氨基菌素 的英文怎麼說
中文拼音 [ānjījūnsù]
氨基菌素
英文
aminomycetin-
Ammonifiers in suzhou creek can not use inorganic nitrogen and carbamide as nitrogen source ; additional carbon source and garbage lixivium have little influence on ammonifiers growth ; high content of salt and low temperature restrain ammonifiers growth ; alkalescent condition has little influence on ammonifiers, but acidic condition restrain ammonifiers growth ; the biomass of ammonifiers are not necessary correlated with the function of ammonifiers, adding glucose with 1g / l content into the water sample obviously promote the growth and function of ammonifiers. physiological groups of bacteria play significant role in the translation and
蘇州河的氨化菌無法利用無機氮和尿素作為氮源；在營養條件充足時添加額外c源和富含有機物的垃圾浸出液對氨化菌的生長基本無影響；高鹽度和低溫抑制氨化菌生長；堿性條件對氨化菌的生長影響不大，酸性條件對氨化菌生長具有抑制作用；氨化菌生物量的消長與轉氨活性之間不存在必然聯系， 1g / l的葡萄糖對蘇州河水樣中氨化菌的數量和轉氨功能具有明顯的促進作用。Our previous studies showed existence of apoplast cam in the plant cell and cam had many extracellular functions. so it supposed cam may be one of important extracellular polypeptides and trigger the intracellular signal transduction by binding the receptor. in this study, radiolabelled ligand is used to investigate the binding characteristic of cam and a. thaliana protoplasts. and chemical crosslinking is employed to explore binding proteins in the membrane. at first, ( 35 ) ~ s - cam was produced using ( 35 ) ~ s - labeled amino acid mixture in e. coli. sds - page and autoradiograph indicated high - purified, high - specific radioactivity ( 35 ) ~ s - cam was obtained. electrophoresis of ( 35 ) ~ s - cam is the same as that of unlabeled cam with ca ~ ( 2 + ) or egta ; a quatitive of protoplasts was prepared by enzymolysis
首先，用~ （ 35 ） s標記的氨基酸混合物喂養工程菌成功地制備了~ （ 35 ） s標記的擬南芥鈣調素（ ~ （ 35 ） s - cam ） ， ~ （ 35 ） s - cam純度高、放射活度高、 ca ~ （ 2 + ）與egta存在時的電泳行為與未標記cam相同，可作為一種高靈敏性的探針用於進行受體學分析實驗；用擬南芥種子誘導愈傷，通過酶解制備了大量原生質體。All of our products is exported likelactobacillus acidophilus, bidifobacterium longum, lactobacillus paracasei, lactobacillus rhamnosus, tagatose, lnulin, nisin, natamycin, - polylysine, nucleotides mix, adenosine monophosphate, cytidine monophosphate, guanosine monophosphate disodium, uridine monophosphate disodium, calcium inosinate, calcium guanylate, calcium 5 - ribonucleotide, damp, dcmp, dgmp, tmp, deoxyadenosine, 2, 6 - diaminopurine nucleoside, 2, 6 - diaminopurine deoxynucleoside, adenine arabinoside, adenosine triphosphate, uridine triphosphate, guanosine triphosphate, cytidine triphosphate, cytidine diphosphate choline （ citicoline ） to all over the world, if you are interested in our products, please do visit our website, hope there will fullfill your requirement
主營產品有益生菌（嗜酸乳桿菌、長雙歧桿菌、乾酪乳桿菌、鼠李糖乳桿菌） 、塔格糖、菊粉（菊糖） 、乳酸鏈球菌素、納他黴素、 -聚賴氨酸、核苷酸，腺苷酸，胞苷酸，鳥苷酸二鈉，尿苷酸二鈉，肌苷酸，鳥苷酸鈣，核糖核苷酸鈣，脫氧腺苷酸，脫氧胞苷酸，胸苷酸二鈉，脫氧鳥苷酸二鈉，脫氧腺苷， 2 -氨基脫氧腺苷， 2 -氨基腺苷，阿糖腺苷，胞二磷膽堿，腺苷三磷酸，三磷酸尿苷，三磷酸胞苷，三磷酸鳥苷等D - amino acids as unnatural chiral products are important intermediates in the synthesis of products, such as - lactam semisynthetic antibiotics, antiviral agents, artificial sweeteners, pesticide, peptide hormones, and pyrethroids, etc. though bioconversion of d - amino acids using microbial cells has been realized in industrialization for decades, some limited factors hinder the development of d - amino acid production, and ultimately result in shortage of the raw material in the related industrial fields
目前，用微生物菌體轉化生產d -型氨基酸的工藝路線已經產業化，但天然菌體轉化工藝存在一些限制因素，阻礙了d -型氨基酸的擴大生產，導致產品短缺。因此，利用基因工程菌生物轉化d -型氨基酸已成為世界氨基酸產業的新潮流。Effectiveness of a carbamate insecticide mieyawei, and mixtures of mieyawei and abamactin against the leaf miner
氨基甲酸酯殺蟲劑滅蚜威及其與阿維菌素的混配製劑對美洲斑潛蠅的防治效果Toxicity of several insecticides to liriomyza huidobrenisis and its parasitoid, opius sp
氨基甲酸酯類殺蟲劑及其與阿維菌素的混配製劑對美洲斑潛蠅Results bacterium that isolate take blue negative fungus of leather as the core, among them with copper green false form afterbirth fungus and uncle of pneumonia crayresearch as the main fact fungus, leather getring blue in the positive fungus in order to solidify enzyme negative staphylococcus and getting golden yellow staphylococcus comparatively common ; carbon that alkene antimicrobial it able to bears that medicine is minimum in rate, very beginning spore fungus kind, quinoline promise ketoneses plain, can according to medicine results quick as the clinical to use first - selected at glucosides amino sugar
結果分離出的細菌中以革蘭氏陰性菌為主，其中以銅綠假單胞菌和肺炎克雷伯菌為主，革蘭氏陽性菌中以凝固酶陰性葡萄球菌和金黃色葡萄球菌較為常見；碳青黴烯類抗菌藥的耐藥率最低，頭孢菌素類、喹諾酮類、氨基糖苷類可根據藥敏結果作為臨床使用首選藥。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 。Results according to the analysis and determination of imperatorin, carbohydrate components, amino - acid, extracts, ash and water content, the results showed that the harvest period of radix giehniae in october was appropriate, the process of being sliced with skin and dried under the sunshine or in the oven at low temperature after being washed quickly was the best, the effect of fermented bacteria fertilizer was the best and the second was k2so4 compound fertilizer and k2so4 fertilizer, the contents of carbohydrate components and extracts of radix glehniae " baiyintiao " were the highest and the content of imperatorin of radix glehniae " dahongpao1 was the highest, the quality of radix glehniae during blooming or seeds setting period was worse, the quality of radix glehniae planted in hucheng laiyang was better than those planted in anguo hebei and inner mongolia
結果：通過對歐前胡素、糖類成分、氨基酸、浸出物、灰分和水分的分析測定，結果表明：北沙參採收以10月份為宜；藥材加工以趁鮮水洗、帶皮切片曬干或低溫烘乾最佳；追肥以酵素菌高效生物肥效果最好，其次為硫酸鉀復合肥、硫酸鉀；栽培品種「白銀條」的糖類成分和浸出物含量最高，而「大紅袍」的歐前胡素含量最高；當年開花和當年結種的北沙參質量較差；北沙參藥材質量以萊陽胡城產最佳，而河北安國和內蒙古產的則較差。The seed was also rich in total sugar, in crude protein, in amino acid and inorganic elements. in addition, the higher antimicrobial activity of alcohol extracts from the seed and pentadecanoic acid containing 18. 99 % in the unripe seed oils were first found
種子的總糖、粗蛋白、氨基酸、礦質元素含量也較豐富。首次發現種子醇提物有較強的抗菌活性和青果種子油有相對含量高達18 . 99的十五碳烷酸。Objective : construct high - level expression system of echistatin in e. coli methods : obtain amino - acid sequence of echistatin from genebank database. considering the bias of usage of 61 available aminoacid codons in e. coli, design the coding sequence of echistatin, synthesize the dna sequence chemically, get single copy coding gene and repeated two copy coding gene of echistatin. insert the sequence into expression vector pbv220, and more, we construct fusion expression clone of echistatin with pcr, identify the recombinant vector by dna sequencing
目的構建蛇毒鋸鱗蝰素（ echistatin ）的原核高效表達體系方法由genebank數據庫檢索蛇毒鋸鱗蝰素（ echistatin ）的氨基酸序列，結合大腸桿菌蛋白質合成體系對氨基酸密碼子使用的偏愛性，設計了echistatin編碼基因，體外人工合成編碼基因dna片段，通過適當的限制性內切酶位點插入表達載體pbv220 ，分別構建了echistatin的單拷貝表達克隆、雙拷貝串聯表達克隆；進一步通過pcr技術構建echistatin的融合表達基因克隆。A aada2 cassette, encoding aminoglycoside adenylyltransferase, was found in 2 isolates of shigella sonnei, and a two cassettes array of dfra1, encoding dihydrofolate reductase, and aadala in one isolate of shigella sonnei, and another two cassettes array of dfra1 7 and aada5 in two isolates of shigella sonnei and shigella flexneri y - variant each, and a dfrv cassette in one isolate of shigella flexneri 6, respectively
對其可變區測序分析，其中2株宋內志賀菌i類整合子均攜帶1個基因盒，為氨基糖昔腺營酞基轉移酶（ aminoglycosideadenylyltransferase ） az基因（ aa朔2 ） ，編碼對鏈黴素的抗性。Alpine orchard to apple for the quality of raw materials, the introduction of britain, germany, italy and other advanced production equipment and technology, the high - pressure cleaning, squeezing, enzymatic hydrolysis, instantaneous heat disinfection, ultrafiltration clarification, vacuum concentration, aseptic filling process from contain human needs of the various vitamins, amino acids and zinc, iron, copper and other trace elements, and maintain the natural juice taste, nutritional value high
產品簡介:以高山果園的優質蘋果為原料，引進英、德、意等先進生產設備和工藝，經高壓清洗、壓榨、酶解、瞬時高溫殺菌、超濾澄清、真空濃縮、無菌灌裝加工而成，蘊含人體需要的各種維生素、氨基酸及鋅、鐵、銅等微量元素，保持了果汁的天然口味，營養價值極高。In vitro antibacterial activity of a new aminoglycoside antibiotic, vertimicin
新氨基糖苷類抗生素威替米星的體外抗菌活性研究Abstract : from the angle of the functional requirement for underwear and outwear, this paper analyses the properties of anti - microbial and occlusion fabric produced from copper and polar amino acid of silks complex emetic reaction to distributed by cu s crystal on the surface of silk. it made a study on the producing method of elastic fabric and indicates the common problems in both production and design
文摘:從內衣對真絲的功能性要求及外衣對真絲綢成形能力的要求切入，介紹了利用銅化合物與桑蠶絲中的極性氨基酸發生絡合反應，在纖維表面形成硫化銅晶體得到抗菌導電真絲的原理和效果，還介紹了生產彈性真絲織物的幾種方法和影響織物彈性、服用效果的因素，提出了在生產、設計彈性真絲織物過程中應注意的主要問題。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。Secondly, we compared the amino acid sequences of ses and constructed the three - dimension structure of sed by homology modeling method. on the basis of results of comparing the amino acid sequences and structure of sed iv with other ses, we chosen the n23, f45, l59, n61, 192 and f203 in sed as mutant residues
對金葡菌超抗原家族的氨基酸序列進行對比分析，首次運用同源建模的方法構建了sed的三維空間結構模型，比較sed與其它腸毒素超抗原結構的差異，對可能的活性位點進行預測，最終確定sed的n23 、 f45 、 l59 、 n6 、 192和f203位氨基酸為突變位點。These results revealed that halocin c8 is cytocidal and its primary target might be located in the cell wall of the sensitive cells. two degenerate oligoxynucleotide primers ( c8 - 2, c8 - 4 ) were designed according to the n - terminal amino acid sequence of halocin c8
根據嗜鹽菌素cs的n端氨基酸序列設計了一對簡並引物（ cs一2 ， cs礴） ，利用這對引物從as7002的總dna中擴增出halcs的部分序列。To date there is no specific database for toxin and anti - nutrient proteins. in order to establish such a database, we have collected data from some nucleotide and protein database available at present. totally, 1033 toxin proteins, including 172 from plants, 251 from animals, 577 from bacteria and 42 from " other organisms, as well as 1013 lectins and 391 proteinase inhibitors are collected
本文通過對主要基因或蛋白數據庫進行檢索，收集散落於不同基因或蛋白數據庫中的毒蛋白氨基酸序列數據1033個，其中植物毒蛋白172個，動物毒蛋白251個，細菌毒蛋白557個，其它生物如真菌、藻類等的毒蛋白42個；抗營養因子蛋白數據1404個，其中凝集素1013個，蛋白酶抑制劑391個。Fr - 008 and streptomyces griseus imru3570 are two independently isolated producers for a similar heptaene macrolide antibiotic. comparative studies between the two producers at chemical and biological level are the main task of the present work, no obvious difference was observed on the hplc profiles
本文主要從化學和生物學兩個角度分析和比較了這兩個菌株的異同，並對抗生素的氨基海藻糖殘基基因進行了克隆嘗試。分享友人