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      Phytochemical Composition, Antioxidant Capacity, and Enzyme Inhibitory Activity in Callus, Somaclonal Variant, and Normal Green Shoot Tissues of Catharanthus roseus (L) G. Don

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          Abstract

          This study aimed to investigate the impact of plant growth regulators, sucrose concentration, and the number of subcultures on axillary shoot multiplication, in vitro flowering, and somaclonal variation and to assess the phytochemical composition, antioxidant capacity, and enzyme inhibitory potential of in vitro-established callus, somaclonal variant, and normal green shoots of Catharanthus roseus. The highest shoot induction rate (95.8%) and highest number of shoots (23.6), with a mean length of 4.5 cm, were attained when the C. roseus nodal explants (0.6–1 cm in length) were cultivated in Murashige and Skoog (MS) medium with 2 µM thidiazuron, 1 µM 2-(1-naphthyl) acetic acid (NAA), and 4% sucrose. The in vitro flowering of C. roseus was affected by sucrose, and the number of subcultures had a significant effect on shoot multiplication and somaclonal variation. The highest levels of phenolics and flavonoids were found in normal green shoots, followed by those in somaclonal variant shoots and callus. The phytochemicals in C. roseus extracts were qualified using liquid chromatography–tandem mass spectrometry. A total of 39, 55, and 59 compounds were identified in the callus, somaclonal variant shoot, and normal green shoot tissues, respectively. The normal green shoot extracts exhibited the best free radical scavenging ability and reducing power activity. The strongest acetylcholinesterase inhibitory effects were found in the callus, with an IC50 of 0.65 mg/mL.

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          A Revised Medium for Rapid Growth and Bio Assays with Tobacco Tissue Cultures

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            Sugar demand, not auxin, is the initial regulator of apical dominance.

            For almost a century the plant hormone auxin has been central to theories on apical dominance, whereby the growing shoot tip suppresses the growth of the axillary buds below. According to the classic model, the auxin indole-3-acetic acid is produced in the shoot tip and transported down the stem, where it inhibits bud growth. We report here that the initiation of bud growth after shoot tip loss cannot be dependent on apical auxin supply because we observe bud release up to 24 h before changes in auxin content in the adjacent stem. After the loss of the shoot tip, sugars are rapidly redistributed over large distances and accumulate in axillary buds within a timeframe that correlates with bud release. Moreover, artificially increasing sucrose levels in plants represses the expression of BRANCHED1 (BRC1), the key transcriptional regulator responsible for maintaining bud dormancy, and results in rapid bud release. An enhancement in sugar supply is both necessary and sufficient for suppressed buds to be released from apical dominance. Our data support a theory of apical dominance whereby the shoot tip's strong demand for sugars inhibits axillary bud outgrowth by limiting the amount of sugar translocated to those buds.
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              Medicinal prospects of antioxidants: A review

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                Author and article information

                Journal
                Molecules
                Molecules
                molecules
                Molecules
                MDPI
                1420-3049
                26 October 2020
                November 2020
                : 25
                : 21
                : 4945
                Affiliations
                [1 ]Department of Bioindustry and Bioresource Engineering, Sejong University, 209 Neungdong-ro, Gwangjin-gu, Seoul 05006, Korea; onewlee@ 123456sejong.ac.kr (O.N.L.); hypark@ 123456sejong.ac.kr (H.Y.P.)
                [2 ]Department of Biology, Faculty of Science, Selcuk University, Konya 42130, Turkey; akguneselcuk@ 123456gmail.com (G.A.); gokhanzengin@ 123456selcuk.edu.tr (G.Z.)
                [3 ]Agricultural and Molecular Research and Service Institute, University of Nyíregyháza, 4400 Nyíregyháza, Hungary; cziaky.zoltan@ 123456nye.hu (Z.C.); jjozsi@ 123456gmail.com (J.J.)
                [4 ]Indigenous Knowledge Systems Centre, Faculty of Natural and Agricultural Sciences, North-West University, Private Bag X2046, Mmabatho 2745, North West, South Africa; Ragupathi.Rengasamy@ 123456nwu.ac.za
                [5 ]Department of Bioresources and Food Science, Institute of Natural Science and Agriculture, Konkuk University, Seoul 05029, Korea; kimdh@ 123456konkuk.ac.kr
                Author notes
                [* ]Correspondence: siva74@ 123456konkuk.ac.kr ; Tel.: +82-2450-0576
                Author information
                https://orcid.org/0000-0001-6548-7823
                https://orcid.org/0000-0002-1846-3236
                https://orcid.org/0000-0001-7447-6392
                Article
                molecules-25-04945
                10.3390/molecules25214945
                7663286
                33114628
                a9160bcf-e6c5-4681-a2bb-e84de6d221fe
                © 2020 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 28 September 2020
                : 21 October 2020
                Categories
                Article

                alkaloids,antioxidant activity,in vitro flowering,micropropagation,phenolics,somaclonal variation

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