
  4. Study of newborn umbilical blood screening of g6pd deficiency

    磷酸脫氫酶缺乏的研究
  5. 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:天冬氨轉氨酶( l個位點, 2個等位基因) ,堿性酶( 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) ,蘋果酶( l個位點, 3個等位基因) ,蘋果酶( l個位點, 2個等位基因) ,乳酶( l個位點, 4個等位基因) ,葡萄糖轉氨酶( l個位點, 3個等位基因) ; a澱粉酶為單態。
  6. 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酶和肌酶水平,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。
  7. Cloning of glycerol - 3 - phophate dehydrogenase gene in dunaliella salina and prediction of its protein structure

    甘油酶基因克隆及其蛋白質結構預測
  8. 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3一甘油酶基因核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,化酶結構域和3一甘油酶結構域。
  9. The alga regulates its inside turgor to adapt the outside osmotic change by synthesizing a large amount of glycerol. it is important to study glycerol - 3 - phosphate dehydrogenase, the key enzyme of the glycerol metabolism to know how the species can sustain the hyperosmotics press by accumulating so much glycerol

    該藻通過甘油進行細胞膨壓的調節,因此對甘油合成途徑上的關鍵酶3 -甘油酶( glycerol - 3 - phosphatedehydrogenase ,簡稱為gpdh )的研究是至關重要的。
  10. 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;土壤酶、脲酶、酶活性的下降幅度較為明顯,過氧化酶、蔗糖酶活性次之,蛋白酶活性較為穩定。
  11. 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、高血癥、低鈣血癥、血肌酐和乳酶水平升高。
  12. 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、蘋果酶、葡萄糖異構酶、蘋果酶和過氧化酶等同工酶進行了分析比較。
  13. It ' s pi is 5. 2 as determined with ief. amino acid composition analysis showed that one subunit of 6 - phosphogluconate dehydrogenase has about 480 amino acids and there are plentiful of ala, asp, leu, ser, glu, thr, phe, lys in it

    氨基組成分析表明:枯草芽孢桿菌6 -葡萄糖酶的亞基由約480個氨基殘基組成,富含丙氨、門冬氨、亮氨、絲氨、谷氨、蘇氨、苯丙氨、賴氨
  14. 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。
  15. 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主要脂質脂酰膽堿( pc )合成量; rt - pcr擴增檢測肺組織中pc合成限速酶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。
  16. 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化酶結構域很可能是催化3一甘油水解,而3一甘油酶結構域是催化3一甘油合成的,為這個基因功能的鑒定提供了根據
  17. A large scale dna sequencing of the random clone in the library was performed. est of glycerol - 3 - phosphate dehydrogenase gene was gained and the full - length cdna of glycerol - 3 - phosphate dehydrogenase gene then was achieved as following described. first the 3 " coding sequence and 3 ' utr glycerol - 3 - phosphate dehydrogenase gene was sequenced according to subclonin g the pgpdh - 3 plasmid

    然後在對文庫隨機克隆進行測序的同時,運用生物信息學手段尋找到3 -甘油酶基因的序列表達標簽( est )序列,在這個基礎上對3 -甘油酶全長基因進行了克隆。
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