活化氨基酸 的英文怎麼說

中文拼音 [huóhuàānjīsuān]
活化氨基酸 英文
activated amino acid
  • 活 : Ⅰ動詞1 （生存; 有生命） live 2 [書面語]（救活） save （the life of a person）:活人無算 （of a goo...
  • 氨 : 名詞[化學] （氮和氫的化合物） ammonia; hydrogen nitride
  • 酸 : 酸構詞成分。
  • 活化 : [化學] activation radioactivation; activate活化處理 activating treatment; 活化分析 [核物理] activ...
  • 氨基酸 : amino acid; gamma-aminobutyric acid （gaba）
  • 氨基 : amido group
  1. Vera is a plant grows in the area of intertropical desert, which contains natural vitamin, mineral, protein active enzyme and lots of amino acid

    美國富恩堂蘆薈採用純天然蘆薈凝乾粉精製而成。米黃蘆薈富含天然維生素、礦物質、蛋白質活性酶及多種氨基酸。對慢性胃炎，消化不良，慢性便秘，腸炎等療效顯著。
  2. The length of this phytase gene is1506bp interrupted once by an intron of 102bp in the 5 " part of the gene, this intron contains donor sequence - gtatgc, lariat sequence - gctgac and acceptor sequence - cag which are typically conserved sequence of the intron of fungal phytase gene. this gene encodes a peptide of 467amino acid residues with molecular weight of 51. 37kda, containing 13 potential n - glycosylation sites and a signal peptide sequence made up of 19 amino acid residues at n teminal of the peptide

    核苷酸序列分析表明， pcr擴增產物中包含有完整的phya基因，該基因全長1506bp ，其中包含一段長102bp的內含子，該內含子具有真菌植酸酶基因內含子的特徵保守序列： donor序列? gtatgc ， lariat序列? gctgac及acceptor序列? cag 。該基因編碼467個氨基酸，理論分子量為51 . 37kda ，其上有13個潛在的n -糖基化位點， n端19個氨基酸為信號肽序列，植酸酶活性位點序列（ crvtfaqvlsrhgaryptdskgk ）位於氨基酸序列的+ 71 + 93 。
  3. Epidermal growth factor ( eof ), a single - chain polypeptide of 53 - amino acid, which was firstly isolated from the submaxillary gland of mice in 1962, has wide potent applications

    人表皮生長因子（ hegf ）是從人尿中提取的由53個氨基酸組成的小分子活性多肽，是促進細胞增殖和分化至關重要的生長因子。
  4. The most commonly used method for the covalent binding of biomolecules onto 1 - d nanostructures is through the diimide - activated amidation of carboxylic acid terminated nanostructures

    最常用的方法是通過端羧酸基納米結構的二酰亞胺活化氨基化合物來進行生物分子與1 - d納米結構的共價結合。
  5. The a - transglucosidase was selectively modified by pcmb, me, edc, clac, acetyl acetone and nbs, and changes in the activities of the enzyme have been detected. the reaction of a - transglucosidase with pcmb, me, edc and clac resulted in a strong inhibition of the enzyme activities which decreased with the increase of modifier concentration. the acetyl acetone and nbs were found without inhibition effect

    酚丙酮、小涅代唬拍酷亞胺剛b引等化學修飾劑對a葡萄糖轉苦酶的幾種氨基酸殘基進行選擇修飾，並測定其酶活力變化，結果表明： pcmb 、 me 、 edc 、 ciac能顯著抑制酶的活性，活力的下降與修飾劑的濃度有關，乙酚丙酮、 nbs白巾飾對酶的奪製作用不明顯。
  6. In thl1 gene, there are some famililar enzyme digest sites including bamh i, hind, sac i and sal i. the sequence of thl1l from brassica oleracea l. shows 99 % identity to the sequence of thll from brassica napus l. there are some phosphorylation sites and an active site of thoiredoxin h members consisting of cppc in thll protein

    甘藍和油菜thl1基因序列有5個堿基的差異，而氨基酸僅有2個氨基酸的變異，同源性達99 。在thl1蛋白的氨基酸序列中發現了一個硫氧還蛋白家族的活性位點（ cppc ）和多個磷酸化位點。
  7. Thioredoxins, an ubiquitous small proteins with a redox active disulfide bridge in its conserved motif - cp ( g ) pc -, are universally distributed in eucaryote and procaryote and have a molecular mass of approximately 12kda. by its disulfide / dithiol interchange reaction, this protein can transmit the regulatory signals to seleted targets ( enzymes, transcription factors etc ) and plays an important role in many plant physiological processes that includes photosynthesis, dna synthesis, transcription, protein disulfide reduction, protein repair, filamentous phage assembly, cell apoptosis and seeds germinating and so on

    該蛋白質中含有保守的- cp （ g ） pc -氨基酸活性基序，該基序中的兩個半胱氨酸殘基可通過巰基二硫鍵的轉換實現其氧化還原狀態的變化和電子氫的傳遞，對細胞中與氧化還原相關的多種生理過程的調節起重要作用。通過同許多酶類、蛋白類、細胞內活性因子相藕連， trx能對光合作用、 dna復制、基因轉錄、細胞凋亡和生長、噬菌體組裝、蛋白質的還原和修復信號傳導等生理過程產生影響和調節。
  8. Functions : this product contains “ antifungal active protein ” with optimal and strong sterilization effect, which could strengthen the immunity of body fluid, activate the macrophage, strengthen the phagocytosis ability of macrophage, strengthen the body immunity, restrain the growth, pervasion and transfer of abnormal cells, the product has strong sterilization effect and could strengthen the disease resistance ; it is remarkably effective in improving the immunity and improving the infirm constitution of pets ; the amino acid content and composition in the product are moderate and rational, with the characteristics of strong palatability, nutrition balance and immune element abundance, etc

    功能：本產品中擁有極佳強烈殺菌作用的「抗菌活性蛋白」 ，能增強體液免疫功能，活化巨噬細胞，增強其吞噬能力，可增強機體免疫力，抑制非正常細胞生長、擴散和轉移，具有強烈的殺毒作用，增強抗病性；對提高寵物免疫力，改善虛弱體質有顯著效果；其中氨基酸含量適中、組成合理，具有適口性強、營養均衡和免疫物質豐富等特點。
  9. Live gene sdb of conten factor, horniness egg whiteaminoacids, vitamin e etc. nourishment essence, can high speed of infiltration hair, from inside to outsideto outside arouse thelive hair the buildup the cell, and change to come to suffer thehair two times life deep into the deep place of hair quality, complement water with nutrient, enhance the horniness, and make the soft piece of hair the bright, alive with luster and flexibility

    內含活性基因sdb因子，角質蛋白、氨基酸維他命e等營養精華，能迅速的滲入發芯，從內到外激活頭發組織細胞，喚醒受損頭發的二次生命，深入發質深處，補充水份和養份強化角質，使頭發柔軟亮麗，充滿彈性和光澤。
  10. The hwtx - i gene was chemically synthesized according to its known cdna sequence, the gene was inserted into vector ppic9k which contained aoxj promotor and the sequence of a secreting signal peptide - a - factor, the cloning ppic9k / hwtx - i was constructed and confirmed by two - step pcr and dna sequence analysis, then it was transformed into host strain gs115, a his + muts cell line was screened and multicopy transformants were screened by various g418 concentrations, the multicopy transformant was named gh1. gh1 was cultivated in flasks. after 6 days of induction by 0. 5 % methanol, the supernatant was checked by 16. 5 % tricine - sds page, which showed there was a band in the position of 3. 5 - 6. 1kd, then it was isolated and desalted by ultrofiltration followed by ion exchange of cm column, after reverse phase hplc of ci8 and vacuum drying, the purified rhwtx - 1 was obtained which was proved to be correct recombinant hwtx - i by tricine sds - page, maldi - tof mass spectrometry, amino acid composition analysis, the n - terminal amino acid sequence and its biological activity, the final field of the purified rhwtx - i was about 80mg / l, accounting for 23. 6 % of it total secretory proteins

    將帶有hwtx -基因的ppic9k經blgii線性化后，轉化酵母宿主菌gs115原生質體后經篩選陽性克隆並經表型鑒定為his ~ + mut ~ s酵母菌，進一步用遺傳毒素g418篩選多拷貝的轉化菌株，命名為gh1 ；將gh1甲醇酵母菌用0 . 5的甲醇誘導表達，發酵上清經90飽和度的（ nh _ 4 ） _ 2so _ 4沉澱， yw - 3 （ mwc03000 ）的超濾膜超濾，再經cm陽離子交換， c _ （ 18 ）反相hplc純化得到分子量為4kd左右的組分，其中4289 . 05的組分經質譜鑒定，氨基酸組成分析和序列測定為正確的表達產物，生物學活性表明其活性為天然毒素活性70 % ，表達量為80mg / l 。
  11. When both genes were co - expressed in e. coli, the activity of ppsa varied from 2. 1 - 9. 1 fold comparing to control, but the activity of tkta was relatively stable ( 3. 9 - 4. 5 fold ). whatever the two genes were expressed respectively or cooperatively, both could promote the production of dahp, the first intermediate of the common aromatic pathway, but co - expression was more effective on forming dahp and screened ppt - and ptp - as more effective. the results demonstrate that co - expression of ppsa and tkta can improve the production of dahp, and what ' s more, when multigenes co - expressed, the recombinant which has coordinated enzymes activity is optimum

    莽草酸途徑的最優化和整體調控基因csra的敲除正是上述改變的分子基礎，同時也為三種芳香族氨基酸的基因工程菌的構建打下了基礎; 7 .在國內外首次實現了共同途徑限制性底物關鍵酶ppsa刁無『及arog與分支途徑關鍵酶基因phea的串聯高效表達，所構建的重組質粒ptga ，其ppsa 、 tkta 、 arog 、 cm和pd的酶活分別比對照提高了3 、 2 、 2 ， 5 、 4 、 2 . 3倍，且其酶活比較協調一致; 8 .將ptga導入到篩選的基因敲除和基因替換菌株大腸桿菌31884 c甲b中，搖瓶發酵證實比以往所構建的基因工程菌株具有較高的phe產量和糖轉化率率，分別為0 . 448 %和22 . 4 % 。
  12. There are active correlation between protein content and the growth stage of teleogryllus derelictus gorochov during its larvae and adult peiod. there are active correlation between the content of amino acids except cystine during larvae period. there are active correlation between the content of fat, total fatty acid, palmitoleic acid, oleic acid, ve2, vc and the activity of catalase and the total growth stage of it

    蛋白質含量在若蟲和成蟲期與發育階段呈正相關，除胱氨酸外17種氨基酸含量在若蟲期與發育階段呈正相關，脂肪、脂肪酸、脂肪酸中軟脂酸和油酸、 v _ （ b2 ） 、 v _ c的含量及過氧化氫酶活力與發育階段呈正相關。
  13. The key stage of fabricating gene chip is pretreatment of glass surface including the processes of nh3h2o treatment, aminosilane treatment and aldehyde treatment. the pretreatment can grow active group that can bind probe effectively on the surface of glass slide. as a result, the actively treated glass slide can suit for fabricating in - situ synthesis high density gene chips

    基因晶元制備技術的關鍵步驟是玻片表面預處理，即對玻片表面進行羥基化、氨基化和醛基化處理，使表面生長的活性基團能有效固定寡核苷酸探針，以滿足原位合成高密度基因晶元對玻片的要求。
  14. A method was developed for the determination of free amino acids in tobacco of different areas ( yunnan, guizhou and henan ) and of different technological processes using reversed phase high performance liquid chromatography ( rp hplc )

    摘要選取雲南、貴州、河南的經不同工藝處理生絲、薄板乾燥、高溫氣流乾燥的煙絲；採用微波協助萃取技術進行樣品的前處理；經活化的陽離子交換柱進行純化，再用柱前衍生反相高效液相色譜的方法對其游離態氨基酸進行含量分析。
  15. Polymerization of the cdi - activated acidic and basic amino acids efficiently enhanced by na and ci

    活化的酸性及堿性氨基酸聚合反應的高效促進效應
  16. There is no characteristic in the amino acid sequence 63 - 152 and it is the piece that we want to delete to identify the function of the segment. ie180 gene mutants deleted the 64 - 151 amino acid was amplified by muti - pcr and were cloned by pmdist - vector. the clone plasmids were named pjmp1p3p2. the segment corresponding to the sequence of 1 - 1079 amino acid of the genbank sequence amplified by pcr, its clone plasmids was named pjmp1p2. the segment corresponding to the sequence of 454 - 1079 of genbank sequence amplified by pcr and its clone plasmids is named pjmp6p2 - three clone plasmids and pcdna3 were digested by restriction enzyme bamhi and hind, the gene segment of p1p2, p1p3p2, p6p2 were recycled

    本試驗應用dnamis及prosis軟體分別對genbank中登記號為no352564的ie180序列進行了蛋白質序列分析，結果表明其1 - 34段氨基酸序列具有典型helix - turn - helix特徵序列，並且富含酸性氨基酸d及e ，是典型的dna識別序列；富含絲氨酸序列的152 - 409氨基酸序列是一個與激活有關的、潛在的磷酸化位點； 454 - 696氨基酸區域是dna結合域； 64 - 151氨基酸片段沒有明顯的序列特徵；從中可看出ie180蛋白的1 - 1080氨基酸段具有典型的轉錄激活因子結構特徵。
  17. The deduced 3 amino acid residues, d32, h64, and s221, were identical with 3 essential amino acids in the catalytic center of protease

    成熟蛋白酶全長275個氨基酸殘基，其中， d32 ， h64 ，和52213個氨基酸殘基為催化活性中心。
  18. Lymphotoxin ( lt ) is a kind of pleiotropic lymphocyte - secreted cytokine which mediates a large variety of inflammatory, immunostimulatory, and antiviral responses. in order to increase the antitumor activity of lymphotoxin and reduce its side effects, the recombinant plasmid pet36b - lt 27 was constructed to express soluble fusion protein cbd - lt 27. the active form of lt 27 could be collected directly with several simple steps by three kind of components on the expressed fusion protein

    本研究通過構建表達n端缺失27個氨基酸的淋巴毒素融合蛋白的重組質粒，在大腸桿菌中實現融合蛋白的可溶及分泌表達，同時利用表達載體上的幾種特殊序列經簡單的分離純化步驟直接獲得大量的有生物活性的淋巴毒素缺失體lt 27 ，為尋找一種高抗腫瘤活性、低臨床毒副作用的生物抗癌藥物進行了有效的探索。
  19. The biological activity of purified lt 27 was tested with the assay system, and its biological activity was 2 - 3 107 iu / mg. pro. the cytotoxicity of purified lt 27 was in the same level with rhtnfp and lt international standard. it shows that lt deletion could keep its high cytotoxicity towards tumour cell l929 in vitro after 27 amino acids deleted from its n - terminal

    用建立的淋巴毒素生物活性測定方法對上述純化的淋巴毒素缺失體lt 27的生物活性進行檢測，測得其比活為2一3xl口iu / mg . proo純化的淋巴毒素缺失體lt 27的生物活性與rhtnfp和淋巴毒素國標標準品的生物活性大致相當，表明lt經n端缺失27個氨基酸后仍能保持很高的體外腫瘤細胞毒活性。
  20. In bioconversion of a d - amino acid and its derivative, the substrate, 5 ' - monosubstituted hydantoin is firstly transferred into an intermediate, d - carbamyl amino acid by d - hydantoinase, and in turn into an optically active d - amino acid by either d - carbamoylase or chemical, nano2. nowadays, the bioconversion of d - amino acids has been industrialized by enzymes, so called one - step process

    D -型氨基酸及其衍生物的生物轉化，經歷兩個反應歷程，首先是在海因酶的作用下，催化5 -單替代海因形成氨甲酰類氨基酸中間物，後者再在酶或化學的作用下，生成相應的光學活性氨基酸或其衍生物。
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