陽菌 的英文怎麼說

中文拼音 [yángjūn]
陽菌 英文
prolapseofuterus
  • 陽 : Ⅰ名詞1 （太陽; 日光） the sun 2 （山的南面; 水的北面） south of a hill or north of a river 3 （中...
  • 菌 : 菌名詞1. （蕈） mushroom2. （姓氏） a surname
  1. The results showed that the main microbes in the koji used in naturally fermented liuyang brown bean were mainly molds and bacteria, and less counting of yeast and actinomyces

    結果表明：瀏陽豆豉自然制曲成熟的曲料中主要微生物為?菌類和細菌類，而酵母菌類和放線菌類數量不大。
  2. Cefotaximes has an especially favorable balance of activity againstgram - positive cocci, gram - negative aerobes, and someanaerobic organisms

    在抵抗革蘭氏陽性球菌、革蘭氏陰性需氧菌和部分厭氧菌中，頭孢他啶具有特別良好的作用。
  3. 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。
  4. The respiratory intensity of the contaminated soil decreased by 29. 93 % while ammonification and nitrification increased significantly than that of control soil. 2. extraction and purification of soil microbial total dna a method of extracting soil total dna was developed, and it can extract dna from g + bacteria

    二、土壤微生物總dna的提取和純化方法研究為了採用不依賴于培養的16srdna分析的方法研究有機磷農藥長期污染對土壤微生物群落結構的影響，建立了從土壤中提取總dna的方法，並通過改進使適合於對革蘭氏陽性菌的提取。
  5. An epidemiological analysis of bacillary in anyang city

    安陽市細菌性痢疾的流行病學分析
  6. We pay attention to the technical content of the product, carries on the deep processing to the product, introduces the bacteriolysis enzyme extraction technology of american group company, take the duck ' s egg as the raw material, extract the bacteriolysis enzyme that is widely applied to the medicine, the cosmetics, food anticorrosion and the bio - engineering fields of research, and we may extract 2500 kilograms every year ; we study the technology of maintaining egg product freshness with the shenyang agricultural college ; abandons with the national environmental protection agriculture using the project center, the dalian environmental science design research institute, the chwangho city environmental protection bureau jointly carries on the birds and beasts feed increase ecology conditioner expansion tests, makes zhuanghe city heidao agriculture comprehensive exploitation co., ltd the provincial level science and technology innovation enterprise

    莊河市黑島農業綜合開發有限公司在產品開發中注重提高產品的科技含量，對產品進行深加工，引進美國艾蒂集團公司溶菌酶提取技術，以鴨蛋為原料，提取廣泛應用於醫學、化妝品、食品防腐及生物工程研究領域的溶菌酶，年可提取2500公斤；與沈陽農業大學聯合研究蛋品保鮮技術；與國家環保農廢利用工程中心、大連市環境科學設計研究院、莊河市環保局聯合進行禽飼料添加生態調節劑擴大實驗，使黑島農業綜合開發有限公司成為省級科技創新型企業。
  7. Synthetic tendly oregano oil （ carvacrol ） oil of oregano has the properties of anti - bacterial ( gram - positive bacteria and gram negative bacteria ), anti - coccidia and anti - oxidant activity

    添德力牛至油（香芹酚）的生物活性幾乎對所有重要的革蘭氏陽性和革蘭氏陰性菌都有活性，同時還有抗真菌、抗球蟲和抗氧化特性。
  8. On cure, bacterium of positive of orchid family name is opposite most change penicillin is sensitive ; and bacterium of negative of change orchid family name is not sensitive to penicillin, and wait to streptomycin, chloromycetin sensitive

    在治療上，大多數革蘭氏陽性菌都對青霉素敏感；而革蘭氏陰性菌則對青霉素不敏感，而對鏈黴素、氯黴素等敏感。
  9. Bacterium of positive of orchid family name has common remove from office : bacili of grape coccus, streptococcic, pneumonic diplococcus, anthrax, diphtheria bacili, tetanic bacili ; bacterium of negative of orchid family name has common remove from office dysenteric bacili, typhoid bacillus, coliform organisms, be out of shape bacillus, green pus bacili, whooping cough bacili, choleraic vibrio reachs meningitis diplococcus to wait

    常見的革蘭氏陽性菌有：葡萄球菌、鏈球菌、肺炎雙球菌、炭疽桿菌、白喉桿菌、破傷風桿菌等；常見的革蘭氏陰性菌有痢疾桿菌、傷寒桿菌、大腸桿菌、變形桿菌、綠膿桿菌、百日咳桿菌、霍亂弧菌及腦膜炎雙球菌等。
  10. In this study, iltv - nm98a strain and iltv - wanggang strain were multiplied in chorioallantois. a pair of primers were devised according to the nucleic acid sequence of iltv tk gene and the dna of multiplied virus was used as pattern to amplify the gene of tk by polymerase chain reaction ( pcr ). the product of pcr was linked with suitable plasmid. then, the recombined plasmid was converted to escherichia coli. the converted escherichia coli

    根據已發表的iltvtk基因的核苷酸序列設計一對pcr引物，以增殖的兩株iltv的dna為模板，分別對它們的tk基因進行pcr擴增。將回收的pcr產物連接到適當的質粒載體上，轉化感受態大腸桿菌，通過篩選對iltvtk基因的陽性克隆進行擴增培養。
  11. Blood culture subsequently returned positive for clostridium septicum

    隨后的血培養敗血梭狀芽孢桿菌陽性。
  12. Milk and milk - based products - detection of thermonuclease produced by coagulase - positive staphylococci

    乳和以乳為基料的製品.凝固酶-陽性葡萄球菌的耐熱核酸酶檢測
  13. Microbiological examination of meat and meat products ; determination of coagulase - positive staphylococci ; by the drop method

    肉和肉製品微生物檢驗.凝結陽性葡萄球菌檢定.滴板法
  14. This tissue gram stain of an acute pneumonia demonstrates gram positive cocci that have been eaten by the numerous pmn ' s exuded into the alveolar space

    圖示：革蘭氏染色顯示大量滲出到肺泡腔的嗜中性粒細胞吞噬了革蘭陽性菌。
  15. 3 ) a heterotrophic nitrifier, named strain hn, was isolated from the greenhouse soil. the cells of isolates were gram positive, rod or coccus

    一3 ）從土壤中分離到一株異養型硝化細菌，命名為菌株hn ，分離菌株為革蘭氏染色陽性，球狀或桿狀。
  16. Law of coloring of change orchid family name, can be bacterial cent two kinds big : use method of this kind of coloring, it is to use gentian to catch a bug first, all bacteria caught purple, besmear again next with iodic fluid, will strengthen the tie of dye and bacterium body, the alcohol of 95 comes to reoccupy decolour 20 30 seconds, some bacteria not by decolour, still withhold purple, some bacteria are become by decolour colorless, reoccupy answer is red finally answer catch 1 minute, the result already was caught by the bacterium of decolour cheng gong is lubricious, not the bacterium of decolour still keeps purple, no longer chromatic, such, every is caught purple bacterium calls bacterium of positive of change orchid family name ; ran chenggong calls bacterium of negative of change orchid family name lubriciously

    革蘭氏染色法，能夠把細菌分為兩大類：採用這種染色方法，是先用龍膽紫來染病菌，所有細菌都染成了紫色，然後再塗以碘液，來加強染料與菌體的結合，再用95的酒精來脫色20 30秒鐘，有些細菌不被脫色，仍保留紫色，有些細菌被脫色變成無色，最後再用復紅復染1分鐘，結果已被脫色的細菌被染成紅色，未脫色的細菌仍然保持紫色，不再著色，這樣，凡被染成紫色的細菌稱為革蘭氏陽性菌；染成紅色的稱為革蘭氏陰性菌。
  17. A double - strand cdna fragment of dh ( diapause hormone ) gene was obtained from kt - pcr amplification. the fragment was digested by two restriction enzyme nde 1 / ecor 1 and then was joined with pet - 30a ( + ) plasmid which was digested by nde 1 / ecor 1 too. then the outcome was transformed into escherichia coli bl21

    Pcr產物經nde / ecor雙酶切后，與同樣雙酶切的pet - 30a （ + ）質粒連接並轉化至大腸桿菌（ escherichiacoli ） bl21中，經檢測篩選，成功得到陽性克隆。
  18. Construction and expression of yeast engineering yaccine : s14 / gnsag " as transformed to yeast host straln x33 by means of electroporation after ppiczaa s, . aresag " as l ined by saci enzyme. the single fungus, as choose and dibble inocu1ating in we and am plate, the positive fungus was gro ' ing in rm but not in w, and was 6 inoculated in ypd which included zeocine 500ug / ml and 1000ug / ml. 5 transformers were ampl if ied by pcr, three is same with positive control

    選取單個菌落分別點種到刪平板和md平板，找出在回d上生長正常， w上生長緩慢或不生長的菌落，即陽性菌落，再以陽性菌落分別塗布zeocine含量500ug加， 1000ug砌l的ypd平板，以高濃度的抗生素篩選高拷貝的酵母工程菌，在含500ug ml高濃度抗生素平板上獲得了15個轉化子，取其中5個進行pcr擴增，有3個擴增產物與陽性對照相同，說明此酵母細胞中已含有s hbsag融合片段，其中之一命名為p
  19. Distinguish above all so bacterium of cause of disease is bacterium of positive of change orchid family name or electronegative bacterium, choosing antibiotic respect meaning great

    所以首先區分病原菌是革蘭氏陽性菌還是陰性菌，在選擇抗生素方面意義重大。
  20. And the two pah ' s of pcr primers that bind to the adapter and the sequence of f fragment close by tn5 respectively were also designed. the genomic dna of b8 was isolated, digested with bamh i, and ligated to the adapter. using the two pairs of the primers, two rounds of pcr were performed hi turn and a fragment of 239bp was amplified successfully. lt was proved by cloning and sequencing that 18bp of the fragment is the sequence opposite to f fragment on the left of tn5 insertion site in b8f, the other is part of the 728 bp of f fragment. this result makes it possible to continue to carry out chromosome walking, to clone and sequence the whole genes of b fragment and f fragment, and to reveal the antagonistic molecular mechanism of b8

    試驗研究設計併合成了由40和44個堿基的寡聚脫氧核苷酸組成的染色體爬行接頭，在接頭序列和測定的f片段近tn5的序列上，設計了2對染色體爬行用的pcr引物，從b8菌株中提取基因組dna ， bamhi酶切，與染色體爬行接頭連接，依次用2對引物進行pcr ，擴增出239bp產物，經克隆、測序，發現其中18bp為擴增的相應于f片段在b8f菌株tn5插入位點對面的序列，其餘則為f片段728bp序列的一部分，為進一步進行染色體爬行，克隆和測定整個b和f基因，揭示陽菌株的拮抗分子機制提供了技術資料貯備。
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