Selection of the methylotrophic yeast Ogataea minuta as a high-producing host for heterologous protein expression

被引:2
|
作者
Tsuda, Masashi [1 ]
Nakatani, Yuki [1 ]
Baba, Satoshi [1 ]
Tanaka, Isshin [2 ]
Ichikawa, Kimihisa [1 ]
Nonaka, Koichi [1 ]
Ito, Rie [3 ]
Yoko-o, Takehiko [3 ]
Chiba, Yasunori [3 ]
机构
[1] Daiichi Sankyo Co Ltd, Biol Technol Res Labs, 2716-1 Kurakake, Tokyo, Gunma 3700503, Japan
[2] Daiichi Sankyo RD Novare Co Ltd, Organ Synth Dept, Nat Prod Res Grp, 1-16-13 Kitakasai,Edogawa ku, Tokyo 1348630, Japan
[3] Natl Inst Adv Ind Sci & Technol, Cellular & Mol Biotechnol Res Inst, 1-1-1 Higashi, Tsukuba, Ibaraki 3058565, Japan
关键词
Protein expression; Methylotrophic yeast; Ogataea; Taxonomy; Monocolony isolation; EFFICIENT ANTIBODY-PRODUCTION; TRANSCRIPTION-FACTOR; METHANOL; HANSENULA; GENE; DNA; IDENTIFICATION; ACTIVATION; PROMOTER; REPORTER;
D O I
10.1016/j.jbiosc.2022.12.006
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
January 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 nocti-luca 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 under -standing 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.(c) 2022, The Society for Biotechnology, Japan. All rights reserved.
引用
收藏
页码:196 / 202
页数:7
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