枯草桿菌 的英文怎麼說

中文拼音 [cǎogǎnjūn]
枯草桿菌 英文
bacillus subilis
  • : 形容詞1 (植物等失去水分; 乾枯) (of a plant etc ) withered 2 (井、河流等變得沒有水) (of a w...
  • : Ⅰ名詞1 (草本植物的統稱) grass 2 (指用作燃料、飼料等的稻、麥之類的莖和葉) straw 3 (草稿) dra...
  • : 桿名詞(桿子) pole; staff
  • : 菌名詞1. (蕈) mushroom2. (姓氏) a surname
  • 桿菌 : [微生物學] bacillus
  1. Apply a small amount of bacitracin to your nipple immediately after breaking the blister

    小泡破了以後立刻在乳頭上塗少量的枯草桿菌抗生素( ? ) 。
  2. Used as 1. 1094 strain of bacillus subtilis as researched material, the structural genes of biotin operon ( bio operon ) were cloned, and its sequence were engineered

    本研究以枯草桿菌asl . 1094株為研究材料,克隆了生物素操縱子基因,並對基因序列進行改造。
  3. Used the genomic dna extracted by low melting - point agarose embedding method as pcr template, the full length of structural genes of bacillus subtilis bio operon were gained by long pcr method

    將該方法提取的基因組dna稀釋100倍作為模板,採用長距離pcr方法,獲得了枯草桿菌生物素操縱子基因全長。
  4. Promoting action of pilose autler for b. subtilis

    鹿茸對枯草桿菌的促作用
  5. In order to express alkaline protease gene ( ap gene ) in bacillus subtil is, the recombinant expression plasmid was constructed. this plasmid contains a promoter bp53, also from b. pumilus un - 31 - c - 42, ap gene and the shuttle vector psugv4. after introduced into b. subtilis wb600, the transformants displayed the hydrolyzed zone on milk plate

    將來自短小芽抱un一31一c礴2的基因啟動子( bp53片段)和脫毛蛋白酶全基因( ap )進行融合,然後將重組基因(命名為bpap )插入到大腸-枯草桿菌穿梭質粒載體psugv4中,構建成表達質粒psu一bpap 。
  6. The substance with antibacteria action which had high purity was tested with escherichia coli, staphylococcus aureus, bacillus pyocyaneus and yeast by the antibacteria test to decide the minimal inhibitory concentration as 6. 37umol. l - 1, 3. 18umol. l - 1, 6. 37umol. l - 1, 6. 37umol. l - 1 25. 48umol. l - 1

    純化的抗活性物質通過對大腸、金黃色葡萄球枯草桿菌、綠膿、酵母做抑試驗,最低抑濃度分別為6 . 37 mol
  7. Based on the a - amylase - catalyzed hydrolysis of starch, pqci method has been developed to monitor the growth process of bacillus subtilis and the variation of the a - amylase activity during the growth. bacteria growth equations were derived based on the kinetics of the enzyme - catalyzed hydrolysis of starch

    將pqci技術應用於對枯草桿菌生長的研究,並且基於-澱粉酶對水溶性澱粉的酶促反應,推導出了枯草桿菌的pqci生長模型,包括諧振頻率、動態電阻和動態電感模型。
  8. Besides, vgb gene expression also increased the chitinase secretion. in order to make the vitreoscilla hemoglobin gene express in bacillus subtilis, an inducible promoter ( levansucrase ) was cloned from b. subtilis wb600 and ligated with a promoter - less vgb gene. the resulted gene is called sacvgb and was demonstrated to express in e, coli by sds - page and carbon monoxide binding assay

    由於vgb基因啟動子不能在枯草桿菌中啟動表達,因此,根據已發表的果聚糖蔗糖酶基因( sacb )序列設計引物,從枯草桿菌wb600總dna中擴增出該基因的啟動子片段,然後將其與vgb基因編碼區及終止子序列相連,成功地組建了sacvgb融合基因。
  9. The results also explained that it was feasible that the genomic dna of bacillus subtilis were extracted and gained large dna fragments by low melting - point agarose embedding method

    說明以低熔點瓊脂糖包埋法提取枯草桿菌基因組dna ,並獲得較大的dna片段,是完全可行的。
  10. Extraction of large - fragment genomic dna in order to gain dna template of pcr amplification ( long pcr amplification and salvage pcr amplification ) which was high purity and large fragment, three methods were used to extract genomic dna of bacillus subtilis, i. e. low melting - point agarose embedding method, sds - proteinase k - phenol chloroform extraction method and bacterial genomic dna extraction kit method. the genomic dna of bacillus subtilis were gained by these methods, and the operated programs of the methods were improved. the results showed that the genomic dna extracted by low melting - point agarose embedding method were obviously biggest than that of another two methods

    大片段基因組dna的提取為了獲得用於pcr擴增(長距離pcr擴增和分段pcr擴增)的高純度、大片段(至少為pcr產物長度的4倍)的dna模板,應用三種方法:低熔點瓊脂糖包埋法, sds -蛋白酶k -酚氯仿抽提法和細基因組dna提取試劑盒法,分別提取獲得了枯草桿菌基因組dna ,並對3種方法的操作程序進行了不同程度的改進,結果表明:低熔點瓊脂糖包埋法提取的基因組dna片段明顯大於后兩種方法,採用0 . 5瓊脂糖凝膠電泳3h ,仍然跑不出加樣孔。
  11. Contrasting analysis with the genes sequence of bacillus subtilis 168 strain ' s bio operon, the sequence of bio operon of as 1. 1094 strain had 12 bases difference with that of 168 train, and 7 bases caused variation of amino acid

    1094株與168株bioafdb基因序列完全一致, 9個差異堿基是由於pcr擴增導致的。枯草桿菌生物素操縱子基因4個亞克隆序列的測序結果證實, asi
  12. 2. cloning of structural genes of bacillus subtilis bio operon diluted the genomic dna of bacillus subtilis as the template, long pcr product ( 10. 3kb ) and three salvage pcr products were separately gained by optimization of reaction conditions of pcr

    枯草桿菌生物素操縱子基因的克隆將枯草桿菌基因組dna稀釋后,通過pcr反應條件的優化,分別擴增得到了生物素操縱子基因的長距離pcr產物( 10 . 3kb )和3個分段pcr產物。
  13. Progress in research of the fibrinolytic enzyme in fermented soy sauce

    海參液態發酵制備枯草桿菌蛋白酶的研究
  14. Optimization of fermentation process on a fibrinolytic enzyme from bacillus subtilis sbs

    枯草桿菌溶栓酶的分離純化研究
  15. In fact, b. subtilis is fairly robust in terms of its radiation resistance

    事實上,就輻射防禦而言,枯草桿菌算是相當耐命。
  16. Kinetic parameter estimation of do - stat batch fermentation of thrombolytic enzyme by bacillus subtilis hl

    枯草桿菌溶栓酶恆溶氧發酵動力學參數估計
  17. The sequence around these residues revealed that ap was a new member of the subtilisin family

    該蛋白酶可以認為是枯草桿菌蛋白酶家族( subtilisin )的新成員。
  18. Study on the optimization of fermentation conditions of a strain fibrinolytic enzyme producing bacillus subtilis

    1株誘變的枯草桿菌溶栓酶體內外溶栓性質初探
  19. The expression plasmid called psugv - badfe was constructed by inserting ba - dfe gene into e. coli - b. subtilis shuttle vector psugv4 and the

    將ba0fe基因克隆到大腸枯草桿菌穿梭載體psugv4中,得到重組質粒psugv badfe ,然後轉化到枯草桿菌wb600中進行了分泌表達。
  20. B. amyloliquefaciens dc - 4 was firstly found to produce a fibinolytic enzyme. the optimal fermentation conditions for producing ba - dfe were determined and the results are as follows

    它們產生的溶栓酶分別命名為枯草桿菌豆豉溶栓酶( bs - dfe )和解澱粉芽孢豆豉溶栓酶( ba - dfe ) 。
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