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Correlation between lipid and carotenoid synthesis in torularhodin-producing Rhodotorula glutinis

机译:产环状小红球菌Rhodotorula glutinis中脂质与类胡萝卜素合成的相关性

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The oleaginous red yeast Rhodotorula glutinis produces carotenoid pigments, especially torularhodin and β-carotene, in significant amounts. We have analyzed in detail carotenoid and lipid biosynthesis in a torularhodin-producing strain of R. glutinis cultivated at different carbon:nitrogen (C/N) ratios (20:1, 50:1, 70:1, and 100:1). When the strain was cultivated in media with low C/N ratios (20:1 and 50:1), glucose was completely utilized and carotenoid formation was stimulated. Maximum pigment production reached 12.9?mg/L of medium and 2.3?mg/g of biomass at the C/N ratio of 20:1. It was noted that β-carotene synthesis was prominent when glucose was present in the medium. However, glucose exhaustion in the media at C/N ratios of 20:1 and 50:1 was closely accompanied by the predominant formation of torularhodin. The growth of R. glutinis in media with C/N ratios of 70:1 and 100:1 favored lipid accumulation in the cells but carotenoid biosynthesis was reduced. In addition, glucose consumption was linked to a rapid decrease in oleic acid levels in the total intracellular lipids. The kinetic analysis clearly indicated a correlation between oleic acid levels in total lipids and torularhodin accumulation in the cells. The results may suggest that acetyl-CoA formed from oleic acid degradation is metabolized through the mevalonate/isoprenoid/carotenoid pathways directly to torularhodin.
机译:含油的红色酵母Rhodotorula glutinis产生大量的类胡萝卜素色素,特别是类固醇和β-胡萝卜素。我们已经详细分析了在以不同碳:氮(C / N)比(20:1、50:1、70:1和100:1)培养的R. glutinis产类固醇的菌株中类胡萝卜素和脂质的生物合成。当在低C / N比(20:1和50:1)的培养基中培养菌株时,葡萄糖被完全利用,并刺激了类胡萝卜素的形成。 C / N比为20:1时,最大的色素产量达到12.9?mg / L的培养基和2.3?mg / g的生物质。注意到当培养基中存在葡萄糖时,β-胡萝卜素合成突出。然而,C / N比为20:1和50:1的培养基中葡萄糖的消耗与主要形成的torularhodin密切相关。 C / N比为70:1和100:1的培养基中,R.glutinis的生长有利于脂质在细胞中的积累,但类胡萝卜素的生物合成却减少了。此外,葡萄糖的消耗与总细胞内脂质中油酸水平的快速下降有关。动力学分析清楚地表明,总脂质中的油酸水平与细胞中的类固醇积累之间存在相关性。结果可能表明,由油酸降解形成的乙酰辅酶A通过甲羟戊酸/异戊二烯/类胡萝卜素途径代谢成环戊丁。

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