| DC 欄位 |
值 |
語言 |
| DC.contributor | 化學學系 | zh_TW |
| DC.creator | 林運旺 | zh_TW |
| DC.creator | Yun-Wang Lin | en_US |
| dc.date.accessioned | 2020-7-30T07:39:07Z | |
| dc.date.available | 2020-7-30T07:39:07Z | |
| dc.date.issued | 2020 | |
| dc.identifier.uri | http://ir.lib.ncu.edu.tw:444/thesis/view_etd.asp?URN=107223039 | |
| dc.contributor.department | 化學學系 | zh_TW |
| DC.description | 國立中央大學 | zh_TW |
| DC.description | National Central University | en_US |
| dc.description.abstract | Pseudaminic acid是一種唾液酸的衍生物，也是許多革蘭氏陰性菌細胞表面的醣聚合物的成分之一。不同革蘭氏陰性菌的細胞表面，有些含有pseudaminic acid，有些則是含有pseudaminic acid的衍生物，而衍生物就是原本pseudaminic acid的架構在碳五或碳七的胺基上做不同的官能基改變。許多研究指出pseudaminic acid與細菌是否能感染宿主細胞因而致病有關，而常見的革蘭氏陰性菌例如:大腸桿菌、弧菌、綠膿桿菌…等。這些革蘭氏陰性菌都具有致病性，並且對人體有害，而大多數的抗生素都不能有效抑制此類細菌，所以對於pseudaminic acid在感染宿主機制上所扮演的角色的研究是非常重要的，但由於目前無法藉由培養細菌大量純化取得pseudaminic acid，因此如何以人工合成pseudaminic acid便顯得十分重要，有鑑於現行發表的數種合成方法有著低總產率及步驟繁複等缺點。在本論文中，我們設計了新的合成路徑，除了能使用較便宜的D-glucosamine和L-ascorbic acid (俗稱維他命C)作為起始物，還能在較少合成的步驟中能將pseudaminic acid的碳五與碳七位置上的疊氮選擇以不同官能基去修飾，形成不同胺的官能基，這對於在pseudaminic acid及相關衍生物的合成是尤為重要的。 | zh_TW |
| dc.description.abstract | The nonulosonic acid class of sugars consists of 9-carbon α-keto acid carbohydrate monomers. Unique to bacterial species are the recently identified sialic acid derivatives, which are an important sub-class of nonulosonic acids. Pseudaminic acid and legionaminic acid occur as several derivatives with changes in the nature of the amide groups attached to C-5 and C-7. Pseudaminic acid with the L-glycero-L-manno configuration differs from sialic acid in configuration at both the C-5 and C-7 positions in addition to the deoxygenation at C-9 and the N for O substitution at C-7. Pseudaminic acid is found coating the surface of various bacterial human pathogens. Protein glycosylation is an essential post-translational modification in bacteria that has emerged as a new entry to study bacterial pathogenesis and develop novel therapeutic intervention. In particular, Pseudaminylation of proteins has been the subject of significant interest owing to their importance in Gram-negative bacterial pathogens. To date, several synthetic routes have been reported to synthesize pseudaminic acid and its derivatives. All these efforts resulted in poor overall yield and low stereo- and regioselectivity through a number of steps total synthesis. Herein we present two facile de novo synthetic routes toward pseudaminic acid and its functionalized derivatives from easily available D-glucosamine and L-ascorbic acid (vitamin C), respectively. The key reactions in our de novo synthesis involve the diastereoselective azide-based SN2 reaction to create the 2,4-anti-diamino skeleton, followed by the reduction and aldol-type allylation. | en_US |
| DC.subject | 革蘭氏陰性菌 | zh_TW |
| DC.subject | 醣聚合物 | zh_TW |
| DC.subject | Pseudaminic acid | en_US |
| DC.subject | nonulosonic acid | en_US |
| DC.title | 從葡萄糖胺及抗壞血酸合理設計合成細菌特有單醣:偽胺基酸 | zh_TW |
| dc.language.iso | zh-TW | zh-TW |
| DC.title | Rational Design and Synthesis of Bacterial Specific Monosaccharide: Pseudaminic Acid from D-Glucosamine and L-Ascorbic Acid | en_US |
| DC.type | 博碩士論文 | zh_TW |
| DC.type | thesis | en_US |
| DC.publisher | National Central University | en_US |