鞭毛基體 的英文怎麼說
中文拼音 [biānmáojītǐ]
鞭毛基體
英文
flagellar basal body-
Microtubules are also used in the construction of centrioles, basal bodies, cilia and flagella.
微管還用於建造中心粒，基體，纖毛和鞭毛。Flagellum ( pl. flagella ) a whiplike extension of prokaryote cells, with a basal body at its base, whose beat causes locomotion of the cell
鞭毛：原核細胞的鞭狀延長部分，基部有基體，當鞭毛進行揮鞭式運動時可以促使細胞移動。The number of species of kinetoplastida and amoebida occupied a dominant position respectively in mastigophora and sarcodina
鞭毛亞門以動基體目的物種占優勢，肉足亞門以變形目的物種占優勢。It is believed that it can bring the important inspiration for the future medical micro robot which can be embedded into inner organ of human for inspection, drug spot deliverance and local body surgery. supported by supported by the nation nature science foundation of mechanism, structure and control study on swimming micro robot in liquid ( item no. 69885002 ) and guangdong province science foundation of research on swimming micro robot in liquid ( item no. 980402 ) and guangdong province education department foundation of research on micro pipe robot driven by liquid self energy ( item no. 010043 ), this dissertation mainly deals with much theoretical and, including research situation and the main issue of micro mobile robot in liquid, fish propulsion mechanism, design and locomotion mechanism, and flagellum - like propulsion swimming micro robot in low reynolds number viscous liquid
本論文得到國家自然科學基金項目「泳動微機器人的機理、機構和控制」 （項目資助號： 69885002 ） 、廣東省自然科學基金項目「液體中泳動微機器人的研究」 （項目資助號： 980402 ）和廣東省教育廳基金項目「基於流體自身能量的微管道機器人研究」 （項目資助號： 010043 ）的資助，主要對液體中微機器人的國內外研究現狀和主要研究問題、魚類推進機理、液體中微機器人的設計與運動機理、低雷諾數粘性液體中仿鞭毛推進微機器人研究等方面進行了大量的理論與實驗研究。With bacterial cgc as main subject, the tests had been done to elucidate mechanism of self - organization for macroscopic rhythmic structure. the dynamics of cgc forming was observed by special techniques of waving culture and microscopic culture ; the differences in outer structure of cell wall and flagella number had been observed by atomic force microscope scanning ; integrity of cell wall was examined under tem ; outer membrane protein was analysed by sds - page and various substance and factors for cgc formation were determined
採用特殊的波動培養和顯微培養技術觀察潛生體形成動態；應用原子力顯微鏡掃描，比較細菌潛生體與繁殖體在細胞壁外層結構和鞭毛數量的差別；用透射電鏡觀察細胞壁完整性，以十二烷基硫酸鈉?聚丙烯酰胺凝膠電泳分析外膜蛋白的改變，並通過實驗分析多種物質和因素對潛生體形成的影響。分享友人