溶菌體 的英文怎麼說

中文拼音 [róngjūntǐ]
溶菌體 英文
lysosomes
  • 溶 : 動詞（溶化; 溶解） dissolve
  • 菌 : 菌名詞1. （蕈） mushroom2. （姓氏） a surname
  • 體 : 體構詞成分。
  1. The inclusion bodies of recombinant protein were purified with washing buffer consisting of various urea ( 2mol / l and 4mol / l ) for several times, and then dissolve the fusion protein in the denature buffer using 8mol / l urea as denaturant

    用含有2mol l和4mol l尿素的包涵體洗滌液洗滌包涵體，在37條件下，洗去了大部分菌體蛋白及其它核酸物質。用8mol l尿素作為變性劑溶解包涵體，包涵體在8mol l尿素中的溶解性非常好。
  2. As well as providing a new tool to combat bacteria now, there is interest in developing bacteriophage lysins to replace antibiotics in some applications in the future

    作為對抗這些細菌的新的藥物工具，人們對將來開發噬菌體細胞溶解酶在某些條件下代替抗生素產生了濃厚的興趣。
  3. The bacteria - bursting enzymes that caught gasson s attention are called lysins. different lysins attack specific bacteria and the bacteriophage lysins researched by gasson s team can be used to detect or selectively kill listeria and clostridium

    不同的細胞溶解酶攻擊特定的細胞，加森小組所研究的噬菌體細胞溶解酶可用於探測或選擇性地殺死李斯特氏菌和梭狀芽孢桿菌。
  4. Only prokaryotes, such as bacteria, lack lysosomes.

    只有細菌這樣的原核生物才沒有溶酶體。
  5. Lysogeny is a semi-permanent association between the phage and host chromosoes.

    溶源性是噬菌體和寄生染色體之間的半永久聯合
  6. Its content was about 9. 8 % among total cell protein by gene genius bio imaging system. the fusion proteins were found largely in an insoluble inclusion bodies. the purified fusion proteins was obtained by his6 technique used to immunize rabbits to obtain polyclonal antiserum with titer of 1 * 105

    經工ptg誘導，重組質粒在點co力『 blzi中表達出了c端融合了6xhis的融合蛋白，過量表達的蛋白主要以不溶性蛋白形式存在，其表達量占菌體總蛋白的9 . 8 % 。
  7. Abstract : the article introduces the application of cold sterilization, super high pressuer sterilization, sterilization system of hydrogen peroxide - peroxidase - glucose oxidase, uht, htst, radioactive sterilization and lysozyme sterilization to the production of tea beverage ， and predicts their future prospect

    文摘:介紹了冷滅菌、超高壓殺菌、過氧化氫-過氧化氫酶-葡萄糖氧化酶體系殺菌、超高溫殺菌、高溫瞬時殺菌、輻照殺菌和溶菌酶殺菌等技術在茶飲料生產上的應用，展望了其應用前景。
  8. The article introduces the application of cold sterilization, super high pressuer sterilization, sterilization system of hydrogen peroxide - peroxidase - glucose oxidase, uht, htst, radioactive sterilization and lysozyme sterilization to the production of tea beverage ， and predicts their future prospect

    介紹了冷滅菌、超高壓殺菌、過氧化氫-過氧化氫酶-葡萄糖氧化酶體系殺菌、超高溫殺菌、高溫瞬時殺菌、輻照殺菌和溶菌酶殺菌等技術在茶飲料生產上的應用，展望了其應用前景。
  9. The results of lauryl sodium sulfate - polyacrylamide gel electrophoreses ( sds - page ) of the aggregate precipitate and supernatant and the result of high - performance size - exclusion chromatography of the supernatant indicated that, by wrongly linked intermolecular disulfide bonds soluble bi - molecular and tri - molecular egg white lysozyme aggregate could be simultaneously formed except being renatured to native and active egg white lysozymes during the refolding procedure of denatured - reduced egg white lysozyme ; the aggregate precipitate could be further formed by the non - covalent bonds interaction between the soluble hi - molecular egg white lysozyme aggregates, and the soluble tri - molecular egg white lysozyme aggregate could still stay at the supernatant

    沉澱和上清液的不連續十二烷基硫酸鈉聚丙烯酰胺凝膠電泳（ sds - page ）和高效凝膠排阻層析分析結果表明，還原脲變性蛋白溶菌酶在稀釋復性過程中除了能夠復性成天然態蛋白溶菌酶分子外，還會形成可溶的蛋白溶菌酶分子二聚體和三聚體，二聚體和三聚體主要是靠分子間二硫鍵的錯配連接而成的；可溶的蛋白溶菌酶分子二聚體之間通過非共價鍵相互作用而形成集聚體沉澱，而可溶的三聚體溶菌酶分子則仍處于復性液上清液中。
  10. Result bl21 with pgex - 4t - l - nk4 could correctly the targeting protein. the bacteria were cultured for 2h before being induced by iptg. the high - level production was got by being induced at 37 for 2h

    結果發現:在37菌體以包涵體的形式表達，在朋菌體1 :要以可溶性狀態表達，在25 「 c菌體也以包涵體形式表達。
  11. First, after investigation of two original strains " biological characteristics, we studied the main influence factors on protoplasts formation and regeneration in s. mycarofaciens and s. erythreus, and determined the best protoplasts formation and regeneration conditions of two original strains. the former shake - cultured in s " medium at 28 ?, 220r. min ~ ( - 1 ) for 24h, lysised by 3mg / ml lysozyme, keeping warm at 32 ? for 50 ~ 60min, regenerated on r _ ( 5 " ) medium, 28 ? for 5 ~ 6d. the latter used two - step culture, then used img / ml lysozyme keeping warm at 37 ? for ih ; the protoplasts were plated on r5 " regeneration medium at 28 ? for 5d

    首先在對兩親株的生物學特性進行了鑒定后，考察了影響兩親株原生質體形成和再生的主要因素，確定了生米卡鏈黴菌和紅黴素鏈黴菌原生質體形成及再生的最佳條件：前者用s培養基，在28 、 220r . min ~ （ - 1 ）培養24h后，用3mg ml的溶菌酶在32恆溫酶解50 60min ，得到的原生質體在乾燥的r5培養基上28倒置培養5 6天，可得到再生率在20左右的再生菌落；後者採用二級菌絲培養，用1mg ml的溶菌酶在37恆溫酶解1h左右，得到的原生質體也在乾燥的r5培養基上28倒置培養5天，即可得到再生率在20左右的再生菌。
  12. This paper describes several latest industrial microbial technologies in detail, which are the synthesis of the chiral diols by epoxide hydrolase from microbie, cofactors regeneration for redox with fdh, production of nano / micro wire by the phage display, metabolic network rebuilding for conventional fermentation and the application of the organic solvent tolerance and the metagenomics technology

    本文綜述了幾項最新的工業微生物技術，主要包括：微生物環氧化水解酶催化合成手性二醇、微生物甲酸脫氫酶用於再生氧化還原反應的輔因子、通過噬菌體展示技術得到納米級金屬絲、代謝網路改造和重建用於傳統發酵生產以及有機溶劑耐受菌和宏基因組技術的應用。
  13. Understanding how the bacteria grow and avoid lysosomes might suggest new ways to forestall or halt the infection

    了解披衣菌如何生長及避開溶小體，將可能提供預防或阻擋感染的新方法。
  14. If the lysosomes cannot provide bits of the bacteria for display on the cell surface, patrolling t cells will not recognize that a cell harbors invaders

    溶小體未能將披衣菌碎片呈現在細胞表面，巡邏的t細胞便不曉得哪個細胞窩藏了入侵者。
  15. P hage induction following conjugation of a lysogenic bacterium with a nonlysogenic one

    伴隨著溶源菌與非溶源菌接合的噬菌體誘導。
  16. A novel aqueous two - phase system can be formed by the mixtures of a polymer and cationicanionic surfactants. such a system can be used as a partitioning system of proteins. in this work, we investigated the formation, phase behavior and protein partitioning in aqueous two - phase systems formed by dodecyltriethylammonium bromide / sodium dodecylsulfate / peg and dodecyltriethylammonium bromide / sodium dodecylsulfate / dextran. the ligands with affinity were attached to the polymers and the affinity partitioning of proteins was investigated. it was shown that the surfactants and polymers are enriched in different phases of aqueous two - phase systems. phase separation are promoted by increasing temperature and adding inorganic salts. different proteins are partitioned in different phases. the selectivity of protein partitioning is increased by adding ligands with affinity

    報道了由正負離子表面活性劑與高聚物混合溶液形成的一種可用於蛋白質的分離及分析的新型雙水相萃取體系.研究了正負離子表面活性劑（溴化十二烷基三乙銨/十二烷基硫酸鈉）分別與葡聚糖和聚乙二醇混合雙水相體系的形成規律、相行為及牛血清蛋白和溶菌酶在雙水相體系中的分配.通過在高聚物分子中接上親和配基，研究蛋白質在雙水相體系中的親和分配.結果表明，在該體系中，表面活性劑與高聚物分別富集於不同相中.升高溫度及加入無機鹽均可促進雙水相體系的形成，不同蛋白質可分配于不同的相中.親和配基的引入極大地增強了蛋白質分配的選擇性
  17. The reults of sds - page and western blot dermonstrated that the insoulable component of the induced e. coli culture contained protein 3a. the results of the study indicated that protein 3a existed in the form of inclusion body. the content of the expressed protein in the induced bacteria protein was 29. 2 % and 22. 1 % respectively

    Sds - page和westernbolt結果證實，大腸桿菌菌體不可溶性蛋白中富含3a蛋白，且此融合蛋白的分子量符合預期設計，說明3a蛋白在表達產物中以包涵體的形式存在，所表達的蛋白含量分別占菌體蛋白的29 . 2和22 . 1 。
  18. After the acet is vaporized, the active substance in water is gotten. and which is vaporized at low temperature. then the crude active substance is purified by column chromatography on sephadex g - 75. after a series of purifications again, we could get some white powder at last. though the active substance is diluted to50 g / ml, the activity is still checkeded - up through phyto phtnora casicileon. the purified active substance is insensitive to heat, resistant to chloroform 、 ethanol and the orhers. in addition, the active substance is sensitive to high ph ( 10 ~ 14 ), but it is not sensitive to low ph ( 1 ~ 5 ). furthermre, when the ph is made to low again, the activity of it ' s comes back

    用蒸餾水對菌體稀釋；加入適量吸附樹脂在150rpm 、 28下振蕩吸附4h ， 80 %的丙酮解吸，過濾解吸液得到活性物質的澄清溶液，旋轉蒸發儀旋轉蒸發去處丙酮，經sephadexg - 75分子篩層析得單一活性峰，收集峰值部分樣品液經冷凍乾燥得到淡褐色粉末，該活性物質用丙酮充分洗滌、甲醇-乙醚重結晶獲得略帶微黃的白色粉末，該活性物質50 g / ml仍可對蘇雲金芽孢桿菌hd - 1產生明顯的抑制作用。
  19. Acid protease gave play to synergetic action in liquor fermentation manifested as dissolving the granules of fermentation materials, advancing microbial propagation, decomposing protein to produce flavoring materials, and degrading yeast tropina

    摘要酒用酸性蛋白酶在白酒釀造的發酵過程中起協同作用，具有溶解發酵原料的顆粒、促進微生物繁殖、分解蛋白質生成香味物質、降解酵母菌體蛋白等多種功能。
  20. The aggregate of egg white lysozyme molecules formed during the refolding procedure of denatured - reduced egg white lysozymes was analyzed by protein electrophoreses and high - performance size - exclusion chromatography

    本文利用蛋白電泳和高效凝膠排阻層析法分析了還原脈變性蛋白溶菌酶稀釋復性過程中的集聚體。
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