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Overexpression of BUNDLE SHEATH DEFECTIVE 2 improves the efficiency of photosynthesis and growth in Arabidopsis.
Busch, Florian A; Tominaga, Jun; Muroya, Masato; Shirakami, Norihiko; Takahashi, Shunichi; Yamori, Wataru; Kitaoka, Takuya; Milward, Sara E; Nishimura, Kohji; Matsunami, Erika; Toda, Yosuke; Higuchi, Chikako; Muranaka, Atsuko; Takami, Tsuneaki; Watanabe, Shunsuke; Kinoshita, Toshinori; Sakamoto, Wataru; Sakamoto, Atsushi; Shimada, Hiroshi.
Affiliation
  • Busch FA; Research School of Biology, Australian National University, Canberra, Australian Capital Territory, 2601, Australia.
  • Tominaga J; Graduate School of Integrated Sciences for Life, Hiroshima University, 1-3-1 Kagamiyama, Higashi-Hiroshima, 739-8526, Japan.
  • Muroya M; Graduate School of Integrated Sciences for Life, Hiroshima University, 1-3-1 Kagamiyama, Higashi-Hiroshima, 739-8526, Japan.
  • Shirakami N; Graduate School of Integrated Sciences for Life, Hiroshima University, 1-3-1 Kagamiyama, Higashi-Hiroshima, 739-8526, Japan.
  • Takahashi S; Research School of Biology, Australian National University, Canberra, Australian Capital Territory, 2601, Australia.
  • Yamori W; Graduate School of Science, University of Tokyo, Bunkyo-ku, Tokyo, 113-0033, Japan.
  • Kitaoka T; Division of Biological Science, Graduate School of Science, Nagoya University, Chikusa, Nagoya, 464-8602, Japan.
  • Milward SE; Research School of Biology, Australian National University, Canberra, Australian Capital Territory, 2601, Australia.
  • Nishimura K; Department of Molecular and Functional Genomics, Interdisciplinary Center for Science Research, Organization of Research, Shimane University, Nishikawatsu 1060, Matsue, 690-8504, Japan.
  • Matsunami E; Department of Molecular and Functional Genomics, Interdisciplinary Center for Science Research, Organization of Research, Shimane University, Nishikawatsu 1060, Matsue, 690-8504, Japan.
  • Toda Y; Graduate School of Science, University of Tokyo, Bunkyo-ku, Tokyo, 113-0033, Japan.
  • Higuchi C; Graduate School of Integrated Sciences for Life, Hiroshima University, 1-3-1 Kagamiyama, Higashi-Hiroshima, 739-8526, Japan.
  • Muranaka A; Graduate School of Integrated Sciences for Life, Hiroshima University, 1-3-1 Kagamiyama, Higashi-Hiroshima, 739-8526, Japan.
  • Takami T; Institute of Plant Science and Resources, Okayama University, Kurashiki, Okayama, 710-0046, Japan.
  • Watanabe S; Graduate School of Integrated Sciences for Life, Hiroshima University, 1-3-1 Kagamiyama, Higashi-Hiroshima, 739-8526, Japan.
  • Kinoshita T; Division of Biological Science, Graduate School of Science, Nagoya University, Chikusa, Nagoya, 464-8602, Japan.
  • Sakamoto W; Institute of Transformative Bio-Molecules (WPI-ITbM), Nagoya University, Chikusa, Nagoya, 464-8602, Japan.
  • Sakamoto A; Institute of Plant Science and Resources, Okayama University, Kurashiki, Okayama, 710-0046, Japan.
  • Shimada H; Graduate School of Integrated Sciences for Life, Hiroshima University, 1-3-1 Kagamiyama, Higashi-Hiroshima, 739-8526, Japan.
Plant J ; 102(1): 129-137, 2020 04.
Article in En | MEDLINE | ID: mdl-31755157
Bundle Sheath Defective 2, BSD2, is a stroma-targeted protein initially identified as a factor required for the biogenesis of ribulose 1,5-bisphosphate carboxylase/oxygenase (RuBisCO) in maize. Plants and algae universally have a homologous gene for BSD2 and its deficiency causes a RuBisCO-less phenotype. As RuBisCO can be the rate-limiting step in CO2 assimilation, the overexpression of BSD2 might improve photosynthesis and productivity through the accumulation of RuBisCO. To examine this hypothesis, we produced BSD2 overexpression lines in Arabidopsis. Compared with wild type, the BSD2 overexpression lines BSD2ox-2 and BSD2ox-3 expressed 4.8-fold and 8.8-fold higher BSD2 mRNA, respectively, whereas the empty-vector (EV) harbouring plants had a comparable expression level. The overexpression lines showed a significantly higher CO2 assimilation rate per available CO2 and productivity than EV plants. The maximum carboxylation rate per total catalytic site was accelerated in the overexpression lines, while the number of total catalytic sites and RuBisCO content were unaffected. We then isolated recombinant BSD2 (rBSD2) from E. coli and found that rBSD2 reduces disulfide bonds using reductants present in vivo, for example glutathione, and that rBSD2 has the ability to reactivate RuBisCO that has been inactivated by oxidants. Furthermore, 15% of RuBisCO freshly isolated from leaves of EV was oxidatively inactivated, as compared with 0% in BSD2-overexpression lines, suggesting that the overexpression of BSD2 maintains RuBisCO to be in the reduced active form in vivo. Our results demonstrated that the overexpression of BSD2 improves photosynthetic efficiency in Arabidopsis and we conclude that it is involved in mediating RuBisCO activation.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Photosynthesis / Arabidopsis / Arabidopsis Proteins Type of study: Prognostic_studies Language: En Journal: Plant J Journal subject: BIOLOGIA MOLECULAR / BOTANICA Year: 2020 Document type: Article Affiliation country: Australia Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Photosynthesis / Arabidopsis / Arabidopsis Proteins Type of study: Prognostic_studies Language: En Journal: Plant J Journal subject: BIOLOGIA MOLECULAR / BOTANICA Year: 2020 Document type: Article Affiliation country: Australia Country of publication: United kingdom