A halotolerant plant growth promoting consortium of Bacillus sp. RB3 and Pseudomonas sp. EB3 primes banana, Musa acuminata cv. Berangan, against salinity and Foc-TR4 stresses

IF 5.4 Q1 PLANT SCIENCES
Abdussabur M. Kaleh , Pooja Singh , Purabi Mazumdar , Gwo Rong Wong , Kah Ooi Chua , Jennifer Ann Harikrishna
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引用次数: 0

Abstract

A plant-growth promoting bacterial consortium of halotolerant Bacillus sp. and Pseudomonas sp. was evaluated for the ability to prime banana (Musa acuminata cv. Berangan) plants against abiotic (salinity) and biotic (Foc-TR4) stress challenges. PGPB consortium-primed banana plants showed better growth (plant height, root length and root biomass) and improved physiological parameters (relative water content, chlorophyll, and carotenoid contents) in both stressed conditions compared to non-primed banana plants. In addition, primed banana plants showed a reduction in lipid peroxidation and an increase in proline and antioxidant enzymatic activities (superoxide dismutase, catalase, ascorbate peroxidase, peroxidase, and glutathione reductase). In salt-stress conditions (sea salt at 100 mM NaCl equivalent), primed plants showed higher levels of K+, Ca2+, and Mg2+ and lower levels of Cl- and Na+ compared to non-primed salt-stressed plants. Under Foc-TR4 stress, the primed plants showed significant enhancement in the levels of total soluble phenolics, lignin content and defense-related enzyme activities (β-1, 3-glucanase, phenylalanine ammonia lyase, chitinase, polyphenol oxidase, and lipoxygenase). Expression analysis of nine stress-responsive MaWRKY genes (MaWRKY4, MaWRKY23, MaWRKY24, MaWRKY25, MaWRKY28, MaWRKY45, MaWRKY65, MaWRKY89 and MaWRKY145) showed significant upregulation in primed banana plants under salt and Foc-TR4 stresses compared to non-primed plants. These results demonstrate that inoculation with the PGPB consortium improved banana plant growth characteristics and primed WRKY-mediated protection against abiotic and biotic stresses.

芽孢杆菌sp. RB3和假单胞菌sp. EB3诱导香蕉耐盐植物生长促进联合体。Berangan,抗盐度和focc - tr4胁迫
评估了耐盐芽孢杆菌和假单胞菌的植物生长促进细菌群落对香蕉(Musa acuminata cv.Beragan)植物抵御非生物(盐度)和生物(Foc-TR4)胁迫挑战的能力。与未引发的香蕉植物相比,PGPB联合引发的香蕉植株在两种胁迫条件下都表现出更好的生长(株高、根长和根生物量)和改善的生理参数(相对含水量、叶绿素和类胡萝卜素含量)。此外,经过处理的香蕉植物表现出脂质过氧化减少,脯氨酸和抗氧化酶活性(超氧化物歧化酶、过氧化氢酶、抗坏血酸过氧化物酶、过氧化物酶和谷胱甘肽还原酶)增加。在盐胁迫条件下(100 mM NaCl当量的海盐),与未引发的盐胁迫植物相比,引发的植物表现出更高水平的K+、Ca2+和Mg2+,以及更低水平的Cl-和Na+。在Foc-TR4胁迫下,引发植物的总可溶性酚类物质、木质素含量和防御相关酶活性(β-1,3-葡聚糖酶、苯丙氨酸解氨酶、几丁质酶、多酚氧化酶和脂氧合酶)水平显著提高。9个应激反应性MaWRKY基因(MaWRKY4、MaWRKY23、MaWRKY24、MaWRKY25、MaWRKY 28、MaWR京都45、MaWR肯塔基65、MaWRsky 89和MaWRKY145)的表达分析显示,与未引发的植物相比,引发的香蕉植物在盐和Foc-TR4胁迫下显著上调。这些结果表明,用PGPB联合体接种改善了香蕉植物的生长特性,并启动了WRKY介导的对非生物和生物胁迫的保护。
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来源期刊
Current Plant Biology
Current Plant Biology Agricultural and Biological Sciences-Plant Science
CiteScore
10.90
自引率
1.90%
发文量
32
审稿时长
50 days
期刊介绍: Current Plant Biology aims to acknowledge and encourage interdisciplinary research in fundamental plant sciences with scope to address crop improvement, biodiversity, nutrition and human health. It publishes review articles, original research papers, method papers and short articles in plant research fields, such as systems biology, cell biology, genetics, epigenetics, mathematical modeling, signal transduction, plant-microbe interactions, synthetic biology, developmental biology, biochemistry, molecular biology, physiology, biotechnologies, bioinformatics and plant genomic resources.
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