青酶 的英文怎麼說

中文拼音 [qīng]
青酶 英文
greengage
  • 青 : Ⅰ形容詞1 （藍色或綠色） blue or green 2 （黑色） black : 青布 black cloth; 青牛 black ox3 （年輕...
  • 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. E. coli xl1 - blue cells were tansformed by psurfpga and phages were rescued by m13ko7 helper phage particles. results showed that the heterodimeric enzyme was expressed as a fusion protein that matures to an active biocatalyst connected to the coat protein of phage fd

    以構建的噬菌粒psurfpga轉化具有琥珀突變的大腸桿菌xl1 - blue ，以輔助噬菌體m13k07超感染，進行青霉素g酰化酶基因的表達和在噬菌體表面的展示。
  2. G - banding the gtg banding ( g - banding ) was carried out by the standard trypsin method with slight modification, which works well for protochordate because a good number of reproducible g - bands are consistently obtained from the embryonic cells of late blastulae and early gastrulae of amphioxus b. belcheri tsingtauense

    G帶型用稍作修改的標準的胰酶顯帶技術，進行gtg帶紋的顯示，它們能較好地顯示頭索動物青島文昌魚的晚期囊胚和早期原腸胚的中期染色體的g帶，並且重復性好。
  3. Zhang y, xie q, guo y, et al., a study on adsorption of electrogenerated cystine precipitate onto au electrode using electrochemical quartz crystal impedance system. chinese chem. lett., 1999, 10, 1057

    張友玉，謝青季，袁玉等.溶菌酶在裸金電極和巰基乙酸或正十二硫烷基醇修飾金電極上的吸附.應用化學， 2002 ， 19 ， 4
  4. In this paper, first strand cdna of 3abc gene was synthesized using template rna extracted from cells infected with fmdv. the complete 3abc gene about isoobp was amplified by pcr and ligated into pgem - t easy vector. after transforming e. coli dh5 a, ampicillin resistant colonies were isolated and plasmid dna was prepared and analyzed by restriction analysis and pcr. presence of the full length 3abc gene was verified by nucleotide sequence analysis and the plasmid containing the expected sequence was named as pgem - 3abc. comparing the aquired sequence of 3abc with that of reference strains, the homology is more than 99 percent. the pgem - 3abc was digested with sal i and bgl ii and ligated into xho i and bgl ii - digested expression vector ptriex - 4 neo. lt was identified by restriction analysis and pcr and sequencing that this fragment had a 17bp deletion hi the nucleotide sequence 708bp of 3abc gene, which happened to form a terminator codon behind 3ab gene, but it contained the complete open reading frame ( orf ) of 3ab gene. positive clones were selected and induced with lmmol / l isopropyl - d - galactoside ( iptg ), bacteria were detected by sds - page and western blotting after properly treated. the results showed that the 3ab gene expressed successfully in e. coli and 33. 5ku fusion protein can be recognized by the positive bovine serum of fmdv. the amount of target protein is over 26 % of the total bacteria protein by gel thin layer scanning analysis

    擴增產物連接到pgem - teasy載體中，轉化大腸桿菌dh5菌株，篩選氨芐青霉素抗性菌落，提取質粒經酶切鑒定、 pcr分析以及確證性測序證明，所克隆的1500bp左右的片段含有完整的3abc基因，與國外參考序列相比，同源性在99以上。將重組質粒pgem - 3abc和表達載體ptriex - 4neo分別用sal和bgl與xho和bgl消化后，亞克隆3abc基因至原核表達載體ptriex - 4neo中，通過酶切鑒定、 pcr擴增以及序列分析，發現克隆到ptriex - 4neo載體上的片段於3abc基因708bp處出現了17bp的缺失，碰巧在3ab基因后形成一終止密碼子，但3ab基因的閱讀框架完整，選出含有3ab基因完整閱讀框架的陽性克隆，用iptg誘導表達，收集菌液進行sds - page電泳、 westernblotting分析，結果表明， 3ab基因在大腸桿菌中成功表達，其表達產物為分子量33 . 5ku的融合蛋白，並能被口蹄疫病毒陽性血清識別。經薄層掃描分析，表達量占總蛋白量的26以上。
  5. Study on increasing green pepper juice yield by enzymatic process

    酶法提高青椒出汁率的研究
  6. The extracted marrows ganoderma lucidum and semen zizyphi spinosae contained in threesss can regulate secretion of hydrocortisone in human body and reduce excitation of human body during nighttime ; in addition, ganoderma - lucidum spores and semen zizyphi jointly stimulate secretion of sleeping - inducting peptide in body. improve rate of " high efficient sleeping quality and immunity. recover and strengthen mental strength, mental strength and vigor. through sleeping. the psychlogy and physiology return to the youth level

    「索萊爾」多元明膠囊中所含的靈芝和酸棗仁提取精華，能調節人體內皮質醇的分泌，降低人體在夜間的興奮度；此外靈芝孢子粉和酸棗仁共同作用，能夠在體內刺激「睡眠肽」和格里酶「的分泌，有效促進「高能睡眠」率，延長「高能睡眠」時間，從而達到全面改善睡眠質量，提高免疫力，使體力、腦力、精力得到迅速恢復和加強，通過睡眠將生理及心理狀態調整到青春期水平。
  7. Panipenem and imipenem exhibited comparable in vitro antimicrobial activity, and their activity against gram - negative bacteria such as k. pneumoniae and enterobacter spp was slightly inferior to meropenem, superior to that of ceftazidime, fluroquinolones and - lactam and - lactamase inhibitor combinations

    三種碳青黴烯類抗生素體外抗菌作用優于頭孢他啶、 -內酰胺類抗生素與-內酰胺酶抑制劑合劑、氟喹諾酮類等其它受試藥物。
  8. Considering alcaligenes faecalis pencillin g acylase ( afpga ), which possesses the attractive characteristics for beta - lactam antibiotics conversions, the gene of pga was cloned into two expressing vector pkkfpga and psmlfpga. both the constructed plasmids psmlfpga and pkkfpga contained the pga gene, trc promoter and rrnb transcript terminator, differ in the replicon and antibotic marker, pkkfpga contained multicopy replicon ( cole 1 ) and ampicillin marker. while psmlfpga contained medium - copy replicon ( p15a ) and tetracycline marker

    本文將糞產堿桿菌青霉素g酰化酶（ afpga ）基因構建表達載體pkkfpga和psmlfpga ， pkkfpga和psmlfpga均含trc啟動子、青霉素g酰化酶基因、 rrnb轉錄終止子，其中pkkfpga含有氨卞青霉素抗性基因和cole1高拷貝復制子；而psmlfpga含有四環素抗性基因和p15a中拷貝復制子。
  9. The masp ( mannose - binding lectin - associated serine protease ) gene has been cloned by the method of degenerative pcr and the fragment of the pcr product is 630 bps in length

    本文還利用pcr方法從青島文昌魚基因組dna中克隆masp （甘露聚糖結合凝集素相關絲氨酸蛋白酶）基因片段。
  10. Nitric oxide synthase expression in trabecular meshwork of patients with glaucoma

    青光眼患者小梁網中一氧化氮合酶的表達
  11. Cdna clone and lignite degradation ability of lignin peroxidase from penicillium decumbens p6

    斜臥青黴p6木素過氧化物酶的褐煤降解活性及cdna克隆
  12. The results obtained were as follows : the mic of engineered peptide against staphylococcus aureus atcc 25923 ( penicillin sensitive strain ), atcc 29213 ( penicillinase - producing strain ) and atcc baa - 42 ( methicillin resistant strain ) were 1g / ml, 2g / ml, 4g / nil respectively. pi staining showed the staphylococcus aureus treated with the engineered peptide were dead

    實驗結果表明:該工程多膚對三種atcc標準菌株atcc25923 （青霉素敏感菌株） 、 atcc29213 （產青霉素酶菌株） 、 atccbaa一42 （耐甲氧西林菌株）的mlc分別為1林留血l 、 2林留ml 、 4林創ml 。
  13. Cdna clone and lignite degradation ability of lignin peroxidase from

    斜臥青黴p6木素過氧化物酶的褐煤降解活性及cdna克隆
  14. The result showed that non - enzymatic browning of greengage juice could be inhibited and natural primrose yellow could be kept in the plasming of greengage by adding 0. 2 % ( mass fraction ) sodium erythorbate ; non - enzymatic browning of greengage juice was restrained more remarkably by vacuum concentration than by normal pressure concentration ; the non - enzymatic browning of greengage juice increased and the color darkened with the increase of concentration and processing temperature ; non - enzymatic browning of greengage juice in the storage could be inhibited under the condition of low temperature, and frozen storage was the best store method of greengage concentrated juice

    摘要結果表明：在青梅果打漿時加入質量分數為0 . 2 %的異抗壞血酸鈉，可防止果汁氧化褐變而保持天然淡黃色澤；減壓濃縮較常壓濃縮明顯抑制了非酶褐變的發生；隨著果汁含量和加工溫度的提高，非酶褐變加快，色澤加深；低溫有利於青梅濃縮汁的貯藏，冷凍貯藏是最佳的貯藏條件。
  15. For the first time a 1539bp squalene synthase ( asqs ) cdna was cloned from a high - yield artemisia annua strain 001 by race strategy

    用race方法首次從青蒿中克隆了一個1539bp全長鯊烯合酶cdna 。
  16. Asqs is 70 %, 77 %, 44 % and 39 % identical to squalene synthases from arabidopsis thaliana, tobacco, human and yeast, respectively. the asqs genomic dna has a complex organization containing 14 exons and 13 introns

    青蒿鯊烯合酶氨基酸序列與擬南芥、煙草、人類、酵母鯊烯合酶的一致性分別為70 、 77 、 44 、 39 。
  17. Analysis of the sequence revealed that adda resembled nifs of nitrogen - fixing bacteria and dnda. the entire add gene cluster showed 78 % identity to dnd gene cluster from s. lividans

    同源性比較揭示add基因簇的adda基因與固氮酶基因nifs高度同源， add與變鉛青鏈黴菌dnd核苷酸的同一性為78 。
  18. It was suggested that the gene t13m11. 8 could be the ast candidate gene. this gene was 1432bp long with 6 exons and 5 introns. the putative protein of t13m11. 8 gene was highly homologous to dihydroflavonol 4 - reductase ( dfr ), which was an important enzyme in the anthocyanin biosynthesis pathway

    該基因的dna序列長1432bp ，含有6個外顯子和5個內含子，編碼的蛋白與花青苷生物合成途徑中的二氫黃酮醇4 -還原酶有較高的同源性。
  19. Through screening a lot of mutants with the method of transparent zones and culture filtrate, the best four were obtained with high - yield of stable phb depolymerase, named as 02, 04, 09 and 14

    以青黴（ penicillium . sp ） ds9701為出發菌株，通過紫外線誘變分生孢子，採用透明圈初篩和搖瓶培養復篩的方法，獲得4個能穩定遺傳的phb解聚酶高產菌株。
  20. Based on the known result, the cdna of papain was tried to cloned from total rna of papaya in this study. though the primers were designed according to the cdna of papain, the cdna of ppiv was attained, which was homologous to that of papin. when compared with the papain gene in embl database, the cdna of ppiv reachs 98. 7 % in homology

    木瓜青果乳汁中含有豐富的半胱氨酸類蛋白酶，據已知的研究結果，本研究嘗試從未成熟的木瓜果的總rna中克隆木瓜蛋白酶基因，雖然在rt - pcr時使用引物的是根據木瓜蛋白酶的cdna序列而設計的，但卻得到了與之有67同源性的番木瓜蛋白酶的cdna序列，對其分析表明，該序列與embldatabase中x78056同一段基因序列相比較同源性達98 . 7 。
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