短桿菌 的英文怎麼說

中文拼音 [duǎngǎnjūn]
短桿菌 英文
brevibacterium
  • 短 : Ⅰ形容詞（空間、時間兩端之間的距離小） short; brief Ⅱ動詞（缺少; 欠） lack; owe Ⅲ名詞1 （缺點） we...
  • 桿 : 桿名詞（桿子） pole; staff
  • 菌 : 菌名詞1. （蕈） mushroom2. （姓氏） a surname
  • 桿菌 : [微生物學] bacillus
  1. The subject of their research was gramicidin s, an antibiotic which had been isolated in the soviet union.

    她們研究的科目是短桿菌肽S，這是一種抗菌素。當時，蘇聯已經成功地離析了這種抗菌素。
  2. The subject of their research was gramicidin s, an antibiotic which had been isolated in the soviet union

    她們研究的科目是短桿菌肽s ，這是一種抗菌素。當時，蘇聯已經成功地離析了這種抗菌素。
  3. Conclusions : prokaryotic and eukaryocytic expression plasmids of the shortened hepatitis b surface antigen were successfully constracted, and the target proteins expressed by iptg induced in escherichia coli. as well as in eukaryocyte ( hepg2 and cos - 7 ), then their antigenity were detected

    結論：截短的乙型肝炎表面抗原分子的原核和真核表達』重組質粒成功被構建及分別在人腸桿菌efl得到誘導表達和存貞核細胞ifj表達，並檢測劍其表達產物的抗原特性。
  4. In order to provide theoritical foundation for the utilization of jerusalem artichoke ( ja ) resource, culturation of bifidobacteria and development of bifidobacteria products. this paper rather systernly studied the effects of ja on the growth of bifidobacteria, using jerusalem artichoke juice ( jaj ) and jerusalem artichoke powder ( jap ) as experimental material. in the first place, the effects of ja on the growth of bifidobacteria in vitro were studied. the results indicated that : jaj could stimulated the growth of b. longum ( blm ) and b. bifidwn ( bbm ) ; the more jaj content was added, the more promoting action was apparent ; the promoting action also varied from the different species. adding jap ( 3 % ) to skim milk could decrease the time of milk - solidfying of blm and bbm, and could increase the acid production in skim milk of the strains tested. secondly, bifidobacterium medium was developed using jaj as main material

    本文以菊芋汁和菊芋粉為主要材料，較系統地研究了菊芋對雙歧桿菌生長的影響，以期為進一步開發利用菊芋資源、雙歧桿菌的培養及其製品開發提供理論依據。菊芋在體外對雙歧桿菌生長的影響試驗表明，菊芋汁在體外對長雙歧桿菌（ blm ）和兩歧雙歧桿菌（ bbm ）的生長具有促進作用，其效果隨著菊芋汁添加量的增加而增加，並且對不同菌種的促生長效果存在差異；在脫脂乳中添加3的菊芋粉可以縮短blm和bbm的凝乳時間，其原因可能為促進了試驗雙歧桿菌在脫脂乳中的產酸。
  5. Full - length or truncated cdna was subcloned into prokaryotic expression vector pet30a and expression induced in e. coli bl21 ( de3 ). no squalene synthase polypeptide of expected molecular mass was observed in e. coli containing the putative full - length squalene synthase cdna, however, overexpression in e. coli was achieved by truncating 30 hydrophobic amino acids at the carboxy terminus

    但在含有全長的鯊烯合酶cdna的大腸桿菌中並沒有觀察到預期大小的鯊烯合酶表達，而c末端截短30個疏水氨基酸的鯊烯合酶可在大腸桿菌中過量表達。
  6. 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

    將來自短小芽抱桿菌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 ）插入到大腸桿菌-枯草桿菌穿梭質粒載體psugv4中，構建成表達質粒psu一bpap 。
  7. Conclusion a systematic method for preparation of enzyme - mannanse is established, a high productive strain was got after seducing and selecting from nature, confirmed as brachybacterium spa6 research were conducted on medium and culture method of the strain in order to get the suitable cultural condition of fermentation, the experiment result shows the optimium condition is ph7. 0, temperature 36c ; carbon content 2. 5 %, ventilation in abundence, agitation speed 200r / min

    結論1 、以從自然界中篩選出的菌株為出發株，經誘變、篩選，得一高產葡甘聚糖酶菌株，初步鑒定為短桿菌屬brachybacteriumspa6 2 、經誘變、三角瓶培養，該菌株的最適培養條件：培養基ph值7 . 0 ，碳源2 . 5 ，振蕩培養， 200r min ，培養溫度36 ，培養48h 。
  8. Was supplied. its essential characteristics are as follows : short rods, 2. 0x1. 6 ^ m in diameter, arranged singly, gram negative, facultatively anaerobic, having both a respiratory and a fermentative type of metabolism, oxidase negative and catalase positive

    通過形態觀察及生理生化特徵測定發現菌株w12為革蘭氏陰性菌，短桿狀，對數生長期細胞大小為： 2 . 0 1 . 6 m ，單個排列；兼性厭氧，氧化酶陰性，發酵葡萄糖產酸產氣，不運動。
  9. In this article, the author amplified dna sequences encoding the mature peptides of human intact and truncated igf - 1 gene from human genomic dna by the new way of alternative pcr established and named as exons - piecing together method by this laboratory. the igf - 1 and des ( l - 3 ) igf - l gene were cloned in pgem - t vector and then subcloned in expression plasmid pgex - 3x. two recombinant constructs known as pgex - 3x - igf - l and pgex - 3x - des ( l - 3 ) igf - l were transformed to e. coli dh5 a respectively

    我們利用外顯子拼接法從人的基因組dna中擴增了編碼完整型及截短型人igf - 1基因成熟肽的dna片段，並將其克隆至pgem - t載體中；經測序證明正確后，又構建了表達載體pgex - 3x - igf - 1及pgex - 3x - des （ 1 - 3 ） igf - 1 ，在大腸桿菌中進行了表達研究。
  10. Bacillus pumilus un - 31 - c - 42 was obtained by mutations of strain ba ( 06 ), which is an alkaline protease producer and separated from life waste in chengdu

    短小芽孢桿菌（ bacilluspumilus ） un - 42 - c - 31是一株從成都市生活垃圾中分離，經過多次反復誘變后得到的堿性蛋白酶產生菌。
  11. The result of sequencing shows that this fragment contains an open reading frame of 1106 nucleotides and encodes 369 amino acids residues, which is part of a alkaline serine protease, with 98. 3 % homogeneity to a reported gene from bacillus pumilus

    序列分析顯示，該片段是一個全長1106bp的orf ，可編碼369個氨基酸殘基的多肽，與短小芽孢桿菌堿性蛋白酶基因編碼區高度同源。
  12. A pair of primers, based on the high homologous n - and c - terminal amino acids sequences of subtilisin of bacillus pumilus, were designed and used to amplify subtilisin gene from genomic dna of 4 different bacillus strains by polymerase chain reaction

    Sds 、 edta和pmsf對酶活力有不同程度的抑制作用。以4株芽孢桿菌的總dna為模版，利用擴增短小芽孢桿菌堿性蛋白酶基因的引物對它們進行pcr擴增。
  13. The enzyme activity in fermentation liquid could be inhibited by pmsf and dfp. the fermentation liquor also showed good dehairing activity. the alkaline protease ( named dhap, dehairing alkaline protease ) in the fermentation liquid was purified with hydrophobic interaction chromatography, ion exchange and gel filtration

    通過cm - sepharosefastflow離子交換層析， deae - sepharosefastflow離子交換層析， sephacryls - 100 ， sephacryls - 200凝膠過濾層析，疏水層析等純化步驟對短小芽孢桿菌發酵液中的堿性蛋白酶進行了純化。
  14. High performance ion exchange chromatography was applied in studying qualitatively and quantitatively of bacteria, which was shown as follows : firstly, physio - biochemical characteristics of bacteria was investigated by ion exchange chromatography. for the first time spores and nutrient of bacillus pumilus had been separated successfully by chromatography. chromatographial behaviors of bacteria at different cultivating environment and different growth phase were also studied

    本文利用高效液相離子交換色譜系統研究細菌學，探討了該方法在細菌定性、定量方面的應用，主要包括三個方面：首先，利用離子交換色譜系統表徵細菌生理、生態方面的變化，首次成功地在色譜上區分了短小芽孢桿菌的芽孢及營養體；考察了不同的培養環境對細菌色譜行為的影響及不同生長階段的細菌的色譜行為。
  15. Objective : to construct prokaryotic and eukaryocytic expression plasmids of the shortened hepatitis b surface antigen, and express the target proteins by iptg induced in escherichia coli

    目的：構建截短的乙型肝炎表面抗原分子的原核和真核表達重組質粒，然後分別在大腸桿菌中誘導表達並純化表達蛋白及在真核細胞中表達目的基因，並檢測其抗原特性。
  16. 5 lahaie rg, a randomized trial of the efficacy of three regimens for t he eradication of helicobacter pylori. gastroenterology 1995 ; 108 : a141

    6劉文忠，呂寶妹，蕭樹東等.含克拉黴素的短程三聯療法根除幽門螺桿菌.中華內科雜志1996 ； 35 ： 803 - 806
  17. Bacteria was further improved in 1997 when a chromogenic medium clecc was introduced, and reporting time was shortened from three to just one and a half days. photo of appearance of

    這套分析方法一直沿用至今，但培養大腸桿菌的介質媒體則在1997年進一步改良，採用可發色體培養基clecc ，報告時間亦由3天縮短至1 . 5天。
  18. Abstract : techniques of apple genetic transformation can improve apple trees and shorten the breeding cycle by molecular methods. in the last years, great progress has been made in this field, which involves a number of important apple genotypes developed. so far, apple genetic ransformation mainly adopts agrobacterium - mediated technique, involving infection and transgenic tissue regeneration, which are important steps to affect the transformation efficiency. the initial work to the date is to know and to search for the factors which can increase the efficiency

    摘要蘋果的遺傳轉化技術通過分子手段改良蘋果，有助於縮短其育種周期.最近十年，在該領域的研究取得很大進展，涉及到一些重要的蘋果基因型及有用的外源基因.迄今，蘋果的遺傳轉化主要採用農桿菌介導法，侵染與轉化材料的再生是影響其轉化效率的關鍵過程，了解其影響因素，尋找有利因素以提高轉化效率是目前蘋果遺傳轉化研究的重點。
  19. The homologous analysis showed that the n - terminal sequence of dhap is identical to that of serine protease from another b. pumilus strain tyo - 67 and has high homology with those from other bacillus species. based on the homologous analysis, three pairs of primers were designed and synthesized

    該序列與來自其它芽抱桿菌屬菌株的絲氨酸蛋白酶的n一末端氨基酸序列有較高的同源性，並和另一株短小芽抱桿菌的絲氨酸蛋白酶n一末端氨基酸序列完全一致。
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