Suparmin Ahmad, Kato Tatsuya, Dohra Hideo, Park Enoch Y
Laboratory of Biotechnology, Department of Agriculture, Graduate School of Integrated Science and Technology, Shizuoka University, Ohya, Suruga-ku, Shizuoka, Japan.
Laboratory of Biotechnology, Green Chemistry Research Division, Research Institute of Green Science and Technology, Shizuoka University, Ohya, Suruga-ku, Shizuoka, Japan.
PLoS One. 2017 Nov 1;12(11):e0187052. doi: 10.1371/journal.pone.0187052. eCollection 2017.
Cordyceps militaris produces cordycepin, which is known to be a bioactive compound. Currently, cordycepin hyperproduction of C. militaris was carried out in a liquid surface culture because of its low productivity in a submerged culture, however the reason was not known. In this study, 4.92 g/L of cordycepin was produced at the 15th day of C. militaris NBRC 103752 liquid surface culture, but only 1 mg/L was produced in the submerged culture. RNA-Seq was used to clarify the gene expression profiles of the cordycepin biosynthetic pathways of the submerged culture and the liquid surface culture. From this analysis, 1036 genes were shown to be upregulated and 557 genes were downregulated in the liquid surface culture compared with the submerged culture. Specifically, adenylosuccinate synthetase and phosphoribosylaminoimidazole-succinocarboxamide (SAICAR) synthase in purine nucleotide metabolism were significantly upregulated in the liquid surface culture. Thick mycelia formation in the liquid surface culture was found to induce the expression of hypoxia-related genes (GABA shunt, glutamate synthetase precursor, and succinate-semialdehyde dehydrogenase). Cytochrome P450 oxidoreductases containing heme were also found to be significantly enriched, suggesting that a hypoxic condition might be created in the liquid surface culture. These results suggest that hypoxic conditions are more suitable for cordycepin production in the liquid surface culture compared with the submerged culture. Our analysis paves the way for unraveling the cordycepin biosynthesis pathway and for improving cordycepin production in C. militaris.
北虫草可产生虫草素,这是一种已知的生物活性化合物。目前,由于北虫草在深层培养中的产量较低,其虫草素的过量生产是在液体表面培养中进行的,但其原因尚不清楚。在本研究中,北虫草NBRC 103752液体表面培养第15天产生了4.92 g/L的虫草素,但在深层培养中仅产生了1 mg/L。RNA测序用于阐明深层培养和液体表面培养中虫草素生物合成途径的基因表达谱。通过该分析,与深层培养相比,液体表面培养中有1036个基因上调,557个基因下调。具体而言,嘌呤核苷酸代谢中的腺苷酸琥珀酸合成酶和磷酸核糖氨基咪唑-琥珀酰胺羧酰胺(SAICAR)合成酶在液体表面培养中显著上调。发现液体表面培养中厚菌丝体的形成会诱导缺氧相关基因(GABA分流、谷氨酸合成酶前体和琥珀酸半醛脱氢酶)的表达。还发现含血红素的细胞色素P450氧化还原酶显著富集,表明液体表面培养中可能产生了缺氧条件。这些结果表明,与深层培养相比,缺氧条件更适合液体表面培养中虫草素的生产。我们的分析为揭示虫草素生物合成途径和提高北虫草中虫草素的产量铺平了道路。