Biologics Technology Research Laboratories, Daiichi Sankyo Co., Ltd., 2716-1 Kurakake, Akaiwa, Chiyoda, Gunma 370-0503, Japan.
Biologics Technology Research Laboratories, Daiichi Sankyo Co., Ltd., 2716-1 Kurakake, Akaiwa, Chiyoda, Gunma 370-0503, Japan.
J Biosci Bioeng. 2023 Mar;135(3):196-202. doi: 10.1016/j.jbiosc.2022.12.006. Epub 2023 Jan 24.
Three Ogataea minuta var. minuta strains have been deposited as NBRC 0975, NBRC 10402, and NBRC 10746 in the National Institute of Technology and Evaluation (NITE) Biological Resource Center (NBRC) collection. We investigated the ability to produce secretory proteins and several genotypic and phenotypic characteristics in order to select the best strain for heterologous protein expression. NBRC 10746 showed the best performance as evaluated by Cypridina noctiluca luciferase expression. Subsequently, clone #5-30 named tat06213, which was obtained by single-colony isolation from NBRC 10746, was established as a promising host for heterologous protein expression. To deepen our understanding of the characteristics of O.minuta var. minuta strains, sequence analysis of the D1/D2 domain of large subunit rRNA was conducted and the resulting phylogenetic tree derived from the D1/D2 domain showed that NBRC 10402 and NBRC 10746 were grouped into a different cluster far from NBRC 0975. Furthermore, a chromosome structure topology with electrophoretic karyotype and AOX1 loci analyzed by pulsed-field gel electrophoresis with Southern blotting showed different chromosome patterns and AOX1-hybridization loci among the strains. Additionally, the sequences of the promoter regions of the cloned AOX1 genes were not identical among the three strains. These findings might explain the differences in heterologous protein expression among the tested O. minuta var. minuta strains.
三株 Ogataea minuta var. minuta 菌株已被保藏于国立研究开发法人产业技术综合研究所生物资源中心(NBRC),编号分别为 NBRC 0975、NBRC 10402 和 NBRC 10746。为了筛选出最适合异源蛋白表达的菌株,我们对其产生分泌蛋白的能力和几种基因型及表型特征进行了研究。Cypridina noctiluca 荧光素酶表达结果表明,NBRC 10746 表现最佳。随后,从 NBRC 10746 中通过单菌落分离获得的克隆 #5-30 被命名为 tat06213,它被确立为异源蛋白表达的有前途的宿主。为了深入了解 O.minuta var. minuta 菌株的特性,我们对大亚基 rRNA 的 D1/D2 结构域进行了序列分析,基于 D1/D2 结构域构建的系统发育树表明,NBRC 10402 和 NBRC 10746 与 NBRC 0975 聚类不同,分属于不同的聚类。此外,通过脉冲场凝胶电泳结合 Southern 印迹技术对电泳核型和 AOX1 基因座进行分析,显示了不同菌株之间的染色体结构拓扑和 AOX1 杂交位点的差异。此外,三个菌株中克隆的 AOX1 基因启动子区域的序列并不完全相同。这些发现可能解释了测试的 O. minuta var. minuta 菌株之间异源蛋白表达的差异。