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      Combined analysis of metagenome and transcriptome revealed the adaptive mechanism of different golden Camellia species in karst regions

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          Abstract

          Camellia sect. Chrysantha is an important rare and protected plant species. Some golden Camellia species grow in karst soil while others grow in acidic soil. In order to study the adaptation mechanism of golden Camellia to the karst environment, four species of golden Camellia growing in the karst soil ( Camellia pubipetala, Camellia perpetua, Camellia grandis, and Camellia limonia) and four species growing in the acidic soil ( Camellia nitidissima, Camellia euphlebia, Camellia tunghinensis, and Camellia parvipetala) were selected for this study. Combining the metagenome and transcriptome, the structure and function of the rhizosphere microbial communities and the gene expression in roots of golden Camellia were analyzed. The results showed that the rhizosphere microbial communities in different golden Camellia were significantly different in abundance of Acidobacteria, Actinobacteria, Candidatus_Rokubacteria, Nitrospirae, Planctomycetes, and Candidatus_Tectomicrobia. The proportion of Candidatus_Rokubacteria was significantly higher in the rhizosphere soil of four species of golden Camellia grown in karst areas, compared to C. nitidissima, C. euphlebia, and C. tunghinensis. The linear discriminant analysis Effect Size showed that C. parvipetala was similar to karst species in the enrichment of ABC transporters and quorum sensing. During the transcriptome analysis, numerous upregulated genes in four karst species, including CYP81E, CHS, F3H, C12RT1, NAS, and CAD, were found to be enriched in the secondary metabolite synthesis pathway in the KEGG library, when compared to C. tunghinensis. This study provides information for plant adaptation mechanisms on the rhizosphere soil microbial composition and gene expression in secondary metabolic pathways to karst habitats and its distribution in karst areas.

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          Most cited references46

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          Glycosyltransferases: structures, functions, and mechanisms.

          Glycosyltransferases catalyze glycosidic bond formation using sugar donors containing a nucleoside phosphate or a lipid phosphate leaving group. Only two structural folds, GT-A and GT-B, have been identified for the nucleotide sugar-dependent enzymes, but other folds are now appearing for the soluble domains of lipid phosphosugar-dependent glycosyl transferases. Structural and kinetic studies have provided new insights. Inverting glycosyltransferases utilize a direct displacement S(N)2-like mechanism involving an enzymatic base catalyst. Leaving group departure in GT-A fold enzymes is typically facilitated via a coordinated divalent cation, whereas GT-B fold enzymes instead use positively charged side chains and/or hydroxyls and helix dipoles. The mechanism of retaining glycosyltransferases is less clear. The expected two-step double-displacement mechanism is rendered less likely by the lack of conserved architecture in the region where a catalytic nucleophile would be expected. A mechanism involving a short-lived oxocarbenium ion intermediate now seems the most likely, with the leaving phosphate serving as the base.
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            FUNCTION AND MECHANISM OF ORGANIC ANION EXUDATION FROM PLANT ROOTS.

            The rhizosphere is the zone of soil immediately surrounding plant roots that is modified by root activity. In this critical zone, plants perceive and respond to their environment. As a consequence of normal growth and development, a large range of organic and inorganic substances are exchanged between the root and soil, which inevitably leads to changes in the biochemical and physical properties of the rhizosphere. Plants also modify their rhizosphere in response to certain environmental signals and stresses. Organic anions are commonly detected in this region, and their exudation from plant roots has now been associated with nutrient deficiencies and inorganic ion stresses. This review summarizes recent developments in the understanding of the function, mechanism, and regulation of organic anion exudation from roots. The benefits that plants derive from the presence of organic anions in the rhizosphere are described and the potential for biotechnology to increase organic anion exudation is highlighted.
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              How relevant are flavonoids as antioxidants in plants?

              Flavonoids are a large family of plant secondary metabolites, principally recognized for their health-promoting properties in human diets. Most flavonoids outperform well-known antioxidants, such as ascorbate (vitamin C) and alpha-tocopherol (vitamin E), in in vitro antioxidant assays because of their strong capacity to donate electrons or hydrogen atoms. However, experimental evidence for an antioxidant function in plants is limited to a few individual flavonoids under very specific experimental and developmental conditions. As we discuss here, although flavonoids have been demonstrated to accumulate with oxidative stress during abiotic and biotic environmental assaults, a convincing spatio-temporal correlation with the flavonoid oxidation products is not yet available. Thereby, the widely accepted antioxidant function of flavonoids in plants is still a matter of debate.
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                Author and article information

                Contributors
                Journal
                Front Plant Sci
                Front Plant Sci
                Front. Plant Sci.
                Frontiers in Plant Science
                Frontiers Media S.A.
                1664-462X
                20 November 2023
                2023
                : 14
                : 1180472
                Affiliations
                [1] 1 Guangxi Key Laboratory of Plant Functional Phytochemicals and Sustainable Utilization, Guangxi Institute of Botany, The Chinese Academy of Sciences , Guilin, China
                [2] 2 Key Laboratory of Ecology of Rare and Endangered Species and Environmental Protection, Guangxi Key Laboratory of Landscape Resources Conservation and Sustainable Utilization in Lijiang River Basin, College of Life Science, Guangxi Normal University , Guilin, China
                [3] 3 School of Mechanical and Electrical Engineering, Guilin University of Electronic Technology , Guilin, China
                [4] 4 Golden Camellia National Nature Reserve Management Center , Fangchenggang, China
                [5] 5 Administration of Nonggang National Nature Reserve of Guangxi , Chongzuo, China
                Author notes

                Edited by: Sofia I. A. Pereira, Universidade Católica Portuguesa, Portugal

                Reviewed by: Chuansheng Mei, Institute for Advanced Learning and Research, United States; Jun Rong, Nanchang University, China

                *Correspondence: Shengfeng Chai, sfchai@ 123456163.com ; Yu Liang, liangyu@ 123456gxnu.edu.cn ; Xiao Wei, weixiao@ 123456gxib.cn

                †These authors have contributed equally to this work

                Article
                10.3389/fpls.2023.1180472
                10699447
                38078115
                e36f2442-1641-42f4-a457-eb060747b6a0
                Copyright © 2023 Liu, Jiang, Huang, Zhong, Xu, Yang, Liu, Wei, Liang and Chai

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 06 March 2023
                : 30 October 2023
                Page count
                Figures: 8, Tables: 2, Equations: 0, References: 47, Pages: 15, Words: 7406
                Funding
                This research was supported by the National Natural Science Foundation of China (32060248 and 31660092), the Key Research and Development Program of Guangxi (GuikeAB21196018), the Natural Science Foundation of Guangxi (Grants 2020GXNSFBA297157 and 2020GXNSFBA297045), the Innovation Project of Guangxi Graduate Education (YCSW2023127), the Innovation Training Program for University Students (202210602020), the Sustainable Development Innovation Project and English Course Construction Project for Postgraduates of Guangxi Normal University (2020CX003 and 2021XJQYW01), and the Key Research and Development Project of Guangxi (NO: GuiKeAB22080044).
                Categories
                Plant Science
                Original Research
                Custom metadata
                Plant Symbiotic Interactions

                Plant science & Botany
                golden camellia,adaptation mechanism,karst regions,metagenome,transcriptome
                Plant science & Botany
                golden camellia, adaptation mechanism, karst regions, metagenome, transcriptome

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