類囊體基質 的英文怎麼說
中文拼音 [lèinángtǐjīzhí]
類囊體基質
英文
stroma thylakoid-
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。These stacks of thylakoids are called grana.
這些成堆的類囊體稱為質體基粒。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。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。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。Based on these observations, we isolated protoplasts from female germ unit and performed extracellular ca2 + influx experiment in order to check whether the cytological event similar to what happens during fertilization will be induced by extracellular ca2 + influx
表明細胞壁的合成是受精后早期發生的細胞學事件。在此基礎上，我們分離了胚囊細胞的原生質體。通過外源導入鈣離子檢查鈣能否引發類似受精過程發生的細胞學事件。Inside the chloroplast is a fluid called stroma, which contains a series of flattened stacks of thylakoids
葉綠體裏面是一種叫基質的液體，它含有一系列扁平的成堆的類囊體。In addition, at the ultrastructure scale, there are evident differences in chloroplast. in lower salinity ( 50, 100mm ), the lamellae of stoma and grana in some chloroplast expanded lightly ; the boundary of the chloroplast was dim
在50 、 100mhnacl處理下，細胞中有些葉綠體的基質、基粒片層稍有變形，被膜界限出現模糊現象，類囊體出現膨大。The observation by transmission electron microscope indicated that while a. vera l. had been shaded for six months, it showed decreased chloroplast grana and decreased and loosely arranged thylakoid lamellas in its leaf cells and the starch originally accumulated in its leaf plastids declined until it disappeared, presented such underdeveloped inner - membrane systems as endoplasmic reticula and golgiosomes
電鏡觀察結果表明，遮蔭處理6個月後，庫拉索蘆薈葉片細胞中葉綠體基粒數量減少，類囊體片層數目減少且排列疏鬆，質體中原來積累的澱粉粒逐漸減少直至消失；內質網、高爾基體等內膜系統不發達。分享友人