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Plant growth-promoting rhizobacteria used in South Korea
Applied Biological Chemistry volume 61, pages 709–716 (2018)
Abstract
Many bacteria found in the rhizosphere provide contribution for the host plant’s growth and protection that are known as plant growth-promoting rhizobacteria (PGPR). Plant–microbe interactions in the rhizosphere are important factors in determining the health of plants. Research for commercialization of these PGPR as an alternative to the use of chemical fertilizers for a more environmentally friendly treatment is continuously being improved. In this review, we discuss the essential traits that rhizobacteria must possess for them to be considered PGPR and report the bacterial species that exhibit these essential plant growth-promoting activities and which are approved for use by the South Korean regulations.
Introduction
One of the great challenges currently under consideration is to developing environmentally wide-ranging and sustainable crop production methods. Crop production must be increased to provide food for the increasing population. Although the use of chemical fertilizers is a viable option, there are health risks associated when their improper use and these agents can cause environmental destruction. Plant biotechnology has provided insight and aided the development of new crops to overcome complications caused by abiotic stresses (soil salinization and sodification, drought, soil pH, and temperature) and biotic factors such as pathogenicity by other living organisms, including bacteria, viruses, fungi, and parasites [1, 2].
In plant–microbe interactions, which have been widely examined, the host plant and bacteria present along the rhizosphere exhibit intimate interactions. These interactions promote host plant growth and pathogen suppression. The rhizosphere is a well-characterized ecological niche affected by root exudates [3]. Bacteria with direct and indirect positive effects on the growth and health of the plant are known as plant growth-promoting rhizobacteria (PGPR). In this review, we describe various important properties required by bacterial species to be considered PGPR and report various bacterial species exhibiting PGP qualities in South Korea.
Phytohormone production
Most distinguished phytohormones are consisted of cytokinins, auxins, gibberellins, ethylene, and abscisic acid, and PGPR show potential for the production of these hormones. These phytohormones can facilitate processes such as plant cell enlargement, division, and extension of symbiotic and non-symbiotic roots [1, 4, 5]. Furthermore, plant-associated bacteria may influence the hormonal balance of a plant.
Indole acetic acid (IAA), also known as auxin, governs different stages of plant growth and development, namely cell division, cell elongation, and tissue differentiation, and assists in apical dominance. IAA produced by rhizobacteria affects the root system through the increase of weight and size, the number of branches, and the surface area in contact with the soil.
Similarly, plant responses to cytokinin application include enhanced cell division, enhanced root development, enhanced root hair formation, inhibited root elongation, shoot initiation, and other physiological responses. Gibberellins, in contrast, are a group of phytohormones that affects developmental strategies in higher plants and include stem elongation, seed germination, flowering, and fruit setting [6, 7].
Ethylene synthesis inhibition
Ethylene is another growth regulator that affects physiological processes in plants. It is related primarily to the plant’s growth and defense systems which are triggered by stress responses. Factors such as light, temperature, salinity, pathogen attacks, and nutritional status alter ethylene levels. Moreover, ethylene also facilitates additional processes not related to stress such as ripening, root elongation, and seed development. As ethylene levels decrease, root system growth increases, as described above. Degradation of 1-aminocyclopropane-1-carboxylic acid (ACC), a direct precursor of ethylene, creates a concentration gradient that favors its exudation. Maintaining a balance between the ethylene and auxin is important since the two are related growth regulators, some effects attributed to auxin-producing bacteria result from ACC degradation [1, 8].
Free nitrogen fixation
Nitrogen is a key component in the synthesis of cellular enzymes, proteins, chlorophyll, DNA, and RNA, and, as a result, it is important in plant growth. Bacterial strains capable of nitrogen fixation are divided into two categories: root/legume-associated symbiotic bacteria and free nitrogen-fixing bacteria. The former specifically infect the roots to produce nodules, while the latter are non-specific and can form symbiotic relationships with other plants and organisms [1, 9].
Phosphate solubilization
Phosphorus is the second most important mineral nutrient after nitrogen limiting plant growth. Although soils contain a high concentration of total phosphorus, the amount available for plant uptake is limited because P is in an insoluble form. Bacteria present in the rhizosphere can solubilize phosphate through different mechanisms. The most common method of solubilizing phosphorus is by secreting organic acids that act as chelators. Solubilization of P in the rhizosphere is the most common mode of action that increases the availability of nutrients for host plant uptake [10].
Production of siderophore
Another essential plant nutrient is iron. Iron serves as a cofactor for numerous enzymes that are important in physiological processes such as photosynthesis, nitrogen fixation, and respiration. Similar to phosphorus, iron is abundant in the soil but is not available for plant uptake because Fe3+ predominates and reacts to form insoluble hydroxides. In a similar manner to solubilizing phosphates, bacteria present in the rhizosphere release organic compounds for chelation. A different strategy involves absorbing the iron-organic compound complex, where the iron is reduced in the plant and directly assimilated [11].
Enzyme synthesis that hydrolyzes fungal cell walls
PGPR may be applicable in agriculture for the biocontrol of plant pathogens. Production of cell wall-degrading enzymes plays a very important role in controlling pathogens. Cell wall-degrading enzymes including chitinase, β-1,3-glucanase, cellulase, and protease that are secreted by PGPR directly inhibit the hyphal growth of fungal pathogens through the degradation of their cell which may be an alternative method for replacing chemical fungicides [2, 10, 12].
PGPR species in South Korea
South Korea is one of the top countries leading research and development for biotechnology. Development of PGPR is one focus of this field. The South Korean government approved the use of 108 total species of bacteria, yeast, and fungi as fertilizers and some species as feeds. However, there was some misunderstanding because of changes in taxonomy and some isolates were found to be the same species. In the present study, only 51 bacterial species have been identified to have strains included in the Korean Agricultural Culture Collection (KACC). Among these, 40 were found to have PGP activities in previous studies (Table 1), while the 11 species require further examination. Additional research is needed to evaluate the PGP characteristics of these 11 species (Table 2).
Conclusion
The PGP activities of rhizosphere bacteria show great promise for applications in sustainable and ecofriendly agriculture. PGPR not only promote growth by providing nutrients but are also useful as biocontrol agents to protect plants from pathogens. While the fundamentals of how PGPR promote growth are well known, there is still much more to learn about the mechanisms underlying plant–microbe interactions for commercial production for the microbes as an alternative to chemical fertilizers.
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Acknowledgments
This work was carried out with the support of “Cooperative Research Program for Agriculture Science and Technology Development (Project No. PJ013383)” Rural Development Administration, Republic of Korea.
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Ibal, J.C., Jung, B.K., Park, C.E. et al. Plant growth-promoting rhizobacteria used in South Korea. Appl Biol Chem 61, 709–716 (2018). https://doi.org/10.1007/s13765-018-0406-0
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DOI: https://doi.org/10.1007/s13765-018-0406-0