Department of Biotechnology and Bioengineering, Cinvestav-IPN, Av. Instituto Politécnico Nacional 2508, Col. San Pedro Zacatenco, 07360, Mexico City, Mexico.
College of Science and Technology Studies of the State of Michoacán, Loma de las Liebres 180, Fraccionamiento Lomas del Sur, 58095, Morelia, Michoacán, Mexico.
Microb Cell Fact. 2018 Apr 3;17(1):53. doi: 10.1186/s12934-018-0898-7.
Growth conditions that bring about stress on Phaffia rhodozyma cells encourage the synthesis of astaxanthin, an antioxidant carotenoid, which protects cells against oxidative damage. Using P. rhodozyma cultures performed with and without copper limitation, we examined the kinetics of astaxanthin synthesis along with the expression of asy, the key astaxanthin synthesis gene, as well as aox, which encodes an alternative oxidase protein.
Copper deficiency had a detrimental effect on the rates of oxygen consumption and ethanol reassimilation at the diauxic shift. In contrast, copper deficiency prompted alcoholic fermentation under aerobic conditions and had a favorable effect on the astaxanthin content of cells, as well as on aox expression. Both cultures exhibited strong aox expression while consuming ethanol, but particularly when copper was absent.
We show that the induction of either astaxanthin production, aox expression, or aerobic fermentation exemplifies the crucial role that redox imbalance plays in triggering any of these phenomena. Based on our own results and data from others, we propose a mechanism that rationalizes the central role played by changes of respiratory activity, which lead to redox imbalances, in triggering both the short-term antioxidant response as well as fermentation in yeasts and other cell types.
使 Phaffia rhodozyma 细胞产生应激的生长条件会促进抗氧化类胡萝卜素虾青素的合成,虾青素可以保护细胞免受氧化损伤。我们使用有和没有铜限制的 P. rhodozyma 培养物,研究了虾青素合成的动力学以及关键虾青素合成基因 asy 和编码替代氧化酶蛋白的 aox 的表达。
铜缺乏对酒精发酵过程中两次生长转换时的耗氧率和乙醇再吸收率有不利影响。相比之下,铜缺乏会促使有氧条件下的酒精发酵,并对细胞虾青素含量和 aox 表达产生有利影响。两种培养物在消耗乙醇时都表现出强烈的 aox 表达,但在铜缺乏时更为明显。
我们表明,虾青素的诱导产生、aox 的表达或有氧发酵都表明了氧化还原失衡在触发这些现象中的关键作用。基于我们自己的结果和其他人的数据,我们提出了一个机制,该机制合理化了呼吸活性变化在触发酵母和其他细胞类型的短期抗氧化反应和发酵中的核心作用,这些变化导致了氧化还原失衡。