蘋果酸酶 的英文怎麼說

中文拼音 [pínguǒsuān]
蘋果酸酶 英文
malate dehyrogenase
  • 蘋 : no data
  • 果 : Ⅰ名詞1 （果子） fruit 2 （事情的結局; 結果） result ; consequence 3 （姓氏） a surname Ⅱ動詞（吃...
  • 酸 : 酸構詞成分。
  • 酶 : 名詞[生物化學] （生物體的細胞產生的有機膠狀物質） enzyme; ferment
  • 蘋果 : apple蘋果醬 apple jam; 蘋果蜜 apple honey; 蘋果泥 apple butter; 蘋果去皮機 apple peeler; 蘋果肉 a...
  1. For example, fumarase catalyzes the interconversion of malic acid and fumaric acid

    如延胡羧酸酶能催化蘋果酸和反丁烯二酸的可逆反應。
  2. Fruit and vegetable juices. enzymatic determination of l - matic acid l - malate content. nadh spectrometric method

    水果和蔬菜汁. l -蘋果酸含量的酶催化的測定. nadh光譜法
  3. Method for enzymatic determination of l - malic acid l - malate content of fruit and vegetable juices - nadh spectrometric method

    果汁和蔬菜汁中l -蘋果酸的酶催化測定法. nadh光譜法
  4. Fruit and vegetable juices - enzymatic determination of l - malic acid l - malate content - nadh spectrometric method ; german version en 1138 : 1994

    水果和蔬菜汁. l蘋果酸含量的酶性測定. nadn光譜測定
  5. We present a preliminary study on the zymograms of esterase ( est ), lactate dehydrogenase ( ldh ), malate dehydrogenase ( mdh ) from four groups of microtus fortis by vertical discontinous polyacrylamide gel electrophoresis method. the number, mobility and dye intensity of the enzyme band were analyzed

    採用垂直板不連續聚丙烯酰胺凝膠電泳法對四類東方田鼠的酯酶（ est ） 、蘋果酸脫氫酶（ mdh ）和乳酸脫氫酶（ ldh ）進行了初步研究。
  6. Fruit and vegetable juices. enzymatic determination of d - malic acid content. nad spectrometric method

    水果和蔬菜汁. d -蘋果酸含量酶催的測定. nad光譜法
  7. Fruit and vegetable juices - enzymatic determination of d - malic acid content - nad spectrometric method

    水果汁和蔬菜汁. d -蘋果酸含量的酶測定. nad分光光度方法
  8. We have tested 6 allozymic systems, they are per, cyt, sod, es, amy and mdh. there are totally 42 allozymic bands with 15 loci of which 12 are polymorphic and 3 are monomorphic

    檢測了6個酶系統，它們是：過氧化物酶、細胞色素氧化酶、超氧化物歧化酶、酯酶、澱粉酶、蘋果酸脫氫酶。
  9. The results showed : protamine could inhibit the growth of " bacillus subtilis " without destroying the cellular wall and significantly inhibit the activities of succinate dehydrogenase and malata dehydrogenase

    試驗結果表明：鯉魚魚精蛋白對枯草芽袍桿菌具有較強的抑制作用，但對枯草芽抱桿菌細胞壁不產生破壞作用；對黑曲?胞內的琥珀酸脫氫酶和蘋果酸脫氫酶的活性具有明顯的抑制作用。
  10. In order to investigate the antibacterial mechanism of protamine, the effect of protamine on the growth of " bacillus subtilis " and the activities of succinate dehydrogenase ( sdh ) and malata dehydrogenase ( mdh ) in cells of " aspergillus niger " was studied

    通過鯉魚魚精蛋白對枯草芽抱桿菌生長的影響及對黑曲?胞內的琥珀酸脫氫酶（ sdh ）和蘋果酸脫氫酶（ mdh ）活性影響的研究，探討鯉魚魚精蛋白的抑菌機理。
  11. Second round pcr products were cloned to t / a plasmid vectors to set up the subtractive library

    Westernblot分析了nadp一蘋果酸酶蛋白合成隨鹽脅迫的變化情況。
  12. 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。
  13. Random analysis of 13 clones with enzyme restriction showed that 10 plasmids in the clones contained 300 - 600 bp inserts

    胭p二:廠。施二中nadp一蘋果酸酶活性高的多。
  14. After screening, we had identified ten candidate clones which are differentially expressed at salt - treated leaves of aloe vera l. sequence analysis was performed for three clones. one of them scored perfect to already known nadp - malic enzyme gene

    這些表明，鹽脅迫可以誘導這兩種蘆薈中的nadp一蘋果酸酶基因的表達和nadp一蘋果酸酶蛋白的積累，但是誘導的強度與蘆薈品種的耐鹽程度有關。
  15. 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。
  16. After the screening, the expression and identity of the gene for nadp - malic enzyme in leaves of aloe vera l. under salt stress had been done. methods : construction and screening of the subtractive library : to construct a cdna subtractive library of aloe vera l. under salt stress, the leaves of aloe vera l were removed from the seedlings which were treated with 300 mm nacl. suppression subtractive hybridization ( ssh ) was carried out and a subtractive library was constructed

    鹽脅迫下庫拉索蘆薈葉子中nadp -蘋果酸酶基因的表達鑒定：為了檢測蘆薈鹽脅迫下庫拉索蘆薈cdna消減又庫的構建篩選及nadp一蘋果酸酶基因的鹽誘導表達中nadp一蘋果酸酶基因『刀叻心）的表達和nadp一蘋果酸酶（ nadp一ma1ieenzyme ）蛋白的積累是否受著高鹽的誘導，我們利用耐鹽品種庫拉索蘆薈（ a了口。
  17. The main differences in sod exist in two stages - 6 - from darkly - pigmented eye to hatching, which showed two more bands ( sodl " and sod2 " ) in the isozyme pattern of embryo activated by heterogeneous sperm than that activated by homogenous sperm. meanwhile, the other two isozymes ( est and me ) detected in this paper did not show apparent differences between the embryo activated by homogenous sperm and that activated by heterogeneous sperm

    對異精激發彭澤鯽雌核發育子代及其母本彭澤鯽和父本海鯉的血清、肌肉蛋白以及心、肝、腎、腦、眼等組織的酯酶（ est ） 、蘋果酸脫氫酶（ mdh ） 、蘋果酸酶（ me ） 、超氧化物歧化酶（ sod ）和乳酸脫氫酶（ ldh ）電泳圖譜的比較研究。
  18. Expression and identity of the gene for nadp - malic enzyme in leaves of aloe vera l under salt stress : to investigate whether the expression of nadp - me gene and the accumulation of nadp - me protein induced by salt treatment are related to salt tolerance in the aloe plant, northern blot analysis was performed and the activity of nadp - me protein was measured in a tolerant aloe, aloe vera l, and a sensitive aloe, aloe saponarea haw under salt stress

    對其中的3個進行單向測序。其中一個序列在genbank中登錄，獲得的序列號為no . ay179511 . 2 .鹽處理12個小時后nadp一蘋果酸酶mrna誘導增加，且兩種蘆薈中的表達量都在48 ， j 、時后達到高峰。但是其表達水平是不相同的， a了。
  19. Tester cdnas were divided into two groups and ligated to the specific adaptor 1 and adaptor 2r, and then hybridized with normal aloe vera l cdna twice with two rounds of suppression pcr

    同樣用northernblotting對幾種脅迫條件下，庫拉索蘆薈nadp一蘋果酸酶基因a叻貿的表達情況進行了分析。
  20. To further confirm whether the synthesis of nadp - me protein was induced with hours of treatment, western blot analysis of the samples was conducted

    如此相類似， nadp一蘋果酸酶活性在鹽處理12小時后開始誘導增加，活性穩步增加至72小時。
分享友人
分享到 Line

分享到臉書