Targeted Mutations Produce Divergent Characteristics in Pedigreed Sake Yeast Strains
Modification of the genetic background and, in some cases, the introduction of targeted mutations can play a critical role in producing trait characteristics during the breeding of crops, livestock, and microorganisms. However, the question of how similar trait characteristics emerge when the same t...
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Published in | Microorganisms (Basel) Vol. 11; no. 5; p. 1274 |
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Main Authors | , , , , , , , , , , , , , |
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Abstract | Modification of the genetic background and, in some cases, the introduction of targeted mutations can play a critical role in producing trait characteristics during the breeding of crops, livestock, and microorganisms. However, the question of how similar trait characteristics emerge when the same target mutation is introduced into different genetic backgrounds is unclear. In a previous study, we performed genome editing of
,
,
, and
on the standard sake yeast strain Kyokai No. 7 to breed a sake yeast with multiple excellent brewing characteristics. By introducing the same targeted mutations into other pedigreed sake yeast strains, such as Kyokai strains No. 6, No. 9, and No. 10, we were able to create sake yeasts with the same excellent brewing characteristics. However, we found that other components of sake made by the genome-edited yeast strains did not change in the exact same way. For example, amino acid and isobutanol contents differed among the strain backgrounds. We also showed that changes in yeast cell morphology induced by the targeted mutations also differed depending on the strain backgrounds. The number of commonly changed morphological parameters was limited. Thus, divergent characteristics were produced by the targeted mutations in pedigreed sake yeast strains, suggesting a breeding strategy to generate a variety of sake yeasts with excellent brewing characteristics. |
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AbstractList | Modification of the genetic background and, in some cases, the introduction of targeted mutations can play a critical role in producing trait characteristics during the breeding of crops, livestock, and microorganisms. However, the question of how similar trait characteristics emerge when the same target mutation is introduced into different genetic backgrounds is unclear. In a previous study, we performed genome editing of AWA1, CAR1, MDE1, and FAS2 on the standard sake yeast strain Kyokai No. 7 to breed a sake yeast with multiple excellent brewing characteristics. By introducing the same targeted mutations into other pedigreed sake yeast strains, such as Kyokai strains No. 6, No. 9, and No. 10, we were able to create sake yeasts with the same excellent brewing characteristics. However, we found that other components of sake made by the genome-edited yeast strains did not change in the exact same way. For example, amino acid and isobutanol contents differed among the strain backgrounds. We also showed that changes in yeast cell morphology induced by the targeted mutations also differed depending on the strain backgrounds. The number of commonly changed morphological parameters was limited. Thus, divergent characteristics were produced by the targeted mutations in pedigreed sake yeast strains, suggesting a breeding strategy to generate a variety of sake yeasts with excellent brewing characteristics. Modification of the genetic background and, in some cases, the introduction of targeted mutations can play a critical role in producing trait characteristics during the breeding of crops, livestock, and microorganisms. However, the question of how similar trait characteristics emerge when the same target mutation is introduced into different genetic backgrounds is unclear. In a previous study, we performed genome editing of AWA1 , CAR1 , MDE1 , and FAS2 on the standard sake yeast strain Kyokai No. 7 to breed a sake yeast with multiple excellent brewing characteristics. By introducing the same targeted mutations into other pedigreed sake yeast strains, such as Kyokai strains No. 6, No. 9, and No. 10, we were able to create sake yeasts with the same excellent brewing characteristics. However, we found that other components of sake made by the genome-edited yeast strains did not change in the exact same way. For example, amino acid and isobutanol contents differed among the strain backgrounds. We also showed that changes in yeast cell morphology induced by the targeted mutations also differed depending on the strain backgrounds. The number of commonly changed morphological parameters was limited. Thus, divergent characteristics were produced by the targeted mutations in pedigreed sake yeast strains, suggesting a breeding strategy to generate a variety of sake yeasts with excellent brewing characteristics. Modification of the genetic background and, in some cases, the introduction of targeted mutations can play a critical role in producing trait characteristics during the breeding of crops, livestock, and microorganisms. However, the question of how similar trait characteristics emerge when the same target mutation is introduced into different genetic backgrounds is unclear. In a previous study, we performed genome editing of , , , and on the standard sake yeast strain Kyokai No. 7 to breed a sake yeast with multiple excellent brewing characteristics. By introducing the same targeted mutations into other pedigreed sake yeast strains, such as Kyokai strains No. 6, No. 9, and No. 10, we were able to create sake yeasts with the same excellent brewing characteristics. However, we found that other components of sake made by the genome-edited yeast strains did not change in the exact same way. For example, amino acid and isobutanol contents differed among the strain backgrounds. We also showed that changes in yeast cell morphology induced by the targeted mutations also differed depending on the strain backgrounds. The number of commonly changed morphological parameters was limited. Thus, divergent characteristics were produced by the targeted mutations in pedigreed sake yeast strains, suggesting a breeding strategy to generate a variety of sake yeasts with excellent brewing characteristics. |
Audience | Academic |
Author | Ohnuki, Shinsuke Nishida, Ikuhisa Hirata, Dai Kitamoto, Katsuhiko Ohya, Yoshikazu Goshima, Tetsuya Akao, Takeshi Tomiyama, Saki Chadani, Tomoya Ghanegolmohammadi, Farzan Nishi, Tomoyuki Klinkaewboonwong, Norapat Ushiyama, Yuto Isogai, Atsuko |
AuthorAffiliation | 4 National Research Institute of Brewing, Higashi-Hiroshima, Hiroshima 739-0046, Japan; isogai@nrib.go.jp (A.I.); t.goshima@nrib.go.jp (T.G.); akao_t@nrib.go.jp (T.A.) 5 Program of Biotechnology, Graduate School of Integrated Sciences for Life, Hiroshima University, 1-3-1 Kagamiyama, Higashi-Hiroshima 739-8530, Japan 9 Collaborative Research Institute for Innovative Microbiology, The University of Tokyo, Tokyo 113-8657, Japan 2 Sakeology Center, Niigata University, 2-8050, Ikarashi, Niigata 950-2181, Japan; i-nishida@sake.nu.niigata-u.ac.jp 7 Sake Research Center, Asahi Sake Brewing Co., Ltd., Nagaoka, Niigata 949-5494, Japan; nishitomoyuki@asahi-shuzo.co.jp 3 Sakeology Course, Graduate School of Science and Technology, Niigata University, 2-8050, Ikarashi, Niigata 950-2181, Japan; f22d057j@mail.cc.niigata-u.ac.jp (Y.U.); f22d060j@mail.cc.niigata-u.ac.jp (S.T.) 8 Department of Pharmaceutical and Medical Business Sciences, Nihon Pharmaceutical University, Bunkyo-ku, Tokyo 113-0034, Japan; k-k |
AuthorAffiliation_xml | – name: 5 Program of Biotechnology, Graduate School of Integrated Sciences for Life, Hiroshima University, 1-3-1 Kagamiyama, Higashi-Hiroshima 739-8530, Japan – name: 1 Department of Integrated Biosciences, Graduate School of Frontier Sciences, The University of Tokyo, Chiba 277-8562, Japan; 8124564286@edu.k.u-tokyo.ac.jp (N.K.); ohnuki@edu.k.u-tokyo.ac.jp (S.O.); tc.biology0048@gmail.com (T.C.); farzang@mit.edu (F.G.) – name: 8 Department of Pharmaceutical and Medical Business Sciences, Nihon Pharmaceutical University, Bunkyo-ku, Tokyo 113-0034, Japan; k-kitamoto@nichiyaku.ac.jp – name: 3 Sakeology Course, Graduate School of Science and Technology, Niigata University, 2-8050, Ikarashi, Niigata 950-2181, Japan; f22d057j@mail.cc.niigata-u.ac.jp (Y.U.); f22d060j@mail.cc.niigata-u.ac.jp (S.T.) – name: 4 National Research Institute of Brewing, Higashi-Hiroshima, Hiroshima 739-0046, Japan; isogai@nrib.go.jp (A.I.); t.goshima@nrib.go.jp (T.G.); akao_t@nrib.go.jp (T.A.) – name: 6 Department of Biological Engineering, Massachusetts Institute of Technology, Cambridge, MA 02139, USA – name: 7 Sake Research Center, Asahi Sake Brewing Co., Ltd., Nagaoka, Niigata 949-5494, Japan; nishitomoyuki@asahi-shuzo.co.jp – name: 2 Sakeology Center, Niigata University, 2-8050, Ikarashi, Niigata 950-2181, Japan; i-nishida@sake.nu.niigata-u.ac.jp – name: 9 Collaborative Research Institute for Innovative Microbiology, The University of Tokyo, Tokyo 113-8657, Japan |
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CitedBy_id | crossref_primary_10_1093_bbb_zbad167 crossref_primary_10_1093_bbb_zbae003 crossref_primary_10_1093_femsyr_foad056 crossref_primary_10_1016_j_mimet_2023_106840 |
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Keywords | genome editing FAS2 CRISPR/Cas9 sake yeast Saccharomyces cerevisiae |
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SubjectTerms | Alcohol Amino acids Breweries Brewing Cell morphology Chromatography CRISPR/Cas9 Cytology Ethanol FAS2 Fermentation Genetic aspects Genetic testing Genome editing Genomes Genomics Glucose Isobutanol Livestock Microorganisms Morphology Mutation Plant breeding Production processes Proteins Rice wines Saccharomyces cerevisiae sake yeast Software Strains (organisms) Yeast Yeast fungi Yeasts |
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Title | Targeted Mutations Produce Divergent Characteristics in Pedigreed Sake Yeast Strains |
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