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      Light regulates chlorophyll biosynthesis via ELIP1 during the storage of Chinese cabbage

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          Abstract

          Chlorophyll loss is a major problem during green vegetable storage. However, the molecular mechanism is still unclear. In this study, a 21 days of storage experiments showed chlorophyll content was higher in light-stored Chinese cabbage ( Brassica chinensis L .) leaves than those in dark-stored samples. Transcriptome analyses were performed on these samples to determine the effects of light. Among 311 differentially expressed genes (DEGs), early light-induced protein 1 (ELIP1) was identified as the main control gene for chlorophyll synthesis. Tissues and subcellular localization indicated that ELIP1 was localized in the nucleus. Motifs structure analyses, chromatin immunoprecipitation (ChIP) assays, luciferase reporter assays, and overexpression experiments demonstrated that ELIP1 regulated the expressions of genomes uncoupled 4 ( GUN4), Glutamyl-tRNA reductase family protein ( HEMA1), and Mg-protoporphyrin IX methyltransferase (CHLM) by binding to G-box-like motifs and affected chlorophyll biosynthesis during the storage of Chinese cabbage. It is a possible common tetrapyrrole biosynthetic pathway for chlorophylls, hemes, and bilin pigments in photosynthetic organisms. Our research also revealed that white light can be used as a regulatory factor to improve the storage ability and extent shelf life of Chinese cabbage.

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          Chlorophyll degradation during senescence.

          The catabolic pathway of chlorophyll (Chl) during senescence and fruit ripening leads to the accumulation of colorless breakdown products (NCCs). This review updates an earlier review on Chl breakdown published here in 1999 ( 69 ). It summarizes recent advances in the biochemical reactions of the pathway and describes the characterization of new NCCs and their formation inside the vacuole. Furthermore, I focus on the recent molecular identification of three chl catabolic enzymes, chlorophyllase, pheophorbide a oxygenase (PAO), and red Chl catabolite reductase (RCCR). The analysis of Chl catabolic mutants demonstrates the importance of Chl breakdown for plant development and survival. Mutants defective in PAO or RCCR develop a lesion mimic phenotype, due to the accumulation of breakdown intermediates. Thus, Chl breakdown is a prerequisite to detoxify the potentially phototoxic pigment within the vacuoles in order to permit the remobilization of nitrogen from Chl-binding proteins to proceed during senescence.
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            The light-harvesting chlorophyll a/b binding proteins Lhcb1 and Lhcb2 play complementary roles during state transitions in Arabidopsis.

            Photosynthetic light harvesting in plants is regulated by phosphorylation-driven state transitions: functional redistributions of the major trimeric light-harvesting complex II (LHCII) to balance the relative excitation of photosystem I and photosystem II. State transitions are driven by reversible LHCII phosphorylation by the STN7 kinase and PPH1/TAP38 phosphatase. LHCII trimers are composed of Lhcb1, Lhcb2, and Lhcb3 proteins in various trimeric configurations. Here, we show that despite their nearly identical amino acid composition, the functional roles of Lhcb1 and Lhcb2 are different but complementary. Arabidopsis thaliana plants lacking only Lhcb2 contain thylakoid protein complexes similar to wild-type plants, where Lhcb2 has been replaced by Lhcb1. However, these do not perform state transitions, so phosphorylation of Lhcb2 seems to be a critical step. In contrast, plants lacking Lhcb1 had a more profound antenna remodeling due to a decrease in the amount of LHCII trimers influencing thylakoid membrane structure and, more indirectly, state transitions. Although state transitions are also found in green algae, the detailed architecture of the extant seed plant light-harvesting antenna can now be dated back to a time after the divergence of the bryophyte and spermatophyte lineages, but before the split of the angiosperm and gymnosperm lineages more than 300 million years ago. © 2014 American Society of Plant Biologists. All rights reserved.
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              Multigene manipulation of photosynthetic carbon assimilation increases CO2 fixation and biomass yield in tobacco

              Highlight Multigene manipulation of levels of Calvin cycle enzymes, together with the introduction of a putative cyanobacterial inorganic carbon transporter, results in substantial improvements in biomass yield. This study demonstrates that this approach has the potential to produce crop plants to meet the food requirements of a growing population.
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                Author and article information

                Contributors
                wangtuoyi@hotmail.com
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                30 June 2022
                30 June 2022
                2022
                : 12
                : 11098
                Affiliations
                [1 ]GRID grid.412616.6, ISNI 0000 0001 0002 2355, College of Food and Biological Engineering, , Qiqihar University, ; Qiqihar, 161006 China
                [2 ]GRID grid.412616.6, ISNI 0000 0001 0002 2355, College of Life Sciences, Agriculture and Forestry, , Qiqihar University, ; Qiqihar, 161006 China
                Article
                15451
                10.1038/s41598-022-15451-9
                9247097
                35773334
                6cd562ba-7222-4ac8-8558-f2b3c327d6b6
                © The Author(s) 2022

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 21 February 2022
                : 23 June 2022
                Funding
                Funded by: Natural Science Foundation of Heilongjiang Province (LC2019C066)
                Award ID: LC2019C066
                Award Recipient :
                Funded by: special fund for plant food processing technology from the Colleges and Universities Basic Scientific Research Project in Heilongjiang Province
                Award ID: YSTSXK201829
                Award ID: YSTSXK201876
                Award ID: YSTSXK201812
                Funded by: Fundamental Research Funds of Department of Education of Heilongjiang Province
                Award ID: 135209371
                Award ID: 135309371
                Funded by: Qiqihar University Graduate Innovative Research Project
                Award ID: YJSCX2019079
                Categories
                Article
                Custom metadata
                © The Author(s) 2022

                Uncategorized
                plant sciences,light responses,plant molecular biology,plant stress responses
                Uncategorized
                plant sciences, light responses, plant molecular biology, plant stress responses

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