Mohammad Danish, Mohammad Shahid, Sobhy M Ibrahim, Lukman Ahamad
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Inoculation with Co-tolerant SRB-5 alleviated cobalt toxicity and significantly enhanced the physiological and biochemical properties of plants. Notably, SRB-5 increased root length (19.2%), root biomass (29%), seedling vigor index (18.4%), total chlorophyll (52%), nodule biomass (41%), leghaemoglobin content (38%), root nitrogen (27%), and phosphorous content (19.3%) in 1000 ppm Co-stressed peas. Additionally, bacterial inoculation reduced proline, malondialdehyde (MDA), hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>), and membrane injury by 85%, 57.3%, 90%, and 75%, respectively, in 1000 ppm Co-exposed plants. Priming with SRB-5 also reduced cobalt uptake in roots (88%), shoots (53.7%), and grains (79.6%) compared to uninoculated treatments. Metal-tolerant beneficial soil bacteria, such as Klebsiella sp. strain SRB-5, could serve as an effective alternative for enhancing pea production in metal-contaminated soils. 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引用次数: 0
摘要
农业土壤中过量的钴(Co)含量会造成严重的毒性,降低作物生长和产量。本研究旨在评估克雷伯氏菌SRB-5的潜力。OR715782),在钴胁迫下减轻钴毒性和促进园豌豆生长。菌株SRB-5耐4000ppm Co(II),在钴胁迫下产生包括吲哚-3-乙酸(IAA)、氨、铁载体、ACC脱氨酶和可溶性磷酸盐在内的生长调节物质。SRB-5吸附Co-(II)的最佳条件为25°C, pH 6.0,孵育时间72 h。通过接种在1000ppm、2000ppm和3000ppm Co-(II)处理的土壤中生长的豌豆,测试了该菌株减轻Co-(II)毒性的能力。接种抗钴性强的SRB-5可以减轻植株的钴毒性,显著提高植株的生理生化性能。SRB-5显著提高了1000ppm co -胁迫豌豆的根长(19.2%)、根生物量(29%)、幼苗活力指数(18.4%)、总叶绿素(52%)、根瘤生物量(41%)、豆血红蛋白含量(38%)、根氮(27%)和磷含量(19.3%)。此外,在1000ppm共暴露的植物中,细菌接种使脯氨酸、丙二醛(MDA)、过氧化氢(H2O2)和膜损伤分别降低了85%、57.3%、90%和75%。与未接种处理相比,SRB-5也降低了根(88%)、芽(53.7%)和籽粒(79.6%)对钴的吸收。克雷伯氏菌SRB-5等耐金属土壤有益菌可作为金属污染土壤中提高豌豆产量的有效替代菌。在未来的农业实践中,使用共耐受性PGPR菌株作为生物肥料具有发展潜力。
Enhancing Pea Plant Growth, Nutrient Acquisition, and Symbiosis in Cobalt-Stressed Soil Using Metal-Tolerant Klebsiella sp.
Excessive cobalt (Co) levels in agricultural soil cause significant toxicity, reducing crop growth and yield. This study aimed to assess the potential of Klebsiella sp. SRB-5 (Accession no. OR715782), in mitigating cobalt toxicity and enhancing the growth of garden peas under cobalt stress. Strain SRB-5, tolerant to 4000 ppm of Co(II), was evaluated for producing growth-regulating substances, including indole-3-acetic acid (IAA), ammonia, siderophore, ACC deaminase, and solubilized phosphate, under cobalt stress. The optimal conditions for Co-(II) biosorption by SRB-5 were determined to be 25°C, pH 6.0, and an incubation time of 72 h. The strain's ability to mitigate Co-(II) toxicity was tested by inoculating peas grown in soil treated with 1000, 2000, and 3000 ppm Co-(II). Inoculation with Co-tolerant SRB-5 alleviated cobalt toxicity and significantly enhanced the physiological and biochemical properties of plants. Notably, SRB-5 increased root length (19.2%), root biomass (29%), seedling vigor index (18.4%), total chlorophyll (52%), nodule biomass (41%), leghaemoglobin content (38%), root nitrogen (27%), and phosphorous content (19.3%) in 1000 ppm Co-stressed peas. Additionally, bacterial inoculation reduced proline, malondialdehyde (MDA), hydrogen peroxide (H2O2), and membrane injury by 85%, 57.3%, 90%, and 75%, respectively, in 1000 ppm Co-exposed plants. Priming with SRB-5 also reduced cobalt uptake in roots (88%), shoots (53.7%), and grains (79.6%) compared to uninoculated treatments. Metal-tolerant beneficial soil bacteria, such as Klebsiella sp. strain SRB-5, could serve as an effective alternative for enhancing pea production in metal-contaminated soils. The use of Co-tolerant PGPR strains holds potential for development as biofertilizers in future agricultural practices.
期刊介绍:
The Journal of Basic Microbiology (JBM) publishes primary research papers on both procaryotic and eucaryotic microorganisms, including bacteria, archaea, fungi, algae, protozoans, phages, viruses, viroids and prions.
Papers published deal with:
microbial interactions (pathogenic, mutualistic, environmental),
ecology,
physiology,
genetics and cell biology/development,
new methodologies, i.e., new imaging technologies (e.g. video-fluorescence microscopy, modern TEM applications)
novel molecular biology methods (e.g. PCR-based gene targeting or cassettes for cloning of GFP constructs).