Echavarri-Erasun Carlos, Johnson Eric A
Department of Food Microbiology and Toxicology, University of Wisconsin-Madison, Madison, WI 53706, USA.
FEMS Yeast Res. 2004 Jan;4(4-5):511-9. doi: 10.1016/S1567-1356(03)00177-6.
A fungal contaminant on an agar plate containing colonies of Xanthophyllomyces dendrorhous markedly increased carotenoid production by yeast colonies near to the fungal growth. Spent-culture filtrate from growth of the fungus in yeast-malt medium also stimulated carotenoid production by X. dendrorhous. Four X. dendrorhous strains including the wild-type UCD 67-385 (ATCC 24230), AF-1 (albino mutant, ATCC 96816), Yan-1 (beta-carotene mutant, ATCC 96815) and CAX (astaxanthin overproducer mutant) exposed to fungal concentrate extract enhanced astaxanthin up to approximately 40% per unit dry cell weight in the wild-type strain and in CAX. Interestingly, the fungal extract restored astaxanthin biosynthesis in non-astaxanthin-producing mutants previously isolated in our laboratory, including the albino and the beta-carotene mutant. The fungus was identified as Epicoccum nigrum by morphology of sporulating cultures, and the identity confirmed by genetic characterization including rDNA sequencing analysis of the large-subunit (LSU), the internal transcribed spacer, and the D1/D2 region of the LSU. These E. nigrum rDNA sequences were deposited in GenBank under accesssion numbers AF338443, AY093413 and AY093414. Systematic rDNA homology alignments were performed to identify fungi related to E. nigrum. Stimulation of carotenogenesis by E. nigrum and potentially other fungi could provide a novel method to enhance astaxanthin formation in industrial fermentations of X. dendrorhous and Phaffia rhodozyma.
在含有红酵母菌落的琼脂平板上,一种真菌污染物显著增加了靠近真菌生长处的酵母菌落的类胡萝卜素产量。真菌在酵母 - 麦芽培养基中生长的发酵液滤液也刺激了红酵母的类胡萝卜素产量。包括野生型UCD 67 - 385(ATCC 24230)、AF - 1(白化突变体,ATCC 96816)、Yan - 1(β - 胡萝卜素突变体,ATCC 96815)和CAX(虾青素高产突变体)在内的四株红酵母菌株,暴露于真菌浓缩提取物后,野生型菌株和CAX中虾青素产量每单位干细胞重量提高了约40%。有趣的是,真菌提取物恢复了我们实验室之前分离出的非虾青素产生突变体(包括白化突变体和β - 胡萝卜素突变体)中的虾青素生物合成。通过产孢培养物的形态学鉴定该真菌为黑附球菌,并通过包括大亚基(LSU)的rDNA测序分析、内部转录间隔区以及LSU的D1/D2区域的遗传特征分析来确认其身份。这些黑附球菌的rDNA序列已以登录号AF338443、AY093413和AY093414保存在GenBank中。进行了系统的rDNA同源性比对以鉴定与黑附球菌相关的真菌。黑附球菌以及可能的其他真菌对类胡萝卜素生成的刺激作用,可为在红酵母和红发夫酵母的工业发酵中提高虾青素形成提供一种新方法