膜囊類 的英文怎麼說

中文拼音 [mónánglèi]
膜囊類 英文
dinocapsae
  • 膜 : 名詞1. [生物學] （像薄皮的組織） membrane 2. （像膜的薄皮） film; thin coating
  • 囊 : 囊名詞1. （口袋） bag; pocket; sack; purse 2. （像口袋的東西） anything shaped like a bag 1. （姓氏） a surname
  • 類 : Ⅰ名1 （許多相似或相同的事物的綜合; 種類） class; category; kind; type 2 （姓氏） a surname Ⅱ動詞...
  1. Using templates is an important method to regulate and control the morphology and size of crystal. according to the characterization of templates and the ability of their domain limitation, template methods were divided into two parts, hard - template methods and soft - template methods. soft - template methods mainly included many kinds ordered congeries that composed by amphiphathic molecules, such as liquid crystal, colloid, microemulsion, vesicle, lb films, self - assemble films, and so on, the self - assemble structure of macromolecules and biomacromolecules was also included

    模板法是對晶體的形貌和尺寸進行控制的一類重要的方法，根據模板自身的特點和限域能力的不同分為硬模板和軟模板，軟模板主要包括兩親分子形成的各種有序聚合物，如液晶、膠團、微乳狀液、囊泡、 lb膜、自組裝膜等，以及高分子的自組織結構和生物大分子等。
  2. At low concentration of zn, the changes in ultrastructure were nuclei deformation, chloroplast swelling and disorder of thylakoid arrangement ; serious damages in ultrastructure caused by greater zn stress were indicated by scattered nucleoli, condensed chromatin, almost empty nuclei with nuclear membrane disrupted and nucleoplasm flowing into cytoplasm, swollen and partly dissolved cristae of mitochondria, disrupted and collapsed chloroplast envelopes, and some dissolved thylakoids that flew into cytoplasm

    超微結構的變化也呈現加重趨勢，低濃度處理的變化為細胞核變形、葉綠體膨脹、類囊體排列紊亂；嚴重的超微結構的損傷是核仁散開、染色質凝集，細胞核幾乎成為空核和核膜破裂，核質散出；線粒體脊突膨脹和部分溶解；葉綠體膜斷裂、消失和部分類囊體溶解和散到細胞質中。
  3. In a series of 30 cases of retinitis pigmentosa, pigment epithelial alterations included mottling of the macula in 8 eyes ( 13. 3 % ), bull ' s - eye pattern in 24 eyes ( 40 % ) and atrophy or hypopigmentation in 56 eyes ( 93. 3 % ) ; macular edema with retinal thickening was present in 30 eyes ( 50 % ), cystoid macular edema in 18 eyes ( 30 % ) ; broadening or loss of foveal reflex was present in 60 eyes ( 100 % ), preretinal membrane noticed in 58 eyes ( 96. 7 % ) and macular hemorrhage in one eye ( 1. 7 % )

    摘要對網膜色素變性癥的病例30例60眼探討其黃斑部病灶的情形，網膜色素上皮層變化中的雜色斑點病變見於8眼，頻率為13 . 3 % ，牛眼樣病灶見於24眼（ 40 % ） ，網膜脫色素病灶為56眼（ 93 . 3 % ） ；黃斑部浮腫之網膜增厚為30眼（ 50 % ） ，類囊胞浮腫為18眼（ 30 % ） ；其它變化包括中心窩反射消失或增寬為60眼（ 100 % ） ，網膜前纖維膜為58眼（ 96 . 7 % ） ，黃斑部出血和疑似網膜下新生血管各為1眼（ 1 . 7 % ） 。
  4. Influence of some factors on the fluorescence characterization of phosphatase in the thylakoid membrane of ipomoea aquatica

    金屬離子等因素對蕹菜類囊體膜蛋白磷酸酯酶熒光性質的影響
  5. This enzyme was different with the ones reported in the past. a phosphatase was isolated from the chloroplast thylakoid membrane of ipomoea aquatica, by nacl extration, ammonium sulfate precipitation, ion - exchange chromatography and hydrophic chromatography through butyl - toyopearl 650m column

    使用nacl抽提、硫酸銨分步沉澱、離子交換和butyl - toyopearl650m疏水柱層析等方法，從蕹菜葉綠體類囊體膜中分離純化到一種蛋白磷酸酯酶。
  6. For uncovering the effects of reversible phospharylation on the structure and function of psii reaction centre, we purified a protein phosphatase associated membrane from the thykaloid membrane of ipomoea aquatica chloroplasts. in our experiments we studied the enzymology and spect rum characters of the purified phosphatase. in our lab, one kind of protein phosphatase associated thylakoid membrane of pomoea aquatica has been isolated

    迄今人們對類囊體蛋白磷酸酯酶的研究較少，為了研究可逆磷酸化對psii反應中心結構與功能的影響，本文以蕹菜為材料，從葉綠體類囊體膜中分離純化到一種膜結合蛋白磷酸酯酶，進行了酶學性質和光譜性質的研究。
  7. Periodically, the lamellae become enlarged, forming flattened, membrane-enclosed vesicles called thylakoids.

    片層周期性地擴展，形成扁平的有膜為界的囊，稱為類囊體。
  8. Recovery of this photoinhibition is a complicate but orderly course, including degradation of photodamaged d1, synthesis and assembly of new one, etc. using lincomycin to block the replacement of new synthetic dl protein into photodamaged one, the spinach leaves was exposed to highlight, giving rise to photoinhibition before the thylakiod membranes were isolated

    解除光抑制后， ps活性恢復是一個復雜而有序的過程，需要d1蛋白降解、新合成d1蛋白和重組裝ps等。實驗首先進行菠菜葉片光抑制處理，加入林可黴素阻斷葉綠體蛋白質合成，利用尿素sds變性電泳分離類囊體膜蛋白，藉助d1蛋白抗體westen免疫印跡、磷酸化蛋白快速檢測方法分析d1蛋白存在形式，並進行定量分析。
  9. Chloroplast phosphoprotein were first found in thylakoid membranes by bennett o the attachment or removal of a phosphate group from a protein may have profound effects on that protein ' s activities and properties, the reversible phospharylation of the membrane protein in thykaloid is a dymanic equilibrium process

    而bennett （ 1977 ）發現的類囊體膜蛋白可逆磷酸化已成為近年研究的熱點之一，蛋白質連上或是移去磷酸基團都將強烈影響蛋白質的生理活性和性質，這需要類囊體膜蛋白激酶和磷酸酯酶的參與。
  10. The degree of saturation of fatty acids has been measured for thylakoid membranes isolated from leaves of common beans differing in heat tolerance and grown under optimal and high temperature

    摘要以耐熱性不同的菜豆品種為材料，研究高溫脅迫下類囊體膜脂脂肪酸組成及飽和度的變化。
  11. These results suggest that the cytoplasmic dynein intermediate chain - like protein exists in lily pollen, and it distributes mainly on either cis - and trans - golgi - associated vesciles

    以上的結果表明類細胞質力蛋白中間鏈存在於百合花粉及花粉管中，並且在百合花粉管中順面和反面高爾基體附近的囊泡膜上均有分佈。
  12. By sds - page and immuno - blotting, the monoclonal antibody of anti - chick brain cytoplasmic dynein intermediate chain could recognize the 67 kda protein in purified golgi apparatus fraction from lily pollen. subsequently by immuno - gold labeling and transmission electron microscopy, we found that the dynein intermediate chain - like protein bound mainly to the membranes of golgi - associated vesicles. statistics analysis of dynein intermediate chain - like protein on golgi - associated vesciles showed the nearly equal chance of distribution on either cis - or trans - golgi - associated vesciles

    對分離純化的百合花粉及花粉管中高爾基體組分進行sds -聚丙烯酰胺凝膠電泳和免疫印跡發現，抗雞腦細胞質力蛋白中間鏈單克隆抗體在67kda處有較強的免疫交叉反應；進而通過免疫金標結合電子顯微鏡觀察發現，大多數類細胞質力蛋白中間鏈存在於高爾基體附近的囊泡膜上；統計結果表明，類細胞質力蛋白中間鏈在順面和反面高爾基體附近囊泡膜上的分佈機率大致相等。
  13. In this report, we mainly covered the following aspects of " tissue organ regeneration and replication in situ " : 1 ) procedures of tissue organd regeneration and replication and replication in clnical practice ; 2 ) the discover and existence of potentiald regenerative cell ( prc ) ; 3 ) the proliferation, differentiation and regeneration law of potential law of potential regenerative cells ; 4 ) study procedure on tissue organ regeneration and replication from prcs in vitro based on the model of full skin organ regeneration in situ after extensive in vitro, set up the method and technology of searching life regenerative substance required in tissue organ regeneration and replication in situ. in this study, first, the whole human body is divided into 206 function units, which are the " tissue organ " in regeneration study. then the histology foundation of tissue organ regeneration and replication in situ is set up. in ordre to prove the existence of the potential regenerative cells and their potential baility and function, we established clinical tracking rechnique of skin organ regeneration in situ ; meanwhile, several tissue organ regeneration and replication in vitro models which represent different kinds of runctions were sucessfully set up, with all these techniques and models, we confirmed : 1 ) the existence, function and ability of pptemtoa regenerative cells ; 2 ) the importance of life regenerative substance ; 3 ) the feasibility of tissue organ regeneration and replication in situ ; 4 ) the big value of tissue organ regeneration and replication in situ in life science and medicine progerss. we also showed the possible foreground of capture cancer with this method and technologh. in this report, nearly 200 photographs of several tissue organ regeneration and replication in situ or in vitro demonstrated the whole process of tissue organ and big organ entities regeneration and replication from cells. the results of tissue organ regeneration and replication in situ mainly include : 1 ) whole skin organ regeneration and replication in situ ; 2 ) gastrointestinal mucosa tissue organ regeneration in vitro ; 3 ) hair follicle tissue organ regeneration in situ or in vitro ; 4 ) never tissue organ regeneration in situ ; 5 ) pancreas tissue organ regeneration and replication in vitro ; 5 ) marrow tissue regeneration in vitro ; 6 ) renal glomerulus and tubule tissue organ tugeneraation in vitro ; 7 ) heart muscle regeneration in vitro, etcl. in order to let more and more people know and understand this technology of tissue organd regeneration and replication in situ, herein, for the first time, we publicize the key points of actualizing this technology. also, we publicized the technology procedures and the frame constitute of life substances. we bilieve this is a big contribution to human science

    本研究報告，重點報道了組織器官的原位再生復制的臨床程序，報道了組織潛能再生細胞的發現和存在，以及該細胞的增殖分化和形成組織器官的變化規律.以燒傷后皮膚組織器官的原位再生復制為模型，研究出了體外組織潛能再生細胞復制組織器官的培養方法;以體外組織器官的復制為模型，建立了尋找原位組織器官再生復制所需生命物質的方法和技術.本研究，首先按人體的器官功能，分解為206個功能單位，確立了所復制的人體器官中的組織功能單位為組織器官，從而建立了原位組織器官再生復制的組織學基礎.為了驗證組織潛能再生細胞的再生潛能，建立了皮膚器官原位再生的實體臨床跟蹤技術，同時又建立了能代表有關器官功能類別的代表組織器官的原位和體外復制模型，以多組織器官的成功復制確定潛能再生細胞的作用，確定生命研究再生物質的重要性，確定組織器官原位再生復制的可行性，確定了組織器官原位再生復制的生命科學研究和醫學進步的重大應用價值，同時展示了用此方法和技術攻克癌癥的前景.本研究報告，以近二百幅多個組織器官原位和體外再生復制的實體圖片，展示了潛能再生細胞復制的組織器官和大器官司實體;展示了細胞再生復制器官的全過程.真實的報告了組織器官原位再生復制的成果.所公布的主要成果為:皮膚器官的原位再生復制;胃腸黏膜組織器官的原位和體外再生復制;毛囊組織器官的原位和體外再生復制;神經組織器官的原位復制;胰腺組織器官的體外復制;骨髓組織的體外復制;腎小球小管組織器官的體外復制;心肌的體外復制等.為了讓更多的人學會和掌握組織器官原位再生復制技術，本報告首次公布實施技術的重要環節和技術流程;首次公布了生命再生物質的框架和組成.作者自費研究成果對人類生命科學的一大貢獻
  14. In addition to iel, two types of intraepithelial plasma cells were observed in the intestinal mucous epithelium. one type was with dilated rough endoplasmic reticulum ( rer ) and the other was

    在腸粘膜上皮內，除iel外，作者還觀察到兩種類型的上皮內漿細胞，一種為粗面內質網擴張型；另一種為粗面內質網扁囊板層型，提示鱉的粘膜免疫具有一定特殊性。
  15. Psii consists of more than 20 different subunits, most of them being integral membrane proteins, mediating the electron transfer chain. so revealing the organization of psii subunits is a key point to elucide the mechanism of psii function

    Ps的各蛋白組分有序地排列在類囊體膜上，通過其結合的輔因子形成了獨特的電子傳遞和水裂解體系。
  16. The results showed that the lumen of small intestine was lined by the simple columnar epithelium, most of the cells were high columnar absorbing ones with abundant developed microvilli

    結果表明，中華鱉小腸黏膜上皮為單層柱狀上皮，以高柱狀吸收細胞為主，具有發達的微絨毛、線粒體、粗面內質網和膜包小囊泡，其結構的發達程度已接近高等哺乳動物和鳥類。
  17. In higher salinity ( 200, 400mm ) the lamellae expanded remarkably, the membrane of the chloroplast was broken, some crystallinity was found in some chloroplast. there is also some compound vesicular structure in the mesophyll cells under salt stress. the results were discussed with regard to the mechanism by which the vesicular structure was produced

    200mm有些葉綠體中被膜破碎，基粒、基質片層界限非常混亂，類囊體結構扭曲，排列雜亂，澱粉粒輪廓模糊，有些葉綠體被膜向外突出，形成管泡狀結構。
  18. The fluorescence spectra of brown algae thylakoid membrane and ps i complex varied from higher plants, they had no fluorescence emission maximum at 730 nm. we concluded that 730 nm fluorescence was no more a symbol of ps i

    在裙帶菜純化的類囊體膜和ps復合物的熒光光譜中，均未發現屬于ps的730nm的熒光發射峰，指出730nm熒光峰不能作為ps的表徵。
  19. From above, we indicate that : photoinhibition cause chlorophyll an " bleak " while influorecsence of proteins on thylakiod membrances has no prominent response to it. what ' s more, photoinhibiton induce d1 protein phosphorylated and aggregated, forming the aggregators with phosphorylated d1

    結果表明：光抑制對葉綠素熒光具有漂白作用，對類囊體膜蛋白內源熒光無明顯影響；光抑制處理引起d1蛋白磷酸化並發生聚合，且聚合物中d1蛋白以磷酸化形式存在。
  20. The culture supernatants of heat - shocked and control a20 cells were collected to isolate exosomes through a sequence of differential centrifugation steps. briefly, cells were removed by centrifugation for 5 min at 300x gmax

    在透射電鏡下hs一exo形態與exo類似，呈50一sonm的雙層膜囊泡樣結構，大小比較均一，結構完整。
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