酰基酰胺酶 的英文怎麼說

中文拼音 [jīàn]
酰基酰胺酶 英文
acylamidase
  • 酰 : 名詞[化學] （酰基） acyl
  • 胺 : 名詞[化學] amine （氨 nh3 分子中部分或全部氫原子被烴基取代而成的有機化合物）
  • 酶 : 名詞[生物化學] （生物體的細胞產生的有機膠狀物質） enzyme; ferment
  1. Abstract : in ureide - transporting legumes ， ureides ( allantoin and allantoic acid ) are major transportform of biological fixed nitrogen. the distribution ， properties ， structure and regulation of plant allantoinase were reviewed in detail. the advances in the recent studies on allantoate amidohydrolase and ureidoglycolate amidohydrolase were introduced. and the works desired to be done were pointed out

    文摘:全面綜述植物酰脲降解代謝酶的研究現況，概述植物尿囊素酶的分佈、性質、結構，以及調節控制，並簡介植物尿囊酸酰胺水解酶和脲基乙醇酸酰胺水解酶的研究近況，同時指出待研究的方向。
  2. First, three isozymic systems ( lactate dehydrogenase ( ldh ), esteraes ( est ), malate dehydrogenase ( mdh ) ) extracted from threepopulations of mandarinfishes were detected by discontinuous vertical plate polyacrylamide gel electrophoresis ( page ). several loci were tested but none polymorphic locus was detected in qiupu river population. the results showed that : ldh can be used as biochemical markers to identify these three populations of mandarinfishes

    首先，本試驗採用聚丙烯酰胺凝膠電泳（ page ）對我省三個水域鱖魚群體3種同工酶（ ldh 、 est 、 mdh ）的不同基因座位進行了檢測，結果表明： ldh同工酶可以作為區分秋浦河鱖魚、長江鱖魚兩個群體與萬佛湖鱖魚群體的生化遺傳標記；其次，運用rapd技術分析了三群體鱖魚的基因組dna的多態性。
  3. Many glycoproteins of lower and higher eucaryotes are attached to the plasma membrane by means of a glycosylphosphatidylinositol ( gpi ). gpi - anchored proteins are synthesized on membrane - bound ribosomes. upon translocation of the pro - protein across the endoplasmic reticulum membrane, gpi : protein transamidase ( gp1t ) recognize and removes the carboxy terminal gpi signal sequence and attaches a gpi molecule to the newly exposed carboxy terminal amino acid

    Gpi化前體蛋白在依附於膜的核糖體上合成，當其易位穿過內質網（ er ）膜后，被gpi ：蛋白質轉酰胺基酶（ gpit ）識別， gpit在移走其羧基端gpi信號序列的同時將gpi分子連接至新生成的氨基酸位點上。
  4. Investigation of antimicrobial resistance and genotypes of extended - spectrum - lactamases - producing gram - negative bacteria isolated from pediatrics in shenyang

    內酰胺酶革蘭陰性菌的耐藥性與基因型研究
  5. The results of lauryl sodium sulfate - polyacrylamide gel electrophoreses ( sds - page ) of the aggregate precipitate and supernatant and the result of high - performance size - exclusion chromatography of the supernatant indicated that, by wrongly linked intermolecular disulfide bonds soluble bi - molecular and tri - molecular egg white lysozyme aggregate could be simultaneously formed except being renatured to native and active egg white lysozymes during the refolding procedure of denatured - reduced egg white lysozyme ; the aggregate precipitate could be further formed by the non - covalent bonds interaction between the soluble hi - molecular egg white lysozyme aggregates, and the soluble tri - molecular egg white lysozyme aggregate could still stay at the supernatant

    沉澱和上清液的不連續十二烷基硫酸鈉聚丙烯酰胺凝膠電泳（ sds - page ）和高效凝膠排阻層析分析結果表明，還原脲變性蛋白溶菌酶在稀釋復性過程中除了能夠復性成天然態蛋白溶菌酶分子外，還會形成可溶的蛋白溶菌酶分子二聚體和三聚體，二聚體和三聚體主要是靠分子間二硫鍵的錯配連接而成的；可溶的蛋白溶菌酶分子二聚體之間通過非共價鍵相互作用而形成集聚體沉澱，而可溶的三聚體溶菌酶分子則仍處于復性液上清液中。
  6. It inhibits the activity of glutamine synthetase ( gs ) which is necessary for the production of glutamine and for ammonia detoxification

    草丁膦除草作用機理是抑制植物的氨基酸生物合成酶?谷氨酰胺合成酶（ gs ） ，使雜草產生氨中毒。
  7. In this thesis, we have done some research on the characterization of cu, zn - sod from hog blood by polyacrylamide gel electrophoresis, electric focusing electrophoresis and dealing with some different reagents

    本文採用聚丙烯酰胺凝膠電泳，巰基已醇- sds -聚丙烯酰胺凝膠電泳，等電聚焦電泳以及各種凝膠層析的方法對豬血銅鋅超氧化物歧化酶進行了研究。
  8. The enzyme of microbial transglutaminase ( mtg ) can modify the structure and properties of proteins through catalyzing an acyl transfer reaction of a - carboxyamide group of glutamine residue in a peptide chain, resulting the cross - linking of proteins

    摘要微生物谷氨酰胺轉胺酶（ mtg ）可通過催化蛋白質谷氨酰胺的酰基轉移反應改變蛋白質的結構和性質，是一種有廣泛應用前景的重要新型酶制劑。
  9. A - l was infected on monolayer sffi ther the third plaque purification to reproduce in quantity and named it a - 2. after a - 2 was infectal on sffi monolayer cell 4d harvested the cpe cell. the analysis results with sds - page and dot - elisa showed that prv vp7 gene was - - o - - abstract expressed in baculovirus

    接種a - 2代病毒于sf9單層細胞上， 4d后收獲病變細胞，通過sds -聚丙烯酰胺凝膠電泳（ sds - page ）和免疫酶斑點技術（ dot - elisa ）分析，表明prv - vp7基因在桿狀病毒表達系統中得到了表達。
  10. The genetic variation of eight isozyme expressed by twelve gene loci among 3 natural populations of picea crassifolia was studied by the aids of page electrophoresis

    摘要採用聚丙烯酰胺凝膠電泳實驗對青海雲杉的3個天然群體（甘肅祁連山、青海大通，甘肅甘南州）的12個基因位點表達的8種同工酶的遺傳變異模式進行了研究。
  11. Study on the molecular epidemiology of shv type - lactamase - encoding genes of multiple - drug - resistant acinetobacter baumannii

    內酰胺酶耐藥基因分子流行病學研究
  12. The isolation of crude cu, zn - sod can be started with organic solvents ( ethanol - chloroform ) in the classical manner. then we take two different methods : the first one is that chromatography is carried out on sephadex g100, g50 at room temperature with ph7. 6, 0

    純化后的兩種樣品經聚丙烯酰胺凝膠電泳鑒定和酶活性測定，結果表明：兩種方法分離純化的sod純度高，活力也高，說明後者在前者的基礎上發展起來后，更趨于合理。
  13. The molecule weight of the 6 - pgadase is 110000da, which is measured by akta fplc and the molecule weight of subunit is 51000da, which is measured by sds - page. therefore one 6 - pgadase has two same subunits

    用sephacryls - 300柱（ aktafplc系統）測得全酶相對分子質量為110000da ，用sds -聚丙烯酰胺凝膠測得電泳亞基相對分子質量為51000da 。
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