納豆激酶 的英文怎麼說
中文拼音 [nàdòujī]
納豆激酶
英文
nattokinase-
Research of the mechanism of nattokinase biosynthesis
納豆激酶的合成機制Finally, the anion exchanger was used to recover dehalogenase from unclarified cell homogenate, while the cation exchanger was introduced to purify nattokinase directly from fermentation broth
最後，所開發的陰離子吸附劑被應用於從細胞勻漿中提取脫鹵酶，而陽離子交換劑則被用來從發酵液中提純納豆激酶。The separation of nattokinase in leavening agent
發酵液中納豆激酶鹽析法分離的研究Study on pepsin ' s chemical modification of nattokinase
胃蛋白酶對納豆激酶的化學修飾研究An assay method for thrombolysis activity of nattokinase
納豆激酶溶栓活性的測定方法Comparison on nattokinase activity detecting method
納豆激酶活性測定方法的比較Research advancement of nattokinase gene engineering
納豆激酶基因工程研究進展Advances in research on thrombolysis mechanism of nattokinase
納豆激酶溶解血栓機制Study on metal ion chemical modification of nattokinase
金屬離子對納豆激酶的化學修飾研究Nattokinase ( nk ) is a new fibrinolytic enzyme which cleaves directly cross - linked fibrin in vitro / in vivo
納豆激酶是一種能夠在體內及體外直接分解交聯纖維蛋白的新型溶血栓酶。Research status and prospects about nattokinase
納豆激酶的保健功能及分離提取技術研究Expression and purification of nattokinase gene
納豆激酶基因的表達及純化As a serine proteases, the expression product was detected with a relatively high protease activity. a similar result was also obtained from fibrin plate assay, it reveal ed that the expressed nk was provided with fibrinolytic activity
由於納豆激酶是一種蛋白酶，我們首先檢測並發現表達產物具有蛋白酶活性，通過纖維蛋白平板檢測表達產物具有溶圈活性，表明表達的納豆激酶具有溶解血栓的生物學功能。Studies on the liquid fermentation for nattokinase by bacillus natto
納豆菌液體發酵生產納豆激酶的研究Study on the optimization of nattokinase liquid fermentation by bacillus natto
納豆激酶液體發酵條件研究Then bm cell line was co - transfected with parental bm - npv dna and the transfer plasmid pvl - nk, the recombinant virus was then obtained subsequently with routine procedure. nattokinase was expressed in silkworm larva by injection with the recombinant virus
將nk基因克隆至轉移載體pvl - 1393中後用常規方法獲得重組病毒，感染家蠶后納豆激酶獲得正確表達。The crafts of making sa / cs - cacl2 / pmcg capsule was introduced. the effects of pmcg on the growth of bacillus subtilis and was studied. and we also studied the difference of microencapsulated cell and free cell on growth rate, consuming rate of xylose and producing rate of notokinase and we got high activity of enzyme after 6 batches culture
詳細的介紹了sa / nacs - cacl _ 2 / pmcg微膠囊的制備過程，考察了pmcg對枯草桿菌生長的影響，並考察了微膠囊培養與游離培養在菌體生長和耗糖速率，以及納豆激酶產物分泌上的區別。Dna sequence analysis showed that the cloned nk gene was highly homologous to the sequence reported by nakamura. the deduced amino acid sequence also had the conserved sequences ( serine 221, histidine 64, and aspartic acid 32 ) which was essential for the catalytic center of serine proteases. the nk gene was then cloned into the transfer vector pvl1393
本實驗以b . subtilis （ natto ）基因組dna為模板擴增了nk基因，測序結果顯示與nakamura報道的納豆激酶基因高度同源，其氨基酸序列也含有絲氨酸蛋白酶的活性保守中心（ serine221 ， histidine64 ， asparticacid32 ） 。Study of liquid fermentation conditions optimization on nattokinase
納豆激酶液體發酵條件的優化研究分享友人