細菌鑒定 的英文怎麼說

中文拼音 [xìjūnjiàndìng]
細菌鑒定 英文
identification of bacteria
  • 細 : 形容詞1 （條狀物橫剖面小） thin; slender 2 （顆粒小） in small particles; fine 3 （音量小） thin ...
  • 菌 : 菌名詞1. （蕈） mushroom2. （姓氏） a surname
  • 鑒 : Ⅰ名詞1 （鏡子 古代用銅製成） ancient bronze mirror2 （可以作為警戒或引為教訓的事） warning; objec...
  • 定 : Ⅰ形容詞1 （平靜; 穩定） calm; stable 2 （已經確定的; 不改變的） fixed; settled; established Ⅱ動詞...
  • 細菌 : germ; bacterium （pl. bacteria）; fungus （pl. fungi）
  • 鑒定 : 1 （評語） appraisal （of a person s strong and weak points） 2 （評定） appraise; identify; auth...
  1. Newcastle disease virus ( ndv ) strain 695, a thermostable nature avirulent strain, were replicated in embryonated chicken eggsand its rna was extracted from allantoic fluid. referred to the reported sequence of f gene, a pair of primers were designed and synthesized. f gene of ndv b95 strain was amplified by rt - pcr, the pcr products were checked by agrose gel electrophoresis and purified by agrose gel fracion method

    利用從國外引進的新城疫熱穩定性天然弱毒b _ （ 95 ）株接種spf雞胚繁殖病毒，經處理后提取病毒的基因組rna ，參考國內外發表的ndv融合蛋白基因序列，設計一對特異性引物，經反轉錄聚合酶鏈式反應（ rt - pcr ）擴增出約1700bp大小的特異性片段，將此片段回收純化后，利用t - a克隆技術將其克隆到pgem - t - easy克隆載體中，再轉化大腸桿菌jm109感受態細胞，轉化后經分子量比較、 pcr鑒定和酶切分析篩選陽性克隆。
  2. The properties of morphology and physiology of this strain was studied. according to bergey ' s manual of determinative bacteriology, the strain was identified as a new strain of the sporocytophaga

    通過對其形態及其生理生化特性的研究，該菌株被鑒定為生孢噬纖維細菌屬（ sporocytophaga ）的一個新菌株。
  3. Isolation and identification of bacteria in burley curing process

    白肋煙晾制期間煙葉中細菌的分離和鑒定
  4. Studies on isolation, identification and characteristics of reducing tsna contents of burley tobacco endophytic bacteria

    一株降低煙草中特有亞硝胺細菌的分離鑒定及特性研究
  5. Separation and lytic study of one algae - lysing bacteria

    一株溶藻細菌的分離鑒定及其溶藻效應初探
  6. Serious cross reation existed between v. albo - atrum and mv2, mv3, mv4. the other pathogen isolates v31 and v32 also had cross reactions, but the reaction was not serious. because limited number of pathogen isolates were selected, it could not prove that the selected immunogen was widely presentative, more pathogens isolates should be tested to verify the acquired hybridomas cells

    5株單抗雜交瘤細胞中沒有一株具有種或屬的特異性，其中mv2在棉花黃萎病菌若干菌系間的檢測表明其能夠區分不同的致病類型； mv1和mv4組合檢測的結果基本上能將棉花大麗輪枝菌鑒定到種；黑白輪枝菌與mv2 ， mv3 ， mv4的交叉反應比較強烈，其他菌株v3 ， v32有個別的交叉反應，但不強烈
  7. Among them, the strain a has the highest activity and the fucoidanase activity is as high as 3. 68u. after the thalli and colony features are analyzed, the strain a is identified to be erysipelothrix rosenbach according to bergey ' s manual of determinative bacteriology

    通過對該菌株a個體形態，菌落形態及生理生化特徵的分析，依據《伯傑氏細菌鑒定手冊》 ，暫確定其歸屬于丹毒絲菌屬（ erysipelothrixrosenbach ） 。
  8. After further purifing the isoloated bacteria, we classified and characterized them, according to their individual form, physiological and biochemical to characterize, characterize to bacteria genus. calculated the total of aerobic bacteria in soil of each senson, the total of bacteria of degrading omethoate, as well as the percentage of each degradation bacteria genus, and measured the physico chemical nature of each seasonal soil sample

    將分離到的菌株進一步純化后，按其個體形態、生理生化特徵，進行分類鑒定，鑒定到菌屬；計算出各季節土壤中的細菌總數、降解有機磷農藥氧樂果的細菌總數以及各降解菌屬的百分比，測出各季節土壤樣品的物理化學性質。
  9. Identification of functional bacteria showed predominant ammonifiers were shewanella, variovorax, chryseobacterium, bacillus or aeromonas ; among 4 selected nitrogen fixers, one ( azorhizobium caulinodans ) belonged to. a - proteobacteria, the other three ( serratia marcescens, klebsiella pneumoniae and citrobacter freundii ) were enterobacteriace, which belongs to - proteobacteria ; 2 nitrate reducers were aeromonas sp. and citrobacter sp.,

    對各功能菌群中的優勢菌的鑒定表明，優勢的氨化細菌為希瓦氏菌屬，產堿菌屬，黃桿菌屬，芽孢桿菌屬或氣單胞菌屬；分離到的4個優勢固氮細菌菌株中，一株為基瘤固氮根瘤菌，屬于-變形菌亞門，而另外3株都屬于腸桿菌科，歸于-變形菌亞門。
  10. Culture of mg7 hybridoma cells and detection of antigen - binding affinity of mg7 mab by elisa 2. construction and identification of mg7 recombinant phage antibody library mrna was isolated from cultured mg7 hybridoma cells and converted into cdna ; the variable fragments of heavy and light chain were separately amplified and assembled into scfvs with a specially constructed dna linker by pcr. the scfvs dma was ligated into the phagmid vector pcantabse and the ligated sample was transfered into competent e. co / / tg1 to generate a bacterial form of mg7recombinant phage antibody library ; volume and recombinant ratio of the library were evaluated by means of bacterial colony counts and restriction analysis ( ecor i and hind iii )

    Mg _ 7重組噬菌體抗體庫的構建及鑒定從培養的mg _ 7雜交瘤細胞中提取並分離mrna ，反轉錄成cdna ；利用pcr分別擴增mg _ 7單抗的重鏈及輕鏈可變區基因，並通過? dna連接子將二者連接起來形成mg _ 7單鏈抗體基因；將mg _ 7單鏈抗體基因插入pcantab5e ；將連接產物轉化感受態tg1大腸桿菌，制備細菌形式的mg _ 7重組噬菌體抗體庫；通過菌落計數和限制性酶切分析（ ecor和hind ）評估mg _ 7重組噬菌體抗體庫的容量和重組率。
  11. Hi and ni assays were performed to detect the subtype of viruses if ha test was positive ( ad 16 ) and contamination test was negative

    血凝陽性（ ad ） 16 ）且細菌培養陰性標本進一步做hi和ni實驗以鑒定亞型，標本保存於一80箱。
  12. Materials and methods : fecal, cloacal and tracheal swabs from different types of poultry were collected in 6 live - bird retail markets once a week. they were inoculated into 9 - 11 days embryonated chicken eggs and incubated in 35 " c for 72 hours. hi and nl assays were performed to detect the subtype of viruses if ha test were positive ( ad ^ 16 ) and contamination test were negative

    材料和方法：每星期收集一次標本，收集的標本常規處理， 9 - 11日齡雞胚尿囊腔接種， 35培養72小時，收取尿囊液，血凝陽性（ ad 16 ）且細菌培養陰性者- 70保存並進一步做hi ， ni實驗鑒定亞型。
  13. Methods of quarantine and identification of acidovorax avenae subsp. citrulli

    西瓜細菌性果斑病菌檢疫鑒定方法
  14. Selected 104 samples from cattle bacterial diarrhea cases in part of shaanxi province, the pathogen isolation and identification results showed that the main bacterial pathogen were pathogenic escherichia coli., salmonella, clostridium welchii, pasteurella pestis etc., the escherichia coli. predominant serotypes o groups were o2, o86, o138

    摘要採取陜西省部分地區細菌性犢牛腹瀉病料104份，進行病原細菌的分離鑒定，結果表明，引起該地區犢牛腹瀉的細菌性病原主要是致病性大腸桿菌、沙門氏菌、魏氏梭菌、多殺性巴氏桿菌等；大腸桿菌主要以o2 、 o86 、 o138為優勢血清型。
  15. Isolation and identification of bacteria from gastrointestinal tract of ceroplastes japonicus green

    日本龜蠟蚧腸道細菌分離及鑒定研究
  16. The results showed about 490bp dna fragments were amplified. because the amplified products is specific to the p - subclass of the proteobacteria, the amplification of the amoa gene may be a powerful molecular tools for detecting and analyzing ammonia - oxidizing communities in environment

    由於基於此引物的擴增對proteobacteria -亞科氨氧化細菌具有特異性，所以amoa基因片段的特異擴增為我們檢測和鑒定環境樣品中氨氧化細菌的種群提供了一個有效的工具。
  17. Benzyl chloride were used for extracting genomic dna of aspergillus. niger 14, about 1. 5kb specific fragment was obtained from genomic dna of aspergillus. niger 14 by pcr amplification with primers ( forward primer5 " ataggcatcatgggcgtctct3 " reverse - primer5 " cagctaagcaaaacactccgc 3 designed according to the known sequences of the phytase gene in the gene bank and pyrobest ? dna polymerase, after ligated with pmd18 - tvector, transformated into e. colidh5a competent cell successfully. 3. nucleotide sequence analysis of the cloned fragment revealed the presence of the whole phya gene in pcr product

    用氯化芐法提取了aspergillus . niger14 ~ #基因組dna ，根據genebank中已知的黑麴黴植酸酶基因序列設計出一對特異性引物（上游引物： 5 ataggcatcatgggcgtctc3下游引物： 5 cagctaagcaaaacactccgc3 ） ，採用pyrobest ~ （ tm ） dnapolymerase （高保真dna聚合酶） ，通過pcr方法從aspergillus . niger14 ~ #基因組dna中擴增出了預期的1 . 5kb左右的特異性產物，將其與pmd18 - tvector連接后，轉化e . colidh5菌株的感受態細胞，經質粒抽提、酶切鑒定，確認該目的產物已得到成功克隆。
  18. Identification area : the main equipment here is an ordinary micro - scope, on fluorescence microscope, incubator, instrument for bacte - ria identification, low temperature or ultra low temperature refrigera - tor ( for the temporary storage of bacteria shall follow the regulations of the cdc )

    3鑒定區：主要有普通顯微鏡、熒光顯微鏡、溫箱、細菌鑒定儀、低溫或超低溫冰箱（菌種臨時保存，視cdc規定而定）等。
  19. Among them an isolated bacterial strain secreting a large amount of alkaline lipases was selected. by testing morphologic and physiological - biochemical characteristics the strain was identified as pseudomonas sp.

    參考伯傑氏細菌鑒定手冊，經形態觀察和生理生化實驗，初步鑒定為假單胞菌（ pseudomonassp . lz1 ） 。
  20. Methods the bacterium determine that adopts api system and craft law, the quick test of medicine adopts k - b law, the result judge that carries out according to nccls standard

    方法細菌鑒定採用api系統和手工法，藥敏試驗採用k - b法，結果判定按nccls標準執行。
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