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1,5-脱水-D-果糖及其衍生物:生物合成、制备和潜在的医学应用。

1,5-anhydro-D-fructose and its derivatives: biosynthesis, preparation and potential medical applications.

机构信息

Department of Medicine, Unit of Emergency Medicine, Karolinska Institute, Huddinge, Stockholm, Sweden.

出版信息

Planta Med. 2010 Oct;76(15):1635-41. doi: 10.1055/s-0030-1250120. Epub 2010 Jul 19.

DOI:10.1055/s-0030-1250120
PMID:20645241
Abstract

1,5-Anhydro-D-fructose (AF) was first found in fungi and red algae. It is produced by the degradation of glycogen, starch and maltosaccharides with α-1,4-glucan lyase (EC 4.2.2.13). In vivo, AF is metabolized to 1,5-anhydro-D-glucitol (AG), ascopyrone P (APP), microthecin and other derivatives via the anhydrofructose pathway. The genes coding for the enzymes in this pathway have been cloned, enabling the large-scale production of AF and related products in a cell-free reactor. The possible applications of these products in medicine have been evaluated using both in vitro and in vivo systems. Thus AF is a useful anticariogenic agent as it inhibits the growth of the oral pathogen Streptococcus mutans, impairing the production of plaque-forming polysaccharides and lactic acid. AF also shows anti-inflammatory and anticancer effects. AG is used as a diabetic marker for glycemic control. AG also stimulates insulin secretion in insulinoma cell lines. in vivo, APP has been shown to lengthen the life span of cancer-afflicted mice. It interferes with tumor growth and metastasis by its cidal effects on fast multiplying cells. Microthecin inhibits the growth of the human pathogen Pseudomonas aeruginosa PAO1, particularly under anaerobic conditions. The pharmaceutical usefulness of the other AF metabolites 1,5-anhydro-D-mannitol,1-deoxymannojirimycin, haliclonol, 5-epipentenomycin I, bissetone, palythazine, isopalythazine, and clavulazine remains to be investigated. In this review AF and its metabolites as the bioactive natural products for their pharmaceutical potentials are discussed.

摘要

1,5-脱水-D-呋喃果糖 (AF) 最初在真菌和红藻中发现。它是通过α-1,4-葡聚糖裂解酶 (EC 4.2.2.13) 降解糖原、淀粉和麦芽糖产生的。在体内,AF 通过脱水果糖途径代谢为 1,5-脱水-D-山梨糖醇 (AG)、阿朴吡喃酮 P (APP)、微他西和其他衍生物。该途径中酶的编码基因已被克隆,使 AF 和相关产品能够在无细胞反应器中大规模生产。这些产品在医学上的可能应用已通过体外和体内系统进行了评估。因此,AF 是一种有用的抗龋齿剂,因为它可以抑制口腔病原体变形链球菌的生长,从而破坏菌斑形成多糖和乳酸的产生。AF 还具有抗炎和抗癌作用。AG 用作血糖控制的糖尿病标志物。AG 还刺激胰岛素瘤细胞系胰岛素的分泌。在体内,APP 已被证明可以延长癌症小鼠的寿命。它通过对快速增殖细胞的杀伤作用干扰肿瘤生长和转移。微他西抑制人类病原体铜绿假单胞菌 PAO1 的生长,特别是在厌氧条件下。其他 AF 代谢物 1,5-脱水-D-甘露醇、1-去氧甘露糖基肌氨酸、海立克酮、5-表戊烯霉素 I、比塞酮、普洛替嗪、异普洛替嗪和克拉维嗪的药用价值仍有待研究。在这篇综述中,讨论了 AF 及其代谢物作为具有药物潜力的生物活性天然产物。

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