protein biosynthesis 中文意思是什麼

protein biosynthesis 解釋
蛋白生物合成
  • protein : n. 【化學】朊，蛋白（質）。
  • biosynthesis : n. 生物合成。adj. -thetic ,-thetically adv.
  1. The global regulator csra of e. coli is a specific mrna - binding protein. csra negatively regulates several metabolic pathways that are induced post - exponentially, including glycogen biosynthesis, gluconeogenesis, and glycogen catabolism ; positively controls gene expression within the glycolytic pathway ; and also csra modulates the levels of enzymes that participate directly in pep metabolism

    Csra是整體調控網路的調控基因，可負調控指數生長後期誘導的一些代謝途徑，包括糖原的生物合成、糖原的分解代謝、糖異生，而對糖酵解的一些重要基因的表達則執行正調控功能， csra也調控直接參與pep代謝的三個酶的活性水平。
  2. It was suggested that the gene t13m11. 8 could be the ast candidate gene. this gene was 1432bp long with 6 exons and 5 introns. the putative protein of t13m11. 8 gene was highly homologous to dihydroflavonol 4 - reductase ( dfr ), which was an important enzyme in the anthocyanin biosynthesis pathway

    該基因的dna序列長1432bp ，含有6個外顯子和5個內含子，編碼的蛋白與花青苷生物合成途徑中的二氫黃酮醇4 -還原酶有較高的同源性。
  3. The protein encoded by orf1 show strong homology with cation efflux family protein from geobacter sulfurreducens pca [ identities = 65 / 272 ( 23 % ) ], and contains mmt1 - like putative conserved domains kog1485, mmt1 contains conserved domains kog1485 is mitochondrial fe2 + transporter ( cation diffusion facilitator superfamily ). so it can be considered that the protein encoded by o rf1 is fe2 + transporter involved in magnetosome biosynthesis in magnetospirillum gryphiswaldense msr - 1

    經同源比較和保守性結構域分析，推測orf1編碼的蛋白具有fe ~ （ 2 + ）轉運功能，在磁小體合成過程中將細胞質中fe ~ （ 2 + ）轉運到磁小體囊泡中，合成磁小體的同時去除fe ~ （ 2 + ）對細胞的毒害作用。
  4. The tn5 inserted in the orf4. it was demonstrated that this fragment was related to magnetosome biosynthesis by experiment of functional complement. the orf4 encodes a protein which is homologous to the atpase from magnetospirillum magnetotacticum ms - 1 and contains a rec domain which has a chey - homologous receiver domain

    該片段由6個orf組成， tn5插入在3621bp - 3622bp間，位於orf4起始密碼子下游的84bp處， orf4因tn5插入失活，通過功能互補實驗證明該片段與磁小體合成相關。
  5. P70s6k can regulate stop mrnas through s6 protein. cdc2 can inhibit p70s6k to decrease the translation of stop mrnas, and then the biosynthesis is controlled

    Cdc2在細胞分裂的過程中可以通過抑制p ~ （ 70 ） s6k來減弱具有5 top的mrnas的翻譯，進而抑制合成代謝。
  6. On d2 after attachment, the protein bands attained 23. after mating, the protein bands reached 26 and maintained the same until d4 after engorgement. these results meant that feeding and mating stimulated the biosynthesis of new protein

    饑餓雌蟲唾液腺有17條蛋白帶：吸血后2d增加到23條；交配后達到26條，直到飽血后4d保持不變，吸血和交配能刺激新蛋白的合成。
  7. The structure of ai - 2 has recently been elucidated and its biosynthesis depends on luxs protein

    Ai - 2的結構和生物合成途徑已被確定，其產生依賴于luxs蛋白。
  8. This domain receives the signal from the sensor partner in bacterial two - component systems. these results indicated that the protein of the orf4 works as atpase function involved in the synthesis of magnetosome or takes part in the signal transduction relate to the promotion of magnetosome biosynthesis

    通過對orf4編碼蛋白同源比較和功能分析，推測orf4編碼蛋白可能的功能有兩種：具atpase活性，在磁小體合成過程中為鐵轉運提供能量；或參與磁小體合成啟動過程中的信號轉導。
  9. Hisityl - trna synthetase catalyzes the aminoacylation of trnahis in the initial step of protein biosynthesis. the involumen of histidyl - trna synthetase in autoimmune diseases is another feature of the enzyme. in studies, it is reported that purified jo - 1 antigen can increase the detection rate of anti - jo - 1 antibody. but it is difficult to obtain a single component by biochemical extraction. genetic engineering can help us to desolve this problem. after looking up mrna sequence encoding histidyl - trna synthetase in genebank, we used rt - pcr technology to gain its full length dna sequence. the vestor ptybllwas used in the construction of expressing vestor. we transformed the jo - 1 gene into er2566 and used this system to express fusion jo - 1 antigen

    本實驗從人胎盤中提取總rna ，利用rt - pcr技術獲得了編碼jo - 1的基因整長序列，選用impact - cn系統中的ptyb11載體，構建了jo - 1基因的克隆與表達載體，並轉化大腸桿菌er2566 ，經過抗性篩選、分子量大小比較、雙酶切鑒定、和pcr鑒定等多種方法驗證，篩選出了5個陽性克隆。
  10. Study on incorporation activity of 3h - glycine into protein biosynthesis of silkworm, bombyx mori

    對家蠶蛋白質生物合成參入活性的研究
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