Molecular and Biological Function Research Core, Research Institute of Green Science and Technology, Shizuoka University, Ohya 836, Suruga-ku, Shizuoka, Japan.
Department of Agriculture, Graduate School of Integrated Science and Technology, Shizuoka University, Ohya 836, Suruga-ku, Shizuoka, Japan.
Mol Biotechnol. 2024 May;66(5):1144-1153. doi: 10.1007/s12033-023-01012-6. Epub 2024 Jan 7.
AgHST1 and AgHST3 genes encode sirtuins that are NAD-dependent protein deacetylases. According to previous reports, their disruption leads to the overproduction of riboflavin in Ashbya gossypii. In this study, we investigated the potential causes of riboflavin overproduction in the AgHST1Δ and AgHST3Δ mutant strains of A. gossypii. The generation of reactive oxygen species was increasd in the mutants compared to in WT. Additionally, membrane potential was lower in the mutants than in WT. The NAD/NADH ratio in AgHST1Δ mutant strain was lower than that in WT; however, the NAD/NADH ratio in AgHST3Δ was slightly higher than that in WT. AgHST1Δ mutant strain was more sensitive to high temperatures and hydroxyurea treatment than WT or AgHST3Δ. Expression of the AgGLR1 gene, encoding glutathione reductase, was substantially decreased in AgHST1Δ and AgHST3Δ mutant strains. The addition of N-acetyl-L-cysteine, an antioxidant, suppressed the riboflavin production in the mutants, indicating that it was induced by oxidative stress. Therefore, high oxidative stress resulting from the disruption of sirtuin genes induces riboflavin overproduction in AgHST1Δ and AgHST3Δ mutant strains. This study established that oxidative stress is an important trigger for riboflavin overproduction in sirtuin gene-disrupted mutant strains of A. gossypii and helped to elucidate the mechanism of riboflavin production in A. gossypii.
AgHST1 和 AgHST3 基因编码依赖 NAD 的蛋白去乙酰化酶 sirtuins。根据之前的报道,它们的缺失会导致棉铃象甲中核黄素的过量产生。在本研究中,我们研究了棉铃象甲 AgHST1Δ 和 AgHST3Δ 突变株中核黄素过量产生的潜在原因。与 WT 相比,突变体中活性氧的产生增加了。此外,与 WT 相比,突变体中的膜电位更低。AgHST1Δ 突变株中的 NAD/NADH 比值低于 WT;然而,AgHST3Δ 中的 NAD/NADH 比值略高于 WT。AgHST1Δ 突变株比 WT 或 AgHST3Δ 对高温和羟基脲处理更敏感。编码谷胱甘肽还原酶的 AgGLR1 基因在 AgHST1Δ 和 AgHST3Δ 突变株中的表达显著降低。抗氧化剂 N-乙酰-L-半胱氨酸的添加抑制了突变体中的核黄素产生,表明它是由氧化应激诱导的。因此,由于 sirtuin 基因的缺失导致的高氧化应激诱导了 AgHST1Δ 和 AgHST3Δ 突变株中核黄素的过量产生。本研究确立了氧化应激是 sirtuin 基因缺失突变株中核黄素过量产生的一个重要触发因素,并有助于阐明棉铃象甲中核黄素产生的机制。