Stress-responsive gene regulation conferring salinity tolerance in wheat inoculated with ACC deaminase producing facultative methylotrophic actinobacterium

被引:9
作者
Meena, Kamlesh K. [1 ]
Sorty, Ajay M. [2 ,3 ]
Bitla, Utkarsh [2 ]
Shinde, Akash L. [2 ]
Kumar, Satish [2 ,4 ]
Wakchaure, Goraksha C. [2 ]
Kumar, Shrvan [1 ]
Kanwat, Manish [1 ]
Singh, Dhananjaya P. [5 ]
机构
[1] Indian Council Agr Res ICAR, Cent Arid Zone Res Inst, Div Integrated Farming Syst, Jodhpur, India
[2] Indian Council Agr Res ICAR, Natl Inst Abiot Stress Management, Sch Soil Stress Management, Baramati, India
[3] Aarhus Univ, Dept Environm Sci Environm Microbiol, Roskilde, Denmark
[4] Indian Council Agr Res ICAR, Dept Biochem, Directorate Onion & Garl Res, Pune, India
[5] Indian Council Agr Res ICAR, Indian Inst Vegetable Res, Crop Improvement Div, Varanasi, India
关键词
salinity stress; ACC deaminase; Nocardioides; methylotrophic bacteria; mitigation; wheat; ABA; Mitigation; AEROBIC METHYLOBACTERIA; PLANT-GROWTH; MICROORGANISMS;
D O I
10.3389/fpls.2023.1249600
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Microbes enhance crop resilience to abiotic stresses, aiding agricultural sustainability amid rising global land salinity. While microbes have proven effective via seed priming, soil amendments, and foliar sprays in diverse crops, their mechanisms remain less explored. This study explores the utilization of ACC deaminase-producing Nocardioides sp. to enhance wheat growth in saline environments and the molecular mechanisms underlying Nocardioides sp.-mediated salinity tolerance in wheat. The Nocardioides sp. inoculated seeds were grown under four salinity regimes viz., 0 dS m(-1), 5 dS m(-1), 10 dS m(-1), and 15 dS m(-1), and vegetative growth parameters including shoot-root length, germination percentage, seedling vigor index, total biomass, and shoot-root ratio were recorded. The Nocardioides inoculated wheat plants performed well under saline conditions compared to uninoculated plants and exhibited lower shoot:root (S:R) ratio (1.52 +/- 0.14 for treated plants against 1.84 +/- 0.08 for untreated plants) at salinity level of 15 dS m(-1) and also showed improved biomass at 5 dS m(-1) and 10 dS m(-1). Furthermore, the inoculated plants also exhibited higher protein content viz., 22.13 mg g(-1), 22.10 mg g(-1), 22.63 mg g(-1), and 23.62 mg g(-1) fresh weight, respectively, at 0 dS m(-1), 5 dS m(-1), 10 dS m(-1), and 15 dS m(-1). The mechanisms were studied in terms of catalase, peroxidase, superoxide dismutase, and ascorbate peroxidase activity, free radical scavenging potential, in-situ localization of H2O2 and superoxide ions, and DNA damage. The inoculated seedlings maintained higher enzymatic and non-enzymatic antioxidant potential, which corroborated with reduced H2O2 and superoxide localization within the tissue. The gene expression profiles of 18 stress-related genes involving abscisic acid signaling, salt overly sensitive (SOS response), ion transporters, stress-related transcription factors, and antioxidant enzymes were also analyzed. Higher levels of stress-responsive gene transcripts, for instance, TaABARE (similar to+7- and +10-fold at 10 dS m(-1) and 15 dS m(-1)); TaHAk1 and hkt1 (similar to+4- and +8-fold at 15 dS m(-1)); antioxidant enzymes CAT, MnSOD, POD, APX, GPX, and GR (similar to+4, +3, +5, +4, +9, and +8 folds and), indicated actively elevated combat mechanisms in inoculated seedlings. Our findings emphasize Nocardioides sp.-mediated wheat salinity tolerance via ABA-dependent cascade and salt-responsive ion transport system. This urges additional study of methylotrophic microbes to enhance crop abiotic stress resilience.
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页数:11
相关论文
共 40 条
[11]   Aerobic methylobacteria are capable of synthesizing auxins [J].
Ivanova, EG ;
Doronina, NV ;
Trotsenko, YA .
MICROBIOLOGY, 2001, 70 (04) :392-397
[12]   Initiation of runaway cell death in an Arabidopsis mutant by extracellular superoxide [J].
Jabs, T ;
Dietrich, RA ;
Dangl, JL .
SCIENCE, 1996, 273 (5283) :1853-1856
[13]   Mitigation of salinity-induced oxidative damage in wheat (Triticum aestivum L.) seedlings by exogenous application of phenolic acids [J].
Kaur, Harsimran ;
Bhardwaj, Rachana D. ;
Grewal, Satvir K. .
ACTA PHYSIOLOGIAE PLANTARUM, 2017, 39 (10)
[14]   Polyphenols, Flavonoids, and Antioxidant Activity Involved in Salt Tolerance in Wheat, Aegilops cylindrica and Their Amphidiploids [J].
Kiani, Razieh ;
Arzani, Ahmad ;
Mirmohammady Maibody, S. A. M. .
FRONTIERS IN PLANT SCIENCE, 2021, 12
[15]   Does plant-Microbe interaction confer stress tolerance in plants: A review? [J].
Kumar, Akhilesh ;
Verma, Jay Prakash .
MICROBIOLOGICAL RESEARCH, 2018, 207 :41-52
[16]  
Li H., 2019, Plant Physiol. Biochem, V143, P153, DOI [10.1016/j.plaphy.2019.08.018, DOI 10.1016/J.PLAPHY.2019.08.018]
[17]   Solvent effects and improvements in the deoxyribose degradation assay for hydroxyl radical-scavenging [J].
Li, Xican .
FOOD CHEMISTRY, 2013, 141 (03) :2083-2088
[18]  
Li Z., 2021, Front. Plant Sci, V12, DOI [10.3389/fpls.2021.667847, DOI 10.3389/FPLS.2021.667847]
[19]  
Luck H., 1971, Methods of enzymatic analysis, V3, P279
[20]  
Madhaiyan M, 2004, BOT BULL ACAD SINICA, V45, P315