Soybean Leaf Proteomic Profile Influenced by Rhizobacteria Under Optimal and Salt Stress Conditions
Soil salinity is a major abiotic stressor inhibiting plant growth and development by affecting a range of physiological processes. Plant growth promoting rhizobacteria (PGPR) are considered a sustainable option for alleviation of stress and enhancement of plant growth, yet their mode of action is co...
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Published in | Frontiers in plant science Vol. 13; p. 809906 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
Frontiers Media S.A
24.03.2022
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Online Access | Get full text |
ISSN | 1664-462X 1664-462X |
DOI | 10.3389/fpls.2022.809906 |
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Abstract | Soil salinity is a major abiotic stressor inhibiting plant growth and development by affecting a range of physiological processes. Plant growth promoting rhizobacteria (PGPR) are considered a sustainable option for alleviation of stress and enhancement of plant growth, yet their mode of action is complex and largely unexplored. In this study, an untargeted proteomic approach provided insights into growth and stress response mechanisms elicited in soybean plants by
Rhizobium
sp. SL42 and
Hydrogenophaga
sp. SL48 and co-inoculated with
Bradyrhizobium japonicum
532C. The plants were grown under optimal and salt-stressed conditions up to their mid-vegetative stage; shoot growth variables were increased in the bacteria-treated plants. Shotgun proteomics of soybean leaf tissue revealed that a number of proteins related to plant growth and stress tolerance were modulated in the bacterial inoculation treatments. Several key proteins involved in major metabolic pathways of photosynthesis, respiration, and photorespiration were upregulated. These include photosystem I psaK, Rubisco subunits, glyceraldehyde-3-phosphate dehydrogenase, succinate dehydrogenase, and glycine decarboxylase. Similarly, stress response proteins such as catalase and glutathione S-transferase (antioxidants), proline-rich precursor protein (osmolyte), and NADP-dependent malic enzyme (linked to ABA signaling) were increased under salt stress. The functions of proteins related to plant growth and stress adaptation led to an expanded understanding of plant-microbe interactions. These findings suggest that the PGPR strains regulated proteome expression in soybean leaves through multiple signaling pathways, thereby inducing salinity tolerance, and improving plant growth in the presence of this abiotic stress challenge. Data are available
via
ProteomeXchange with identifier PXD025596. |
---|---|
AbstractList | Soil salinity is a major abiotic stressor inhibiting plant growth and development by affecting a range of physiological processes. Plant growth promoting rhizobacteria (PGPR) are considered a sustainable option for alleviation of stress and enhancement of plant growth, yet their mode of action is complex and largely unexplored. In this study, an untargeted proteomic approach provided insights into growth and stress response mechanisms elicited in soybean plants by
Rhizobium
sp. SL42 and
Hydrogenophaga
sp. SL48 and co-inoculated with
Bradyrhizobium japonicum
532C. The plants were grown under optimal and salt-stressed conditions up to their mid-vegetative stage; shoot growth variables were increased in the bacteria-treated plants. Shotgun proteomics of soybean leaf tissue revealed that a number of proteins related to plant growth and stress tolerance were modulated in the bacterial inoculation treatments. Several key proteins involved in major metabolic pathways of photosynthesis, respiration, and photorespiration were upregulated. These include photosystem I psaK, Rubisco subunits, glyceraldehyde-3-phosphate dehydrogenase, succinate dehydrogenase, and glycine decarboxylase. Similarly, stress response proteins such as catalase and glutathione S-transferase (antioxidants), proline-rich precursor protein (osmolyte), and NADP-dependent malic enzyme (linked to ABA signaling) were increased under salt stress. The functions of proteins related to plant growth and stress adaptation led to an expanded understanding of plant-microbe interactions. These findings suggest that the PGPR strains regulated proteome expression in soybean leaves through multiple signaling pathways, thereby inducing salinity tolerance, and improving plant growth in the presence of this abiotic stress challenge. Data are available
via
ProteomeXchange with identifier PXD025596. Soil salinity is a major abiotic stressor inhibiting plant growth and development by affecting a range of physiological processes. Plant growth promoting rhizobacteria (PGPR) are considered a sustainable option for alleviation of stress and enhancement of plant growth, yet their mode of action is complex and largely unexplored. In this study, an untargeted proteomic approach provided insights into growth and stress response mechanisms elicited in soybean plants by Rhizobium sp. SL42 and Hydrogenophaga sp. SL48 and co-inoculated with Bradyrhizobium japonicum 532C. The plants were grown under optimal and salt-stressed conditions up to their mid-vegetative stage; shoot growth variables were increased in the bacteria-treated plants. Shotgun proteomics of soybean leaf tissue revealed that a number of proteins related to plant growth and stress tolerance were modulated in the bacterial inoculation treatments. Several key proteins involved in major metabolic pathways of photosynthesis, respiration, and photorespiration were upregulated. These include photosystem I psaK, Rubisco subunits, glyceraldehyde-3-phosphate dehydrogenase, succinate dehydrogenase, and glycine decarboxylase. Similarly, stress response proteins such as catalase and glutathione S-transferase (antioxidants), proline-rich precursor protein (osmolyte), and NADP-dependent malic enzyme (linked to ABA signaling) were increased under salt stress. The functions of proteins related to plant growth and stress adaptation led to an expanded understanding of plant-microbe interactions. These findings suggest that the PGPR strains regulated proteome expression in soybean leaves through multiple signaling pathways, thereby inducing salinity tolerance, and improving plant growth in the presence of this abiotic stress challenge. Data are available via ProteomeXchange with identifier PXD025596. Soil salinity is a major abiotic stressor inhibiting plant growth and development by affecting a range of physiological processes. Plant growth promoting rhizobacteria (PGPR) are considered a sustainable option for alleviation of stress and enhancement of plant growth, yet their mode of action is complex and largely unexplored. In this study, an untargeted proteomic approach provided insights into growth and stress response mechanisms elicited in soybean plants by Rhizobium sp. SL42 and Hydrogenophaga sp. SL48 and co-inoculated with Bradyrhizobium japonicum 532C. The plants were grown under optimal and salt-stressed conditions up to their mid-vegetative stage; shoot growth variables were increased in the bacteria-treated plants. Shotgun proteomics of soybean leaf tissue revealed that a number of proteins related to plant growth and stress tolerance were modulated in the bacterial inoculation treatments. Several key proteins involved in major metabolic pathways of photosynthesis, respiration, and photorespiration were upregulated. These include photosystem I psaK, Rubisco subunits, glyceraldehyde-3-phosphate dehydrogenase, succinate dehydrogenase, and glycine decarboxylase. Similarly, stress response proteins such as catalase and glutathione S-transferase (antioxidants), proline-rich precursor protein (osmolyte), and NADP-dependent malic enzyme (linked to ABA signaling) were increased under salt stress. The functions of proteins related to plant growth and stress adaptation led to an expanded understanding of plant-microbe interactions. These findings suggest that the PGPR strains regulated proteome expression in soybean leaves through multiple signaling pathways, thereby inducing salinity tolerance, and improving plant growth in the presence of this abiotic stress challenge. Data are available via ProteomeXchange with identifier PXD025596.Soil salinity is a major abiotic stressor inhibiting plant growth and development by affecting a range of physiological processes. Plant growth promoting rhizobacteria (PGPR) are considered a sustainable option for alleviation of stress and enhancement of plant growth, yet their mode of action is complex and largely unexplored. In this study, an untargeted proteomic approach provided insights into growth and stress response mechanisms elicited in soybean plants by Rhizobium sp. SL42 and Hydrogenophaga sp. SL48 and co-inoculated with Bradyrhizobium japonicum 532C. The plants were grown under optimal and salt-stressed conditions up to their mid-vegetative stage; shoot growth variables were increased in the bacteria-treated plants. Shotgun proteomics of soybean leaf tissue revealed that a number of proteins related to plant growth and stress tolerance were modulated in the bacterial inoculation treatments. Several key proteins involved in major metabolic pathways of photosynthesis, respiration, and photorespiration were upregulated. These include photosystem I psaK, Rubisco subunits, glyceraldehyde-3-phosphate dehydrogenase, succinate dehydrogenase, and glycine decarboxylase. Similarly, stress response proteins such as catalase and glutathione S-transferase (antioxidants), proline-rich precursor protein (osmolyte), and NADP-dependent malic enzyme (linked to ABA signaling) were increased under salt stress. The functions of proteins related to plant growth and stress adaptation led to an expanded understanding of plant-microbe interactions. These findings suggest that the PGPR strains regulated proteome expression in soybean leaves through multiple signaling pathways, thereby inducing salinity tolerance, and improving plant growth in the presence of this abiotic stress challenge. Data are available via ProteomeXchange with identifier PXD025596. Soil salinity is a major abiotic stressor inhibiting plant growth and development by affecting a range of physiological processes. Plant growth promoting rhizobacteria (PGPR) are considered a sustainable option for alleviation of stress and enhancement of plant growth, yet their mode of action is complex and largely unexplored. In this study, an untargeted proteomic approach provided insights into growth and stress response mechanisms elicited in soybean plants by sp. SL42 and sp. SL48 and co-inoculated with 532C. The plants were grown under optimal and salt-stressed conditions up to their mid-vegetative stage; shoot growth variables were increased in the bacteria-treated plants. Shotgun proteomics of soybean leaf tissue revealed that a number of proteins related to plant growth and stress tolerance were modulated in the bacterial inoculation treatments. Several key proteins involved in major metabolic pathways of photosynthesis, respiration, and photorespiration were upregulated. These include photosystem I psaK, Rubisco subunits, glyceraldehyde-3-phosphate dehydrogenase, succinate dehydrogenase, and glycine decarboxylase. Similarly, stress response proteins such as catalase and glutathione S-transferase (antioxidants), proline-rich precursor protein (osmolyte), and NADP-dependent malic enzyme (linked to ABA signaling) were increased under salt stress. The functions of proteins related to plant growth and stress adaptation led to an expanded understanding of plant-microbe interactions. These findings suggest that the PGPR strains regulated proteome expression in soybean leaves through multiple signaling pathways, thereby inducing salinity tolerance, and improving plant growth in the presence of this abiotic stress challenge. Data are available ProteomeXchange with identifier PXD025596. |
Author | Smith, Donald L. Ilangumaran, Gayathri Subramanian, Sowmyalakshmi |
AuthorAffiliation | Department of Plant Science, McGill University, Montréal , QC , Canada |
AuthorAffiliation_xml | – name: Department of Plant Science, McGill University, Montréal , QC , Canada |
Author_xml | – sequence: 1 givenname: Gayathri surname: Ilangumaran fullname: Ilangumaran, Gayathri – sequence: 2 givenname: Sowmyalakshmi surname: Subramanian fullname: Subramanian, Sowmyalakshmi – sequence: 3 givenname: Donald L. surname: Smith fullname: Smith, Donald L. |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/35401626$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1016_j_apsoil_2023_105056 crossref_primary_10_1007_s10123_023_00469_4 crossref_primary_10_1007_s11756_024_01689_3 crossref_primary_10_3389_fpls_2022_1101862 crossref_primary_10_3390_ijms26020565 crossref_primary_10_1039_D3EN00368J crossref_primary_10_1016_j_scitotenv_2025_178413 crossref_primary_10_1007_s00425_023_04310_0 crossref_primary_10_1016_j_scitotenv_2023_164260 crossref_primary_10_1016_j_plaphy_2023_108080 crossref_primary_10_3389_frmbi_2024_1309947 |
Cites_doi | 10.1104/pp.15.00858 10.1111/j.1365-313X.2010.04425.x 10.1111/nph.13519 10.1007/s00122-001-0853-5 10.1105/tpc.109.070201 10.1105/tpc.105.033365 10.1079/Ssr2002108 10.1146/annurev.arplant.53.091401.143329 10.3390/plants3030324 10.1016/j.phytochem.2012.09.017 10.1111/plb.12884 10.1007/s11103-016-0542-z 10.1093/aob/mcu267 10.1002/ldr.3005 10.1016/j.soilbio.2004.08.030 10.1023/A:1022352229863 10.1007/s00425-006-0423-9 10.3389/fpls.2015.00722 10.1104/pp.17.00970 10.1007/978-94-017-7758-2_4 10.1105/tpc.002477 10.1038/srep39024 10.1093/nar/gkw419 10.1023/b:plan.0000004307.62398.91 10.1105/tpc.113.115659 10.1016/j.plaphy.2018.09.026 10.1007/s00299-011-1081-3 10.3389/fsufs.2020.617978 10.1186/1756-0500-7-643 10.1111/j.1365-3040.2012.02576.x 10.1046/j.1365-313X.2001.01095.x 10.1021/ac025747h 10.1104/pp.001784 10.3389/fpls.2018.01637 10.1105/tpc.104.022046 10.1093/nar/gky1106 10.1023/A:1004203018770 10.1007/s11356-018-1610-5 10.1111/jam.12866 10.1007/s12374-020-09241-x 10.1155/2019/9530963 10.1038/srep24212 10.1146/annurev.arplant.59.032607.092911 10.1007/s00425-011-1425-9 10.1111/j.1744-7909.2008.00760.x 10.1042/Bj20090775 10.1007/0-387-25856-6_9 10.1042/Bcj20190435 10.1080/17429145.2014.894587 10.1021/ac0341261 10.1371/journal.pone.0006648 |
ContentType | Journal Article |
Copyright | Copyright © 2022 Ilangumaran, Subramanian and Smith. Copyright © 2022 Ilangumaran, Subramanian and Smith. 2022 Ilangumaran, Subramanian and Smith |
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Keywords | soybean leaf proteomics salinity signaling pathways stress response PGPR |
Language | English |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Reviewed by: Om Prakash Narayan, Tufts University, United States; Shekhar Jain, Mandsaur University, India This article was submitted to Plant Proteomics and Protein Structural Biology, a section of the journal Frontiers in Plant Science Edited by: Alex Jones, University of Warwick, United Kingdom |
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References | Waśkiewicz (B46) 2016 Oh (B32) 2014; 7 Wang (B45) 2016; 6 Germain (B11) 2001 Bergmuller (B5) 2003; 52 Tromas (B42) 2009; 4 Gonzalez-Guzman (B13) 2002; 14 Keller (B20) 2002; 74 Khan (B21); 2019 Pou (B35) 2016; 92 Gaufichon (B10) 2013; 36 Taira (B41) 2004; 16 Ilangumaran (B17) 2021; 4 Kang (B19) 2014; 9 (B39) 2020 Zorb (B53) 2019; 21 Nesvizhskii (B30) 2003; 75 Vaishnav (B43) 2015; 119 Larson (B23) 2017; 175 Flowers (B9) 2015; 115 Linkies (B24) 2009; 21 Ning (B31) 2018; 29 Munns (B29) 2008; 59 Perez-Riverol (B33) 2019; 47 Arias (B2) 2018; 9 Hosseini (B16) 2002; 12 Carranza (B6) 2016; 6 Babicki (B3) 2016; 44 Khan (B22); 476 Viswanath (B44) 2020; 63 Xu (B47) 2011; 234 El-Esawi (B8) 2018; 132 Gray (B14) 2005; 37 Stepanova (B40) 2005; 17 Marr (B25) 1997; 189 Molla-Morales (B27) 2011; 65 Zhu (B52) 2002; 53 Zhong (B51) 2015; 169 Gisk (B12) 2010; 425 He (B15) 2002; 104 Martins (B26) 2018; 25 Phang (B34) 2008; 50 Zhang (B50) 2013; 85 Chinnusamy (B7) 2006; 27 Battaglia (B4) 2007; 225 Xu (B48) 2002; 129 Abrol (B1) 1988 Jiang (B18) 2013; 25 Sanchez-Parra (B37) 2014; 3 Munns (B28) 2015; 208 Rashid (B36) 2011; 30 Smith (B38) 2015; 6 Zhang (B49) 2003; 248 |
References_xml | – volume: 169 start-page: 2288 year: 2015 ident: B51 article-title: Gibberellic acid-stimulated Arabidopsis6 serves as an integrator of gibberellin, abscisic acid, and glucose signaling during seed germination in Arabidopsis. publication-title: Plant Physiol. doi: 10.1104/pp.15.00858 – volume: 65 start-page: 335 year: 2011 ident: B27 article-title: Analysis of ven3 and ven6 reticulate mutants reveals the importance of arginine biosynthesis in Arabidopsis leaf development. publication-title: Plant J. doi: 10.1111/j.1365-313X.2010.04425.x – volume: 208 start-page: 668 year: 2015 ident: B28 article-title: Salinity tolerance of crops - what is the cost? publication-title: New Phytol. doi: 10.1111/nph.13519 – volume: 104 start-page: 1125 year: 2002 ident: B15 article-title: A soybean gene encoding a proline-rich protein is regulated by salicylic acid, an endogenous circadian rhythm and by various stresses. publication-title: Theor. Appl. Genet. doi: 10.1007/s00122-001-0853-5 – volume: 21 start-page: 3803 year: 2009 ident: B24 article-title: Ethylene interacts with abscisic acid to regulate endosperm rupture during germination: a comparative approach using Lepidium sativum and Arabidopsis thaliana. publication-title: Plant Cell doi: 10.1105/tpc.109.070201 – volume: 17 start-page: 2230 year: 2005 ident: B40 article-title: A link between ethylene and auxin uncovered by the characterization of two root-specific ethylene-insensitive mutants in Arabidopsis. publication-title: Plant Cell doi: 10.1105/tpc.105.033365 – volume: 12 start-page: 165 year: 2002 ident: B16 article-title: Comparison of the seed germination and early seedling growth of soybean in saline conditions. publication-title: Seed Sci. Res. doi: 10.1079/Ssr2002108 – volume: 53 start-page: 247 year: 2002 ident: B52 article-title: Salt and drought stress signal transduction in plants. publication-title: Annu. Rev. Plant Biol. doi: 10.1146/annurev.arplant.53.091401.143329 – volume: 3 start-page: 324 year: 2014 ident: B37 article-title: Characterization of four bifunctional plant iam/pam-amidohydrolases capable of contributing to auxin biosynthesis. publication-title: Plants doi: 10.3390/plants3030324 – volume: 85 start-page: 30 year: 2013 ident: B50 article-title: Characterization of Arabidopsis serine:glyoxylate aminotransferase, AGT1, as an asparagine aminotransferase. publication-title: Phytochemistry doi: 10.1016/j.phytochem.2012.09.017 – volume: 21 start-page: 31 year: 2019 ident: B53 article-title: Salinity and crop yield. publication-title: Plant Biol. doi: 10.1111/plb.12884 – volume: 92 start-page: 731 year: 2016 ident: B35 article-title: Salinity-mediated transcriptional and post-translational regulation of the Arabidopsis aquaporin PIP2;7. publication-title: Plant Mol. Biol. doi: 10.1007/s11103-016-0542-z – year: 1988 ident: B1 publication-title: Salt-Affected Soils and their Management [Online]. – volume: 115 start-page: 327 year: 2015 ident: B9 article-title: Plant salt tolerance: adaptations in halophytes. publication-title: Ann. Bot. doi: 10.1093/aob/mcu267 – volume: 29 start-page: 2707 year: 2018 ident: B31 article-title: Physiological and transcriptional responses to salt stress in salt-tolerant and salt-sensitive soybean (Glycine max [L.] Merr.) seedlings. publication-title: Land Degrad. Dev. doi: 10.1002/ldr.3005 – volume: 37 start-page: 395 year: 2005 ident: B14 article-title: Intracellular and extracellular PGPR: commonalities and distinctions in the plant-bacterium signaling processes. publication-title: Soil Biol. Biochem. doi: 10.1016/j.soilbio.2004.08.030 – volume: 248 start-page: 305 year: 2003 ident: B49 article-title: Using competitive and facilitative interactions in intercropping systems enhances crop productivity and nutrient-use efficiency. publication-title: Plant Soil doi: 10.1023/A:1022352229863 – volume: 225 start-page: 1121 year: 2007 ident: B4 article-title: Proline-rich cell wall proteins accumulate in growing regions and phloem tissue in response to water deficit in common bean seedlings. publication-title: Planta doi: 10.1007/s00425-006-0423-9 – volume: 6 year: 2015 ident: B38 article-title: Inter-organismal signaling and management of the phytomicrobiome. publication-title: Front. Plant Sci. doi: 10.3389/fpls.2015.00722 – volume: 175 start-page: 708 year: 2017 ident: B23 article-title: Clathrin heavy chain subunits coordinate endo- and exocytic traffic and affect stomatal movement. publication-title: Plant Physiol. doi: 10.1104/pp.17.00970 – start-page: 75 year: 2016 ident: B46 article-title: Participation of phytohormones in adaptation to salt stress publication-title: Plant Hormones Under Challenging Environmental Factors doi: 10.1007/978-94-017-7758-2_4 – volume: 14 start-page: 1833 year: 2002 ident: B13 article-title: The short-chain alcohol dehydrogenase ABA2 catalyzes the conversion of xanthoxin to abscisic aldehyde. publication-title: Plant Cell doi: 10.1105/tpc.002477 – volume: 6 year: 2016 ident: B45 article-title: Comparative proteomics reveals that phosphorylation of beta carbonic anhydrase 1 might be important for adaptation to drought stress in Brassica napus. publication-title: Sci. Rep. doi: 10.1038/srep39024 – volume: 44 start-page: W147 year: 2016 ident: B3 article-title: Heatmapper: web-enabled heat mapping for all. publication-title: Nucleic Acids Res. doi: 10.1093/nar/gkw419 – volume: 52 start-page: 1181 year: 2003 ident: B5 article-title: Characterization of an Arabidopsis mutant deficient in gamma-tocopherol methyltransferase. publication-title: Plant Mol. Biol. doi: 10.1023/b:plan.0000004307.62398.91 – volume: 25 start-page: 3535 year: 2013 ident: B18 article-title: An Arabidopsis soil-salinity-tolerance mutation confers ethylene-mediated enhancement of sodium/potassium homeostasis. publication-title: Plant Cell doi: 10.1105/tpc.113.115659 – volume: 132 start-page: 375 year: 2018 ident: B8 article-title: Bacillus firmus (SW5) augments salt tolerance in soybean (Glycine max L.) by modulating root system architecture, antioxidant defense systems and stress-responsive genes expression. publication-title: Plant Physiol. Biochem. doi: 10.1016/j.plaphy.2018.09.026 – volume: 30 start-page: 1735 year: 2011 ident: B36 article-title: PELPK1 (At5g09530) contains a unique pentapeptide repeat and is a positive regulator of germination in Arabidopsis thaliana. publication-title: Plant Cell Rep. doi: 10.1007/s00299-011-1081-3 – volume: 4 year: 2021 ident: B17 article-title: Rhizobacteria from root nodules of an indigenous legume enhance salinity stress tolerance in soybean. publication-title: Front. Sustain. Food Syst. doi: 10.3389/fsufs.2020.617978 – volume: 7 year: 2014 ident: B32 article-title: Cosuppression of the chloroplast localized molecular chaperone HSP90.5 impairs plant development and chloroplast biogenesis in Arabidopsis. publication-title: BMC Res. Notes doi: 10.1186/1756-0500-7-643 – volume: 36 start-page: 328 year: 2013 ident: B10 article-title: Arabidopsis thaliana ASN2 encoding asparagine synthetase is involved in the control of nitrogen assimilation and export during vegetative growth. publication-title: Plant Cell Environ. doi: 10.1111/j.1365-3040.2012.02576.x – start-page: 1 year: 2001 ident: B11 article-title: Requirement for 3-ketoacyl-CoA thiolase-2 in peroxisome development, fatty acid beta-oxidation and breakdown of triacylglycerol in lipid bodies of Arabidopsis seedlings. publication-title: Plant J. doi: 10.1046/j.1365-313X.2001.01095.x – volume: 74 start-page: 5383 year: 2002 ident: B20 article-title: Empirical statistical model to estimate the accuracy of peptide identifications made by MS/MS and database search. publication-title: Anal. Chem. doi: 10.1021/ac025747h – volume: 129 start-page: 1285 year: 2002 ident: B48 article-title: Cloning and characterization of the abscisic acid-specific glucosyltransferase gene from adzuki bean seedlings. publication-title: Plant Physiol. doi: 10.1104/pp.001784 – volume: 9 year: 2018 ident: B2 article-title: NADP-dependent malic enzyme 1 participates in the abscisic acid response in Arabidopsis thaliana. publication-title: Front. Plant Sci. doi: 10.3389/fpls.2018.01637 – volume: 16 start-page: 2048 year: 2004 ident: B41 article-title: Arabidopsis thaliana GLN2-encoded glutamine synthetase is dual targeted to leaf mitochondria and chloroplasts. publication-title: Plant Cell doi: 10.1105/tpc.104.022046 – volume: 47 start-page: D442 year: 2019 ident: B33 article-title: The PRIDE database and related tools and resources in 2019: improving support for quantification data. publication-title: Nucleic Acids Res. doi: 10.1093/nar/gky1106 – volume: 189 start-page: 181 year: 1997 ident: B25 article-title: Nodulation restrictive genotypes of Glycine and Amphicarpaea: a comparative analysis. publication-title: Plant Soil doi: 10.1023/A:1004203018770 – volume: 25 start-page: 13676 year: 2018 ident: B26 article-title: Plant-associated bacteria mitigate drought stress in soybean. publication-title: Environ. Sci. Pollut. R. doi: 10.1007/s11356-018-1610-5 – volume: 119 start-page: 539 year: 2015 ident: B43 article-title: Putative bacterial volatile-mediated growth in soybean (Glycine max L. Merrill) and expression of induced proteins under salt stress. publication-title: J. Appl. Microbiol. doi: 10.1111/jam.12866 – volume: 63 start-page: 83 year: 2020 ident: B44 article-title: Plant lipoxygenases and their role in plant physiology. publication-title: J. Plant. Biol. doi: 10.1007/s12374-020-09241-x – volume: 2019 start-page: 1 ident: B21 article-title: Halotolerant rhizobacterial strains mitigate the adverse effects of NaCl stress in soybean seedlings. publication-title: Biomed. Res. Int doi: 10.1155/2019/9530963 – volume: 6 year: 2016 ident: B6 article-title: Hydrolases of the ILR1-like family of Arabidopsis thaliana modulate auxin response by regulating auxin homeostasis in the endoplasmic reticulum. publication-title: Sci. Rep. doi: 10.1038/srep24212 – volume: 59 start-page: 651 year: 2008 ident: B29 article-title: Mechanisms of salinity tolerance. publication-title: Annu. Rev. Plant Biol. doi: 10.1146/annurev.arplant.59.032607.092911 – year: 2020 ident: B39 publication-title: International: World Soybean Production [Online]. – volume: 234 start-page: 565 year: 2011 ident: B47 article-title: The HyPRP gene EARLI1 has an auxiliary role for germinability and early seedling development under low temperature and salt stress conditions in Arabidopsis thaliana. publication-title: Planta doi: 10.1007/s00425-011-1425-9 – volume: 50 start-page: 1196 year: 2008 ident: B34 article-title: Salt tolerance in soybean. publication-title: J. Integr. Plant Biol. doi: 10.1111/j.1744-7909.2008.00760.x – volume: 425 start-page: 425 year: 2010 ident: B12 article-title: Characterization of the haem oxygenase protein family in Arabidopsis thaliana reveals a diversity of functions. publication-title: Biochem. J. doi: 10.1042/Bj20090775 – volume: 27 start-page: 141 year: 2006 ident: B7 article-title: Salt stress signaling and mechanisms of plant salt tolerance. publication-title: Genet. Eng. doi: 10.1007/0-387-25856-6_9 – volume: 476 start-page: 2393 ident: B22 article-title: Rhizobacteria AK1 remediates the toxic effects of salinity stress via regulation of endogenous phytohormones and gene expression in soybean. publication-title: Biochem. J. doi: 10.1042/Bcj20190435 – volume: 9 start-page: 673 year: 2014 ident: B19 article-title: Plant growth-promoting rhizobacteria reduce adverse effects of salinity and osmotic stress by regulating phytohormones and antioxidants in Cucumis sativus. publication-title: J. Plant Interact. doi: 10.1080/17429145.2014.894587 – volume: 75 start-page: 4646 year: 2003 ident: B30 article-title: A statistical model for identifying proteins by tandem mass spectrometry. publication-title: Anal. Chem. doi: 10.1021/ac0341261 – volume: 4 year: 2009 ident: B42 article-title: The AUXIN BINDING PROTEIN 1 is required for differential auxin responses mediating root growth. publication-title: PLoS One doi: 10.1371/journal.pone.0006648 |
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Title | Soybean Leaf Proteomic Profile Influenced by Rhizobacteria Under Optimal and Salt Stress Conditions |
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