核心酶 的英文怎麼說

中文拼音 [héxīn]
核心酶 英文
core enzyme
  • 核 : 核構詞成分。
  • 酶 : 名詞[生物化學] （生物體的細胞產生的有機膠狀物質） enzyme; ferment
  • 核心 : core; kernel; kern; heart; centre; elite; nucleus
  1. Lipoprotein lipase ( lpl ) is a critical enzyme of catabolic metabolism in lipoproteins, its major function is the hydrolysis of the core triglycerides of circulating chylomicrons and very low density lipoproteins

    脂蛋白脂肪酶是脂蛋白分解代謝的關鍵酶，其主要功能是水解cm和vldl這些脂蛋白中的甘油三酯核心。
  2. Abstract : several - aromaticamino ketones, which were designed according to some hypothetical models of the cyclooxygenase and 5 - lipoxygenase active sites, were synthesized by an amino exchange reaction. the structures of the eight new compounds were confirmed by ir, 1h - nmr and elemental analysis. the results of the pharmacological tests showed some of the investigated compounds had significant anti - inflammatory activity on croton oil - induced ear edema of mice

    文摘:根據環氧化酶、 5 -脂氧化酶活性中心結構模型設計了一組-芳胺酮類化合物，並用胺交換反應合成了這些化合物.經紅外光譜、核磁共振氫譜及元素分析證實了8個未見文獻報道的化合物的結構.藥理實驗結果顯示.部分受試化合物在巴豆油誘發小鼠足趾腫脹模型中表現出一定的抗炎活性
  3. Construction of adenoviral vector for luciferase driven by htert core promoter modified with myc - responsive elements

    核心啟動子引導熒光素酶表達的腺病毒載體
  4. Only antibody of e of second liver virus and core antibody two positive, transaminase is normal also, this does not have the requirement of second liver

    僅乙肝病毒e抗體和核心抗體兩項陽性，轉氨酶也正常，這不具備乙肝的條件。
  5. The characteristic of epoxide hydrolase structure and its catalysis performance were described emphatically, i. e. two functional structures : core structure and cap structure, and trinitarian eatalytieal activity conformation

    重點介紹環氧化物水解酶的結構特點和催化特性，即核心結構和帽子結構兩個功能性結構及三位一體的催化活性構象。
  6. The full orp encodes a 487 - amino acid protein with a calculated molecule weight of 53. 484 kda and an isoelectric point of 6. 75. at the primary sequence level, it shared high homology with clr, so was named clr - like serine protease, clsp. the clsp sequence has been submitted to genbank / embl ( genbank accession number af178985 )

    該蛋白在核酸和氨基酸水平上與人補體組分cl :表現高度同源，故將其命名為補體cl :樣絲氨酸蛋白酶（旦lr一like旦erineprotease ， clsp ） ，該基因已經在ge心ank登錄（登錄號為af17s985 ） 。
  7. Its km for sacilin at50 andph5. owas3. 73mg / ml. with the analysis of kinetics, the p - glucosidase showed synergistic action to the endoglucanase and the endoglucanase inhibited the p - glucosidase. the mechanism for their interaction was explained that the endoglucanase was combined with its products and the inhibition of these products to endoglucanase was removed by its hydrolysis by p - glucosidase

    經兩組分共同作用的酶反應動力學分析后發現，兩組分這種相互作用機制的核心是：內切酶和?葡萄糖苷酶與內切酶的水解產物，也是其底物類似物? ?纖維二糖和纖維寡糖的結合以及-葡萄糖苷酶對該產物的水解。
  8. It is a very basic, single - chain protein with molecular weight about 14 kd. it shares 33 % sequence identity with bovine pancreatic rnasea and has structurally equivalent counterparts for the two histidines and one lysine that comprise the catalytic residues for ribonucleolytic activity

    它是由123個氨基酸組成的分子量約為14kd的單鏈堿性蛋白質，與牛胰核糖核酸酶有33的同源性，兩個組氨酸和一個賴氨酸殘基組成了血管生成素核糖核酸酶活性中心。
  9. In this study, it has been put forward that taking reactive nanometer magnetic fe304 particles as magnetic nucleus, and the copolymer of styrene ( st ) ? crylic acid ( aa ) as macromolecular shell, we could synthesize, magnetic polymer composite microspheres containing carboxyl groups on their surface, then microspheres are activated by thionylchloride, the surface of such magnetic composite microspheres thus produced had reactive acid chloride groups which then react with the free amino groups of the free soluble enzymes to give peptide bonds ( ? o ? h ?,

    本研究首次提出了以納米級磁性fe _ 3o _ 4粒子為核心，苯乙烯（ st ） ?丙烯酸（ aa ）共聚物為高分子殼層，合成了表面帶羧基的磁性高分子復合微球，然後將這種微球用二氯亞碸進行活化處理，在其表面形成了反應性酰氯基團，該基團可以與游離酶的氨基形成肽鍵，從而將游離酶固定化。
  10. Immobilized cells are the core of the enzyme engineering, which advance the enzyme technology level

    摘要固定化細胞技術是酶工程的核心技術之一，它將酶工程提高到一個新水平。
  11. Modern biotechnology, represented by gene engineering, cell engineering, enzyme engineering, fermentation engineering and protein engineering, is the forefront for scientific innovation in the 21st century. developing ? iological technique and its relevant industry vigorously has become the core of investment and keystone in economic strategy of many countries around the world. a series of preferential policies and regulations have been set down in order to foster and encourage its development

    以基因工程、細胞工程、酶工程、發酵工程和蛋白質工程技術為代表的現代生物技術是21世紀世界科技創新的前沿，大力發展生物技術及其產業已成為各國投資發展的核心產業及經濟戰略重點，並制定了一系列優惠的政策和法規，扶植和鼓勵其發展。
  12. 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。
  13. Bbic inhibits proteases, enzymes that play important roles in the inflammation and demyelination processes that are at the heart of ms

    蛋白激酶在炎癥反應和脫髓鞘反應（多發性硬化的核心變化）中起重要作用，而bbic可以抑制蛋白激酶的作用。
  14. In hela cells, by using anti - brgl antibodies, anti - rna polymerase ii antibodies and anti - nfl / ctf antibodies, the core subunit brg1 of baf complex and rna polymerase large subunit were found well immunofluorescently co - localized, while nf1 / ctf and rna polymerase large subunit were poorly co - localized. brg1 and nf1 / ctf were also well co - localized. in order to further reveal the relationships of baf complex with nf1 / ctf and rna polymerase ii large subunit at the ultra - microscopic level, we performed the double - labeling immunoelectron microscopy experiment with hela cells

    以hela細胞為材料，分別用抗brg1抗體、抗rna聚合酶抗體和抗nf1 ctf抗體進行免疫熒光共定位分析，發現baf復合物的核心亞基brg1和rna聚合酶的大亞基存在很好的熒光共定位現象， nf1 ctf和rna聚合酶的大亞基之間的共定位現象不明顯， brg1和nf1 ctf也有很好的共定位現象。
  15. The lhcii, which lies outside, was digested partly in both naci - washed psil particle binding the 33 kd protein and caci2 - washed psil particle lacking the 33 kd protein, independent of binding of 33 kd protein. however, caci2 - washed psil particle was more sensitive to tryptic attack than naci - washed psil particle, especially, cp43 decreased more significantly in caci2 - washed psil particle than in naci - washed psil particle. oxygen - evolving psil core complex was sensitive to trypsin digesting, cp43, d2, d1 and 33 kd protein were digested even under slight trypsin treatment and the fragment were verified by western blotting

    結果顯示：在nacl鹽洗ps顆粒和cacl _ 2處理ps顆粒中， lhc容易被酶解； cacl _ 2處理ps顆粒比nacl鹽洗ps顆粒對胰蛋白酶作用敏感；與nacl鹽洗ps顆粒相比，在除去33kd蛋白后， cacl _ 2處理ps顆粒的cp43更容易被酶解；放氧核心復合物對胰蛋白酶更敏感，在低濃度的胰蛋白酶作用下， cp47不被水解，而cp43 、 d _ 2 、 d _ 1和33kd蛋白被部分水解， western - blotting可以檢測到它們的水解片段。
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