探討Neosartorya fischeri NRRL 181基因串的二次代謝產物

CNU IR > Pharmacy and Science > Dept. of Biotechnology (including master's program) > Dissertations and Theses > Item 310902800/26112

Please use this identifier to cite or link to this item: https://ir.cnu.edu.tw/handle/310902800/26112

Title:	探討Neosartorya fischeri NRRL 181基因串的二次代謝產物 Investigation of secondary metabolites of Neosartorya fischeri NRRL 181 gene cluster
Authors:	林函蓉
Contributors:	生物科技系暨研究所洪瑞祥
Keywords:	真菌 pH值 NRPS PKS Neosartorya fischeri fungus pH NaCl nkuAΔ
Date:	2012
Issue Date:	2012-11-29 11:35:51 (UTC+8)
Abstract:	真菌是一群多種型態的細胞，由菌絲組成的真核生物，其細胞壁構造與植物有明顯的差異，但缺乏葉綠素且無法行光合作用，屬異營性生物，其價值來自於二次代謝產物，到目前為止，此化合物應用於許多抗腫瘤、抗菌、及抗毒性的藥物，因此，在現今已被作為食品工業與醫藥用材之用途。過去文獻證實，真菌Neosartorya fischeri合成二次代謝產物的基因序列，有16組PKS與18組NRPS基因序列所調控。然而在過去研究顯示，Neosartorya fischeri所產生的二次代謝產物，目前只有三種化合物，代表尚有許多二次代謝產物還未被分離及鑑定。而在一般的實驗室培養條件下，Neosartorya fischeri有許多微量的二次代謝產物不容易被觀察，因此，我們想要嘗試以分子生物的技術或是透過不同配方的培養基獲得二次代謝產物。透過Fusion PCR技術，結果顯示，將Neosartorya fischeri NRRL181基因串進行融合，目前WA5’/NFIA_043640與NFIA_043650/NFIA_043660片段已融合完畢。而另一方面透過培養天數得知，培養20天二次代謝物訊號能增加，而透過不同配方的培養基，改變環境因子pH值，結果顯示，pH值越呈鹼性，20和22分鐘的二次代謝產物訊號，會明顯的增強;而環境因子滲透壓，結果顯示，當鹽濃度越來越高時，主要的20和22分鐘的二次代謝產物訊號，會越來越低。期望能透過Fusion PCR技術，將Neosartorya fischeri NRRL181基因串進行融合，送入帶有nkuAΔ這段可刪除基因的Aspergillus nidulans表現系統中;以及藉由HPLC觀察，進一步獲取大量的二次代謝產物並建立資料庫，以利未來在臨床醫學或藥物治療能有所貢獻或新的發展。 Fungi are a group of a variety of cell types, by the mycelium of eukaryotes, there are significant differences in their cell wall structure and plant, but the lack of chlorophyll and not conducted photosynthesis, belonging to the abnormal Camp biological, its value comes from the secondary metabolites, far the way, Application of many anti-tumor, anti-bacterial and anti-toxicity drugs, therefore, as has been the use of food industry and pharmaceutical materials. Literature confirmed that Neosartorya fischeri synthetic gene sequence of secondary metabolites, there are 16 groups of PKS and 18 groups NRPS gene sequence of the regulation. However, studies have shown that in the past, secondary metabolites produced by Neosartorya fischeri, currently only three kinds of compounds, representative there are many secondary metabolites has not yet been isolated and identification. In laboratory culture conditions, Neosartorya fischeri has trace amounts of secondary metabolites is not easy to be observed, therefore, we want to try to molecular biological techniques, or through the medium of different formulations of secondary metabolites.By Fusion PCR, The results showed that fusion of Neosartorya fischeri NRRL181 gene string, the WA5'/NFIA_043640 and NFIA_043650/NFIA_043660 fragment fusion is complete. On the other hand through learned through training days, training 20 days secondary metabolite signals can increase; through the medium of different formulations, changing environmental factors pH value, the results showed that pH values more alkaline, 20 and 22 minutes of secondary metabolites signal will be significantly enhanced;Osmotic pressure of environmental factors, results showed that, when the salt concentration is getting higher and higher, 20 and 22 minutes of the main secondary metabolites signal will be getting lower and lower. Expectations through Fusion PCR technique,fusion of Neosartorya fischeri NRRL181gene string, transformation with carry nkuAΔ delete the genes, of Aspergillus nidulans expression system, obtain many of secondary metabolites;And observed by HPLC, and further access to a large number of secondary metabolites and to create a database to facilitate future in clinical medicine or drug therapy can contribute to new development.
Relation:	校內一年後公開，校外永不公開，學年度：100，85頁
Appears in Collections:	[Dept. of Biotechnology (including master's program)] Dissertations and Theses

Files in This Item:

File	Description	Size	Format
index.html		0Kb	HTML	2027	View/Open

Loading...