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      Bacterial-Mediated Salinity Stress Tolerance in Maize ( Zea mays L.): A Fortunate Way toward Sustainable Agriculture

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          Abstract

          Sustainable agriculture is threatened by salinity stress because of the low yield quality and low crop production. Rhizobacteria that promote plant growth modify physiological and molecular pathways to support plant development and reduce abiotic stresses. The recent study aimed to assess the tolerance capacity and impacts of Bacillus sp. PM31 on the growth, physiological, and molecular responses of maize to salinity stress. In comparison to uninoculated plants, the inoculation of Bacillus sp. PM31 improved the agro-morphological traits [shoot length (6%), root length (22%), plant height (16%), fresh weight (39%), dry weight (29%), leaf area (11%)], chlorophyll [Chl a (17%), Chl b (37%), total chl (22%)], carotenoids (15%), proteins (40%), sugars (43%), relative water (11%), flavonoids (22%), phenols (23%), radical scavenging capacity (13%), and antioxidants. The Bacillus sp. PM31-inoculated plants showed a reduction in the oxidative stress indicators [electrolyte leakage (12%), H 2O 2 (9%), and MDA (32%)] as compared to uninoculated plants under salinity and increased the level of osmolytes [free amino acids (36%), glycine betaine (17%), proline (11%)]. The enhancement of plant growth under salinity was further validated by the molecular profiling of Bacillus sp. PM31. Moreover, these physiological and molecular mechanisms were accompanied by the upregulation of stress-related genes (APX and SOD). Our study found that Bacillus sp. PM31 has a crucial and substantial role in reducing salinity stress through physiological and molecular processes, which may be used as an alternative approach to boost crop production and yield.

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          Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method.

          The two most commonly used methods to analyze data from real-time, quantitative PCR experiments are absolute quantification and relative quantification. Absolute quantification determines the input copy number, usually by relating the PCR signal to a standard curve. Relative quantification relates the PCR signal of the target transcript in a treatment group to that of another sample such as an untreated control. The 2(-Delta Delta C(T)) method is a convenient way to analyze the relative changes in gene expression from real-time quantitative PCR experiments. The purpose of this report is to present the derivation, assumptions, and applications of the 2(-Delta Delta C(T)) method. In addition, we present the derivation and applications of two variations of the 2(-Delta Delta C(T)) method that may be useful in the analysis of real-time, quantitative PCR data. Copyright 2001 Elsevier Science (USA).
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            Salt tolerance and salinity effects on plants: a review.

            Plants exposed to salt stress undergo changes in their environment. The ability of plants to tolerate salt is determined by multiple biochemical pathways that facilitate retention and/or acquisition of water, protect chloroplast functions, and maintain ion homeostasis. Essential pathways include those that lead to synthesis of osmotically active metabolites, specific proteins, and certain free radical scavenging enzymes that control ion and water flux and support scavenging of oxygen radicals or chaperones. The ability of plants to detoxify radicals under conditions of salt stress is probably the most critical requirement. Many salt-tolerant species accumulate methylated metabolites, which play crucial dual roles as osmoprotectants and as radical scavengers. Their synthesis is correlated with stress-induced enhancement of photorespiration. In this paper, plant responses to salinity stress are reviewed with emphasis on physiological, biochemical, and molecular mechanisms of salt tolerance. This review may help in interdisciplinary studies to assess the ecological significance of salt stress.
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              Universal chemical assay for the detection and determination of siderophores

              A universal method to detect and determine siderophores was developed by using their high affinity for iron(III). The ternary complex chrome azurol S/iron(III)/hexadecyltrimethylammonium bromide, with an extinction coefficient of approximately 100,000 M-1 cm-1 at 630 nm, serves as an indicator. When a strong chelator removes the iron from the dye, its color turns from blue to orange. Because of the high sensitivity, determination of siderophores in solution and their characterization by paper electrophoresis chromatography can be performed directly on supernatants of culture fluids. The method is also applicable to agar plates. Orange halos around the colonies on blue agar are indicative of siderophore excretion. It was demonstrated with Escherichia coli strains that biosynthetic, transport, and regulatory mutations in the enterobactin system are clearly distinguishable. The method was successfully used to screen mutants in the iron uptake system of two Rhizobium meliloti strains, DM5 and 1021.
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                Author and article information

                Journal
                ACS Omega
                ACS Omega
                ao
                acsodf
                ACS Omega
                American Chemical Society
                2470-1343
                26 May 2023
                13 June 2023
                : 8
                : 23
                : 20471-20487
                Affiliations
                []Department of Plant Sciences, Quaid-i-Azam University , Islamabad, Pakistan 45320
                []Department of Plant Pathology, Federal University of Lavras , Lavras, MG, Brazil 37200-900
                [§ ]Institute of Industrial Biotechnology, Government College University Lahore , Lahore, Pakistan 54000
                []Department of Biotechnology, Quaid-i-Azam University , Islamabad, Pakistan 45320
                []Department of Botany, Government College University Lahore , Lahore, Pakistan 54000
                [# ]Department of Botany, Government College University , Faisalabad 38000, Pakistan
                []Department of Environmental Sciences, Quaid-i-Azam University , Islamabad, Pakistan 45320
                []Department of Botany and Microbiology, College of Science, King Saud University , Riyadh, Saudi Arabia 11451
                []Food Engineering Department, Faculty of Food Science and Technology, University of Agricultural Sciences and Veterinary Medicine of Cluj-Napoca , Cluj-Napoca, Romania 400372
                []Department of Horticulture, Agricultural Faculty, Ataturk Universitesi , Erzurum, Türkiye 25240
                []Ata Teknokent, HGF Agro , TR-25240 Erzurum, Türkiye
                []Botany Department, Faculty of Science, Mansoura University , Mansoura, Egypt 35511
                Author notes
                Author information
                https://orcid.org/0000-0003-1553-2248
                https://orcid.org/0000-0002-6409-6019
                Article
                10.1021/acsomega.3c00723
                10275368
                37332827
                3816cc68-1e14-4b43-8251-eda942bed297
                © 2023 The Authors. Published by American Chemical Society

                Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained ( https://creativecommons.org/licenses/by/4.0/).

                History
                : 06 February 2023
                : 16 May 2023
                Funding
                Funded by: King Saud University, doi 10.13039/501100002383;
                Award ID: RSP2023R173
                Categories
                Article
                Custom metadata
                ao3c00723
                ao3c00723

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