malic enzyme 中文意思是什麼
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The tested isozymes included esterase ( est ) 、 superoxide dismutase ( sod ) 、 malate. dehydrogenase ( mdh ) 、 malic enzyme ( me ) 、 glutamate dehydrogenase ( gdh ) 、 peroxidase ( per ) and alcohol dehydrogenase ( adh ). there were obvious differences between the normal strain and its degenerative strain in est 、 mdh 、 me 、 sod. the zymotype were the same in the other isozymes. the results were not only used to test the degenerative strain at young stage, but also as the theoretical base to study the genetic mechanism of the degenerative strain
而其餘四種酶在正常菌株和退化菌株中酶譜一致。本研究不僅可以作為菌株退化早期鑒別的手段之一，而且為進一步研究菌種退化遺傳機理提供了蛋白質水平上的一些理論依據。 -
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。 -
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。 -
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。 -
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。
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