壳寡糖及微生物代谢产物在农业生产中的应用

杨莹, 樊丽, 杨志超, 曹鑫博, 葛菁萍

中国农学通报. 2025, 41(8): 83-89

PDF(1434 KB)
PDF(1434 KB)
中国农学通报 ›› 2025, Vol. 41 ›› Issue (8) : 83-89. DOI: 10.11924/j.issn.1000-6850.casb2024-0398
资源·环境·生态·土壤·气象

壳寡糖及微生物代谢产物在农业生产中的应用

作者信息 +

Application of COS and Microbial Metabolites in Agricultural Production

Author information +
History +

摘要

本研究综合评估了壳寡糖(Chitosan oligosaccharide, COS)的制备技术,并深入分析了COS和微生物代谢产物对植物生长、作物品质提升及病虫害管理的影响,旨在增强农业生产效率和推动环境的可持续性。通过实验研究发现,COS和微生物代谢产物在提高农业产量和维持环境稳定方面具有重要作用。针对由自然和人为活动引起的气候和生态系统变化对粮食安全构成的挑战,我们提出未来开展关于COS等有机纳米颗粒以及微生物代谢产物活性的深入研究,并强调加强发展新兴肥料研究的必要性,以期为农业生产的可持续发展提供科学依据和技术支持。

Abstract

This study comprehensively evaluated the preparation techniques of chitosan oligosaccharide (COS) and conducted an in-depth analysis of the effects of COS and microbial metabolites on plant growth, crop quality enhancement, and pest management, aiming to enhance agricultural production efficiency and promote environmental sustainability. The results revealed the importance of COS and microbial metabolites in improving agricultural yield and maintaining environmental stability. In response to the challenges posed to food security by climate and ecosystem changes caused by natural and human activities, we propose that future research should focus on the activities of organic nanoparticles such as COS and microbial metabolites, and emphasize the necessity of advancing emerging fertilizer research to provide scientific basis and technical support for the sustainable development of agricultural production.

关键词

壳寡糖 / 微生物代谢产物 / 应用 / 生物防治 / 促进植物生长发育 / 作物品质 / 病虫害管理 / 可持续发展

Key words

chitosan oligosaccharide (COS) / microbial metabolites / application / biological control / promote plant growth and development / crop quality / pest management / sustainable development

引用本文

导出引用
杨莹 , 樊丽 , 杨志超 , 曹鑫博 , 葛菁萍. 壳寡糖及微生物代谢产物在农业生产中的应用. 中国农学通报. 2025, 41(8): 83-89 https://doi.org/10.11924/j.issn.1000-6850.casb2024-0398
YANG Ying , FAN Li , YANG Zhichao , CAO Xinbo , GE Jingping. Application of COS and Microbial Metabolites in Agricultural Production. Chinese Agricultural Science Bulletin. 2025, 41(8): 83-89 https://doi.org/10.11924/j.issn.1000-6850.casb2024-0398

参考文献

[1]
ABBAS M, RIBEIRO P F, SANTOS J L. Farming system change under different climate scenarios and its impact on food security: an analytical framework to inform adaptation policy in developing countries[J]. Mitigation and adaptation strategies for global change, 2023, 28(8):43.
[2]
KASTNER T, CHAUDHARY A, GINGRICH S, et al. Global agricultural trade and land system sustainability: Implications for ecosystem carbon storage, biodiversity, and human nutrition[J]. One earth, 2021, 4(10):1425-1443.
[3]
KHAN S, HANJRA M A. Footprints of water and energy inputs in food production - Global perspectives[J]. Food policy, 2009, 34(2):130-140.
[4]
GAO X, LI C, ZHANG M, et al. Controlled release urea improved the nitrogen use efficiency, yield and quality of potato (Solanum tuberosum L.) on silt loamy soil[J]. Field crops research, 2015,181:60-68.
[5]
MOORE J A M, ABRAHAM P E, MICHENER JOSHUA K, et al. Ecosystem consequences of introducing plant growth promoting rhizobacteria to managed systems and potential legacy effects[J]. New phytologist, 2022, 234(6):1914-1918.
[6]
JIANG Y, YUE Y, WANG Z, et al. Plant biostimulant as an environmentally friendly alternative to modern agriculture[J]. Journal of agricultural and food chemistry, 2024, 72(10):5107-5121.
Ensuring the safety of crop production presents a significant challenge to humanity. Pesticides and fertilizers are commonly used to eliminate external interference and provide nutrients, enabling crops to sustain growth and defense. However, the addition of chemical substances does not meet the environmental standards required for agricultural production. Recently, natural sources such as biostimulants have been found to help plants with growth and defense. The development of biostimulants provides new solutions for agricultural product safety and has become a widely utilized tool in agricultural. The review summarizes the classification of biostimulants, including humic-based biostimulant, protein-based biostimulant, oligosaccharide-based biostimulant, metabolites-based biostimulants, inorganic substance, and microbial inoculant. This review attempts to summarize suitable alternative technology that can address the problems and analyze the current state of biostimulants, summarizes the research mechanisms, and anticipates future technological developments and market trends, which provides comprehensive information for researchers to develop biostimulants.
[7]
MUANPRASAT C, CHATSUDTHIPONG V. Chitosan oligosaccharide: Biological activities and potential therapeutic applications[J]. Pharmacology & therapeutics, 2017,170:80-97.
[8]
MUKHTAR AHMED K B, KHAN M M A, SIDDIQUI H, et al. Chitosan and its oligosaccharides, a promising option for sustainable crop production- a review[J]. Carbohydrate polymers, 2020,1:227:115331.
[9]
LIAQAT F, ELTEM R. Chitooligosaccharides and their biological activities: A comprehensive review[J]. Carbohydrate polymers, 2018,184:243-259.
[10]
TROMBOTTO S, LADAVIERE C, DELOLME F, et al. Chemical preparation and structural characterization of a homogeneous series of chitin/chitosan oligomers[J]. Biomacromolecules, 2008, 9(7):1731-1738.
The preparation of a homogeneous series of chitin/chitosan oligomers (chito-oligomers) with the same distribution of degrees of polymerization (DP) ranging from 2 to 12, but with various average degrees of N-acetylation (DA) from 0 to 90% is described. This DA-series was obtained according to a two-step chemical process involving (i) the production of a well-defined mixture of glucosamine (GlcN) oligomers obtained by acid hydrolysis of a fully N-deacetylated chitosan and after selective precipitations of the hydrolysis products, and (ii) the partial N-acetylation of the GlcN units of these oligomers from a hydro-alcoholic solution of acetic anhydride in a controlled manner. The characterization of this series of samples with different DAs by proton nuclear magnetic resonance (1H NMR) spectroscopy and matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF MS) allowed us to determine their average DA and identify the main oligomer structures constituting each mixture. Furthermore, MALDI-TOF MS was particularly helpful to study the distribution evolution of the diverse oligomers as a function of DA for the main DPs from 3 to 7. The modeling of these distributions by means of a binomial law displayed that the chemical N-acetylation of low DP GlcN oligomers, produced in a homogeneous medium, occurs randomly along the oligosaccharide chains in accordance with a statistical (Bernoullian) arrangement. In this case, the relative proportion of each chito-oligomer present in the mixture can be estimated precisely as a function of DA considering oligomers of same DP.
[11]
ZHISHEN J D S. Eeffect of reaction temperature and reaction time on the preparation of low-molecular-weight chitosan using phosphoric acid[J]. Carbohydrate polymers, 2002,49:393-396.
[12]
TISHCHENKO G, ŠIMŮNEK J, BRUS J, et al. Low-molecular-weight chitosans: Preparation and characterization[J]. Carbohydrate polymers, 2011, 86(2):1077-1081.
[13]
XIA Z, WU S, CHEN J. Preparation of water soluble chitosan by hydrolysis using hydrogen peroxide[J]. International journal of biological macromolecules, 2013,59:242-245.
[14]
MITTAL A, SINGH A, BUATONG J, et al. Chitooligosaccharide and its derivatives: potential candidates as food additives and bioactive components[J]. Foods, 2023, 12(20):3854-3882.
[15]
POPA-NITA S, LUCAS J-M, LADAVIERE C, et al. Mechanisms involved during the ultrasonically induced depolymerization of chitosan: Characterization and control[J]. Biomacromolecules, 2009, 10(5):1203-1211.
[16]
TERáN HILARES R, DOS SANTOS J G, SHIGUEMATSU N B, et al. Low-pressure homogenization of tomato juice using hydrodynamic cavitation technology: Effects on physical properties and stability of bioactive compounds[J]. Ultrasonics sonochemistry, 2019,54:192-197.
[17]
WU Y, HUANG Y, ZHOU Y, et al. Degradation of chitosan by swirling cavitation[J]. Innovative food science & emerging technologies, 2014,23:188-193.
[18]
VISHU KUMAR A. Low molecular weight chitosans: preparation with the aid of papain and characterization[J]. Biochimica et biophysica acta (BBA) - general subjects, 2004, 1670(2):137-146.
[19]
CHENG C Y, CHANG C H, WU Y J, et al. Exploration of glycosyl hydrolase family 75, a chitosanase from Aspergillus fumigatus[J]. Journal of biological chemistry, 2006, 281(6):3137-3144.
[20]
POSHINA D N, RAIK S V, POSHIN A N, et al. Accessibility of chitin and chitosan in enzymatic hydrolysis: A review[J]. Polymer degradation and stability, 2018,156:269-278.
[21]
WU S. Preparation of chitooligosaccharides from Clanis bilineata larvae skin and their antibacterial activity[J]. International journal of biological macromolecules, 2012, 51(5):1147-1150.
[22]
HAMER S N, CORD-LANDWEHR S, BIARNéS X, et al. Enzymatic production of defined chitosan oligomers with a specific pattern of acetylation using a combination of chitin oligosaccharide deacetylases[J]. Scientific reports, 2015,3:5:8716.
[23]
HEMBACH L, CORD-LANDWEHR S, MOERSCHBACHER B M. Enzymatic production of all fourteen partially acetylated chitosan tetramers using different chitin deacetylases acting in forward or reverse mode[J]. Scientific reports, 2017, 7(1):17692.
Some of the most abundant biomolecules on earth are the polysaccharides chitin and chitosan of which especially the oligomeric fractions have been extensively studied regarding their biological activities. However, most of these studies have not been able to assess the activity of a single, defined, partially acetylated chitosan oligosaccharide (paCOS). Instead, they have typically analyzed chemically produced, rather poorly characterized mixtures, at best with a single, defined degree of polymerization (DP) and a known average degree of acetylation (DA), as no pure and well-defined paCOS are currently available. We here present data on the enzymatic production of all 14 possible partially acetylated chitosan tetramers, out of which four were purified (>95%) regarding DP, DA, and pattern of acetylation (PA). We used bacterial, fungal, and viral chitin deacetylases (CDAs), either to partially deacetylate the chitin tetramer; or to partially re-N-acetylate the glucosamine tetramer. Both reactions proceeded with surprisingly strong and enzyme-specific regio-specificity. These pure and fully defined chitosans will allow to investigate the particular influence of DP, DA, and PA on the biological activities of chitosans, improving our basic understanding of their modes of action, e.g. their molecular perception by patter recognition receptors, but also increasing their usefulness in industrial applications.
[24]
CAI Q, GU Z, CHEN Y, et al. Degradation of chitosan by an electrochemical process[J]. Carbohydrate polymers, 2010, 79(3):783-785.
[25]
GU Z, CAI Q, LIU Y, et al. Electrochemical degradation of chitosan using Ti/Sb-SnO2 Electrode[J]. Journal of polymers and the environment, 2012, 21(2):479-486.
[26]
JIA X, MENG Q, ZENG H, et al. Chitosan oligosaccharide induces resistance to Tobacco mosaic virus in Arabidopsis via the salicylic acid-mediated signalling pathway[J]. Scientific reports, 2016,18:6:26144.
[27]
ZHANG H, ZHAO X, YANG J, et al. Nitric oxide production and its functional link with OIPK in tobacco defense response elicited by chitooligosaccharide[J]. Plant cell reports, 2011, 30(6):1153-1162.
Chitooligosaccharide (COS) or oligochitosan has been shown to induce tobacco defense responses which are connected with nitric oxide (NO) and OIPK (oligochitosan-induced Ser/Thr protein kinase). The aim of this study was to reveal the relationship between NO production and OIPK pathway in the defense response of tobacco elicited by COS. NO generation was investigated by epidermal strip bioassay and fluorophore microscope using fluorophore diaminofluorescein diacetate (DAF-2DA). Tobacco epidermal cells treated with COS resulted in production of NO, which was first present in chloroplast, then in nucleus, finally in the whole cell; this NO production was sensitive to NO scavenger cPTIO and the mammalian NO synthase (NOS) inhibitor L: -NAME, suggesting that NOS-like enzyme maybe involved in NO generation in tobacco epidermal cells. However, NOS and nitrate reductase (NR, EC 1.6.6.1) inhibitors reduced NO content in tobacco leaves by using NO Assay Kit, suggesting both NOS and NR were involved in NO production in tobacco leaves. Using a pharmacological approach and western blotting, we provide evidence that NO acts upstream of OIPK expression. NO scavenger, NOS inhibitor partly blocked the activation of OIPK and the activities of several defense-related enzymes induced by COS; treatment with NO donor sodium nitroprusside (SNP) induced the activation of OIPK and enhanced the defense systems. The results suggest that COS is able to induce NO generation, which results in up-regulation the activities of some defense-related enzymes through an OIPK-dependent or independent pathway.
[28]
YANG A, YU L, CHEN Z, et al. Label-free quantitative proteomic analysis of chitosan oligosaccharide-treated rice infected with southern rice black-streaked dwarf virus[J]. Viruses, 2017, 9(5):115.
[29]
COBOS R, MATEOS R M, ÁLVAREZ-PéREZ J M, et al. Effectiveness of natural antifungal compounds in controlling infection by grapevine trunk disease pathogens through pruning wounds[J]. Applied and environmental microbiology, 2015, 81(18):6474-6483.
Grapevine trunk fungal pathogens, such as Diplodia seriata and Phaeomoniella chlamydospora, can infect plants through pruning wounds. They cause grapevine trunk diseases and are involved in grapevine decline. Accordingly, the protection of pruning wounds is crucial for the management of grapevine trunk diseases. The efficacy of different natural antifungals in inhibiting the growth of several fungi causing grapevine trunk diseases was evaluated in vitro. The fungi showing greater in vitro efficacy were tested on autoclaved grape wood assays against D. seriata and P. chlamydospora. Based on results from these assays, chitosan oligosaccharide, vanillin, and garlic extract were selected for further evaluation on pruning wounds inoculated with D. seriata and P. chlamydospora in field trials. A significant decrease in plant mortality was observed after 2 years of growth in the plants treated with the different natural antifungals compared to the mortality rate observed in infected plants that were not treated with antifungals. Also, the infection rate for the inoculated pathogens was significantly reduced in plants treated with the selected natural antifungals. Therefore, natural antifungals represent a promising alternative for disease control and could provide significant economic benefits for the grape-growing industry. Copyright © 2015, American Society for Microbiology. All Rights Reserved.
[30]
KIM S W, PARK J K, LEE C H, et al. Comparison of the antimicrobial properties of chitosan oligosaccharides (COS) and EDTA against Fusarium fujikuroi causing rice bakanae disease[J]. Current microbiology, 2016, 72(4):496-502.
[31]
SUN G, YANG Q, ZHANG A, et al. Synergistic effect of the combined bio-fungicides ε-poly- l -lysine and chitooligosaccharide in controlling grey mould ( Botrytis cinerea ) in tomatoes[J]. International journal of food microbiology, 2018,276:46-53.
[32]
YIN H, FRETTé X C, CHRISTENSEN L P, et al. Chitosan oligosaccharides promote the content of polyphenols in greek oregano (Origanum vulgare ssp. hirtum)[J]. Journal of agricultural and food chemistry, 2011, 60(1):136-143.
[33]
GUO W, YIN H, YE Z, et al. A comparison study on the interactions of two oligosaccharides with tobacco cells by time-resolved fluorometric method[J]. Carbohydrate polymers, 2012, 90(1):491-495.
The interactions of tobacco cells with two oceanic oligosaccharides, chitosan oligosaccharide (COS) and alginate derived oligosaccharide (AOS) were investigated and compared by time-resolved fluorometric method using two Eu(3+) complexes as luminescence probes. The binding processes of two oligosaccharides and tobacco leaf cells (epidermal and stomatal guard cells) were characterized by the luminescence imaging method based on the reaction of tobacco cells with oligosaccharide (COS or AOS) conjugated to a highly fluorescent Eu(3+) complex. In addition, the concentration changes of indole-3-acetic acid (IAA) and IAA-related peroxidase produced in the cells during the interaction of oligosaccharides (COS or AOS) and tobacco cells were also determined. The results indicate that the bioactivity of COS, with faster binding rate to the tobacco cells and stronger effect on the IAA generation in the cells, is remarkably higher than that of AOS. The comparison study on bioactivities of the two oligosaccharides reveals the relationship between structures and bioactivities of oligosaccharide, and suggests that COS should be more favorable to be used as a promotion reagent of plant growth in agriculture field. Copyright © 2012 Elsevier Ltd. All rights reserved.
[34]
GOUGH C, CULLIMORE J. Lipo-chitooligosaccharide signaling in edosymbiotic plant-microbe interactions[J]. Molecular plant-microbe interactions, 2011, 24(8):867-878.
[35]
TANAKA K, CHO S-H, LEE H, et al. Effect of lipo-chitooligosaccharide on early growth of C4 grass seedlings[J]. Journal of experimental botany, 2015, 66(19):5727-5738.
Although lipo-chitooligosaccharides (LCOs) are important signal molecules for plant-symbiont interactions, a number of reports suggest that LCOs can directly impact plant growth and development, separate from any role in plant symbioses. In order to investigate this more closely, maize and Setaria seedlings were treated with LCO and their growth was evaluated. The data indicate that LCO treatment significantly enhanced root growth. RNA-seq transcriptomic analysis of LCO-treated maize roots identified a number of genes whose expression was significantly affected by the treatment. Among these genes, some LCO-up-regulated genes are likely involved in root growth promotion. Interestingly, some stress-related genes were down-regulated after LCO treatment, which might indicate reallocation of resources from defense responses to plant growth. The promoter activity of several LCO-up-regulated genes using a β-glucuronidase reporter system was further analysed. The results showed that the promoters were activated by LCO treatment. The data indicate that LCO can directly impact maize root growth and gene expression. © The Author 2015. Published by Oxford University Press on behalf of the Society for Experimental Biology.
[36]
HE Y, BOSE S, WANG W, et al. Pre-harvest treatment of chitosan oligosaccharides improved strawberry fruit quality[J]. International journal of molecular sciences, 2018, 19(8):2194.
[37]
GUO X, YU Z, ZHANG M, et al. Enhancing the production of phenolic compounds during barley germination by using chitooligosaccharides to improve the antioxidant capacity of malt[J]. Biotechnology letters, 2018, 40(9-10):1335-1341.
To enhance the production of phenolic compounds during barley germination using chitooligosaccharide as an elicitor to improve the antioxidant capacity of malt.When used as an elicitor for barley germination, chitooligosaccharide with a molecular weight of 3 kDa, added at 10 mg/kg barley kernels during the first steeping cycle, led to the maximum production of phenolic compounds. Compared with the control with no chitooligosaccharide added to the steeping water, the total phenolic content was increased by 54.8%. Increases in the total phenolic content of the barley malt occurred when chitooligosaccharide was applied during the first or both the first and the second steeping cycles. Thus the antioxidant capacity of barley malt was increased significantly by adding chitooligosaccharide during the steeping process.Applying chitooligosaccharides during the steeping process increased the content of phenolic compounds thus improving the antioxidant capacity of the barley malt.
[38]
LAN W, WANG W, YU Z, et al. Enhanced germination of barley (Hordeum vulgare L.) using chitooligosaccharide as an elicitor in seed priming to improve malt quality[J]. Biotechnology letters, 2016, 38(11):1935-1940.
[39]
ABDEL LATEF A A H, ABU ALHMAD M F, KORDROSTAMI M, et al. Inoculation with Azospirillum lipoferum or Azotobacter chroococcum reinforces maize growth by improving physiological activities under saline conditions[J]. Journal of plant growth regulation, 2020, 39(3):1293-1306.
[40]
OZIMEK E, JAROSZUK-ŚCISEŁ J, BOHACZ J, et al. Synthesis of indoleacetic ccid, gibberellic acid and ACC-deaminase by Mortierella strains promote winter wheat seedlings growth under different conditions[J]. International journal of molecular sciences, 2018, 19(10):3218.
[41]
PARAĐIKOVIĆ N, TEKLIĆ T, ZELJKOVIĆ S, et al. Biostimulants research in some horticultural plant species—a review[J]. Food and energy security, 2018, 8(2):e00162.
[42]
KOUR D, RANA K L, YADAV A N, et al. Microbial biofertilizers: bioresources and eco-friendly technologies for agricultural and environmental sustainability[J]. Biocatalysis and agricultural biotechnology, 2020,23:101487.
[43]
RADHAKRISHNAN R, HASHEM A, ABD_ALLAH E F. Bacillus: a biological tool for crop improvement through bio-molecular changes in adverse environments[J]. Frontiers in physiology, 2017,8:667.
[44]
DÍAZ-RUEDA P, MORALES DE LOS RÍOS L, ROMERO L C, et al. Old poisons, new signaling molecules: the case of hydrogen cyanide[J]. Journal of experimental botany, 2023, 74(19):6040-6051.
[45]
LLORENTE B E, ALASIA M A, LARRABURU E E. Biofertilization with Azospirillum brasilense improves in vitro culture of Handroanthus ochraceus, a forestry, ornamental and medicinal plant[J]. New biotechnology, 2016, 33(1):32-40.
[46]
ORTIZ-CASTRO R, CAMPOS-GARCíA J, LóPEZ-BUCIO J. Pseudomonas putida and Pseudomonas fluorescens influence Arabidopsis root system architecture through an auxin response mediated by bioactive cyclodipeptides[J]. Journal of plant growth regulation, 2019, 39(1):254-265.
[47]
HELLEQUIN E, MONARD C, CHORIN M, et al. Responses of active soil microorganisms facing to a soil biostimulant input compared to plant legacy effects[J]. Scientific reports, 2020, 10(1):13727.
Agriculture is changing to rely on agroecological practices that take into account biodiversity, and the ecological processes occurring in soils. The use of agricultural biostimulants has emerged as a valid alternative to chemicals to indirectly sustain plant growth and productivity. Certain BS have been shown to select and stimulate plant beneficial soil microorganisms. However, there is a lack of knowledge on the effects and way of action of the biostimulants operating on soil functioning as well as on the extent and dynamic of these effects. In this study we aimed to decipher the way of action of a seaweed and amino-acids based biostimulant intended to be applied on soil crop residues to increase their microbial mineralization and the further release of nutrients. By setting-up a two-phase experiment (soil plant-growing and soil incubation), our objectives were to (1) determine the effects of the soil biostimulant over time on the active soil bacteria and fungi and the consequences on the organic carbon mineralization in bare soils, and (2) assess the biostimulant effects on soil microorganisms relatively to plant legacy effects in planted soils. We demonstrated that the soil biostimulant had a delayed effect on the active soil microorganisms and activated both plant growth promoting bacteria and saprophytes microorganisms at the medium-term of 49 days. However, the changes in the abundances of active microbial decomposers were not associated to a higher mineralization rate of organic carbon derived from soil and/or litter. The present study assessed the biostimulant beneficial effect on active soil microbial communities as similar as or even higher than the legacy effects of either A. thaliana or T. aestivum plants. We specifically showed that the biostimulant increased the active fungal richness to a higher extent than observed in soils that previously grew the two plants tested.
[48]
CHATTOPADHYAY A, PUROHIT J, TIWARI K K, et al. Targeting transcription factors for plant disease resistance: shifting paradigm[J]. Current science, 2019, 117(10):1598-1607.
[49]
TANG C, XU Q, ZHAO M, et al. Understanding the lifestyles and pathogenicity mechanisms of obligate biotrophic fungi in wheat: the emerging genomics era[J]. The crop journal, 2018, 6(1):60-67.
[50]
TELI B, PUROHIT J, RASHID M M, et al. Omics insight on Fusarium Head Blight of wheat for translational research perspective[J]. Current genomics, 2020, 21(6):411-428.
[51]
SUSIČ N, JANEŽIČ S, RUPNIK M, et al. Whole genome sequencing and comparative genomics of two nematicidal Bacillus strains reveals a wide range of possible virulence factors[J]. G3 genes genomes genetics, 2020, 10(3):881-890.
[52]
MARCHE M G, CAMIOLO S, PORCEDDU A, et al. Survey of Brevibacillus laterosporus insecticidal protein genes and virulence factors[J]. Journal of invertebrate pathology, 2018,155:38-43.
[53]
BLAINSKI J M L, DA ROCHA NETO A C, SCHIMIDT E C, et al. Exopolysaccharides from Lactobacillus plantarum induce biochemical and physiological alterations in tomato plant against bacterial spot[J]. Applied microbiology and biotechnology, 2018, 102(11):4741-4753.
[54]
BENEDUZI A, AMBROSINI A, PASSAGLIA L M P. Plant growth-promoting rhizobacteria (PGPR): their potential as antagonists and biocontrol agents[J]. Genetics and molecular biology, 2012, 35(4):1044-1051.
[55]
LU X, LIU S-F, YUE L, et al. Epsc involved in the encoding of exopolysaccharides produced by Bacillus amyloliquefaciens FZB42 act to boost the drought tolerance of Arabidopsis thaliana[J]. International journal of molecular sciences, 2018, 19(12):3795.
[56]
O'BRIEN S, HODGSON D J, BUCKLING A. Social evolution of toxic metal bioremediation in Pseudomonas aeruginosa[J]. Proceedings of the royal society b-biological sciences, 2014, 281(1787):20240858.
[57]
WANG Q, XIONG D, ZHAO P, et al. Effect of applying an arsenic-resistant and plant growth-promoting rhizobacterium to enhance soil arsenic phytoremediation by Populus deltoides LH05-17[J]. Journal of applied microbiology, 2011, 111(5):1065-1074.
[58]
SULTANA S, ALAM S, KARIM M M. Screening of siderophore-producing salt-tolerant rhizobacteria suitable for supporting plant growth in saline soils with iron limitation[J]. Journal of agriculture and food research, 2021,4:100150.
[59]
GAMALERO E, GLICK B R. Bacterial modulation of plant ethylene levels[J]. Plant physiology, 2015, 169(1):13-22.
A focus on the mechanisms by which ACC deaminase-containing bacteria facilitate plant growth.Bacteria that produce the enzyme 1-aminocyclopropane-1-carboxylate (ACC) deaminase, when present either on the surface of plant roots (rhizospheric) or within plant tissues (endophytic), play an active role in modulating ethylene levels in plants. This enzyme activity facilitates plant growth especially in the presence of various environmental stresses. Thus, plant growth-promoting bacteria that express ACC deaminase activity protect plants from growth inhibition by flooding and anoxia, drought, high salt, the presence of fungal and bacterial pathogens, nematodes, and the presence of metals and organic contaminants. Bacteria that express ACC deaminase activity also decrease the rate of flower wilting, promote the rooting of cuttings, and facilitate the nodulation of legumes. Here, the mechanisms behind bacterial ACC deaminase facilitation of plant growth and development are discussed, and numerous examples of the use of bacteria with this activity are summarized. © 2015 American Society of Plant Biologists. All Rights Reserved.
[60]
VISWANATHAN V K, RAJARAM MANOHARAN S R, SUBRAMANIAN S, et al. Nanotechnology in spine surgery: a current update and critical review of the literature[J]. World neurosurgery, 2019,123:142-155.
[61]
BUEHLER M J, YUNG Y C. Deformation and failure of protein materials in physiologically extreme conditions and disease[J]. Nature materials, 2009, 8(3):175-188.
Biological protein materials feature hierarchical structures that make up a diverse range of physiological materials. The analysis of protein materials is an emerging field that uses the relationships between biological structures, processes and properties to probe deformation and failure phenomena at the molecular and microscopic level. Here we discuss how advanced experimental, computational and theoretical methods can be used to assess structure-process-property relations and to monitor and predict mechanisms associated with failure of protein materials. Case studies are presented to examine failure phenomena in the progression of disease. From this materials science perspective, a de novo basis for understanding biological processes can be used to develop new approaches for treating medical disorders. We highlight opportunities to use knowledge gained from the integration of multiple scales with physical, biological and chemical concepts for potential applications in materials design and nanotechnology.
[62]
SABERI-RISE R, MORADI-POUR M. The effect of Bacillus subtilis Vru1 encapsulated in alginate- bentonite coating enriched with titanium nanoparticles against Rhizoctonia solani on bean[J]. International journal of biological macromolecules, 2020,152:1089-1097.
[63]
ZAHRA Z, HABIB Z, HYUN H, et al. Overview on recent developments in the design, application, and impacts of nanofertilizers in agriculture[J]. Sustainability, 2022, 14(15):9397.
[64]
AKHTAR N, ILYAS N. Role of nanosilicab to boost the activities of metabolites in Triticum aestivum facing drought stress[J]. Plant and soil, 2022, 477(1-2):99-115.
[65]
ELIASPOUR S, SEYED SHARIFI R, SHIRKHANI A, et al. Effects of biofertilizers and iron nano-oxide on maize yield and physiological properties under optimal irrigation and drought stress conditions[J]. Food science & nutrition, 2020, 8(11):5985-5998.
[66]
ZAIM N S H B H, TAN H L, RAHMAN S M A, et al. Recent advances in seed coating treatment using nanoparticles and nanofibers for enhanced seed germination and protection[J]. Journal of plant growth regulation, 2023, 42(12):7374-7402.

基金

黑龙江省高校基本业务经费“群体感应介导下重组根圈细菌菌群对土壤磷养分循环的调控机制”(2023-KYYWF-1448)
黑龙江省生态环境厅生态环境保护科研项目“人工重组细菌菌群对黑土磷障碍的解控机制”(HST20TR004)
黑龙江省自然科学基金联合培育项目“群体感应对寒地黑土遗留有机磷的矿化及迁移驱动机制研究”(PL2024D015)
PDF(1434 KB)

47

Accesses

0

Citation

Detail

段落导航
相关文章

/