Jankowska Dagmara A, Trautwein-Schult Anke, Cordes Arno, Bode Rüdiger, Baronian Keith, Kunze Gotthard
a Leibniz Institute of Plant Genetics and Crop Plant Research (IPK) ; Gatersleben , Germany.
Bioengineered. 2015;6(1):20-5. doi: 10.4161/21655979.2014.991667. Epub 2015 Jan 8.
The purine degradation pathway in humans ends with uric acid, which has low water solubility. When the production of uric acid is increased either by elevated purine intake or by impaired kidney function, uric acid will accumulate in the blood (hyperuricemia). This increases the risk of gout, a disease described in humans for at least 1000 years. Many lower organisms, such as the yeast Arxula adeninivorans, possess the enzyme, urate oxidase that converts uric acid to 5-hydroxyisourate, thus preventing uric acid accumulation. We have examined the complete purine degradation pathway in A. adeninivorans and analyzed enzymes involved. Recombinant adenine deaminase, guanine deaminase, urate oxidase and endogenous xanthine oxidoreductase have been investigated as potential additives to degrade purines in the food. Here, we review the current model of the purine degradation pathway of A. adeninivorans and present an overview of proposed enzyme system with perspectives for its further development.
人类体内的嘌呤降解途径以尿酸为终点,尿酸的水溶性较低。当嘌呤摄入量增加或肾功能受损导致尿酸生成增加时,尿酸会在血液中积聚(高尿酸血症)。这会增加痛风的风险,痛风这种疾病在人类中已有至少1000年的记载。许多低等生物,如酵母嗜腺嘌呤阿苏菌,拥有尿酸氧化酶,该酶可将尿酸转化为5-羟基异尿酸,从而防止尿酸积累。我们研究了嗜腺嘌呤阿苏菌完整的嘌呤降解途径,并分析了其中涉及的酶。重组腺嘌呤脱氨酶、鸟嘌呤脱氨酶、尿酸氧化酶和内源性黄嘌呤氧化还原酶已作为降解食物中嘌呤的潜在添加剂进行了研究。在此,我们综述了嗜腺嘌呤阿苏菌嘌呤降解途径的当前模型,并概述了所提出的酶系统及其进一步发展的前景。