Characterization of Streptomyces levis L2 with plant disease-inhibiting and growth-promoting effects
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    Abstract:

    [Objective] To study the plant disease-inhibiting and growth-promoting effects and identify the antimicrobial components of Streptomyces levis L2. [Methods] Morphological features and the phylogenetic tree based on the 16S rRNA gene sequences were employed to identify the strain L2 isolated from the rhizosphere of drought-tolerant Echinochloa crusgalli. The antimicrobial components produced by the strain were identified by chromatography and high-resolution mass spectrometry. The whole genome of the strain was sequenced by Illumina in combination with Nanopore. antiSMASH was employed to search for the biosynthetic gene clusters. [Results] Streptomyces levis L2 and its fermentation broth inhibited the growth of Gram-positive bacteria and phytopathogenic fungi, and the strain produced a large transparent zone on the CAS (chrome azurol sulphonate) plate and could produce indole-3-acetic acid (IAA). The antimicrobial components of the strain showed the m/z of 537.102 0 [M+H]+ (calcd for C27H20O12, 537.103 5, 2.2×10–6) and 523.086 3 [M+H]+ (calcd for C26H18O12, 523.087 8, 2.9×10–6), which were consistent with the exact masses of α-rubromycins, β-rubromycins and γ-rubromycins, with the errors less than parts per 5 million. Their HPLC retention time were in agreement with that of standard rubromycins. The whole genome of L2 had a length of 8.8 Mb and carried 32 biosynthetic gene clusters for secondary metabolites including rubromycins. [Conclusion] S. levis L2 exhibited excellent plant disease-inhibiting and growth-promoting properties, thus could be further developed as biocontrol agents. It produces the antimicrobial components rubromycins and its biosynthetic gene clusters contained 6 more modification genes than the previously published gene clusters for rubromycins and several genes with unknown functions.

    Reference
    [1] GLICK BR. Plant growth-promoting bacteria: mechanisms and applications[J]. Scientifica, 2012, 2012: 963401.
    [2] AMARESAN N, KUMAR K, NAIK JH, BAPATLA KG, MISHRA RK. Streptomyces in plant growth promotion[M]//New and Future Developments in Microbial Biotechnology and Bioengineering. Amsterdam: Elsevier, 2018: 125-135.
    [3] PARTE AC, SARDÀ CARBASSE J, MEIER-KOLTHOFF JP, REIMER LC, GÖKER M. List of Prokaryotic names with Standing in Nomenclature (LPSN) moves to the DSMZ[J]. International Journal of Systematic and Evolutionary Microbiology, 2020, 70(11): 5607-5612.
    [4] TANG Y, ZHANG CY, LONG QS, LEI P, GUO ZH, LIU QS. Sandaracinobacteroides saxicola sp. nov., a zeaxanthin-producing and halo-sensitive bacterium isolated from fully weathered granitic soil, and the diversity of its ARHDs[J]. Diversity, 2022, 14(10): 807.
    [5] BENNDORF R, GUO HJ, SOMMERWERK E, WEIGEL C, GARCIA-ALTARES M, MARTIN K, HU HF, KÜFNER M, de BEER ZW, POULSEN M, BEEMELMANNS C. Natural products from Actinobacteria associated with fungus-growing termites[J]. Antibiotics, 2018, 7(3): 83.
    [6] GARCÍA-FRAILE P, BENADA O, CAJTHAML T, BALDRIAN P, LLADÓ S. Terracidiphilus gabretensis gen. nov., sp. nov., an abundant and active forest soil Acidobacterium important in organic matter transformation[J]. Applied and Environmental Microbiology, 2015, 82(2): 560-569.
    [7] 蔡长平, 黄军, 曾艳, 毕世宇, 黄彬彬, 郭照辉, 刘清术. 一株辣椒内生拮抗细菌的筛选及初步鉴定[J]. 湖南农业科学, 2018(7): 1-4. CAI CP, HUANG J, ZENG Y, BI SY, HUANG BB, GUO ZH, LIU QS. Isolation and primary identification of an endophytic antagonistic bacteria from pepper[J]. Hunan Agricultural Sciences, 2018(7): 1-4(in Chinese).
    [8] YOON SH, HA SM, KWON S, LIM J, KIM Y, SEO H, CHUN J. Introducing EzBioCloud: a taxonomically united database of 16S rRNA gene sequences and whole-genome assemblies[J]. International Journal of Systematic and Evolutionary Microbiology, 2017, 67(5): 1613-1617.
    [9] KIM M, OH HS, PARK SC, CHUN J. Towards a taxonomic coherence between average nucleotide identity and 16S rRNA gene sequence similarity for species demarcation of prokaryotes[J]. International Journal of Systematic and Evolutionary Microbiology, 2014, 64(Pt 2): 346-351.
    [10] BLIN K, SHAW S, AUGUSTIJN HE, REITZ ZL, BIERMANN F, ALANJARY M, FETTER A, TERLOUW BR, METCALF WW, HELFRICH EJN, van WEZEL GP, MEDEMA MH, WEBER T. antiSMASH 7.0: new and improved predictions for detection, regulation, chemical structures and visualisation[J]. Nucleic Acids Research, 2023, 51(W1): 46-50.
    [11] TANG JT, LI YK, ZHANG LL, MU JT, JIANG YY, FU HL, ZHANG YF, CUI HF, YU XP, YE ZH. Biosynthetic pathways and functions of indole-3-acetic acid in microorganisms[J]. Microorganisms, 2023, 11(8): 2077.
    [12] SILES JA, STARKE R, MARTINOVIC T, PARENTE FERNANDES ML, ORGIAZZI A, BASTIDA F. Distribution of phosphorus cycling genes across land uses and microbial taxonomic groups based on metagenome and genome mining[J]. Soil Biology and Biochemistry, 2022, 174: 108826.
    [13] FARAMARZIAN AZIMI MARAGHEH B, FATOURACHI P, MOHAMMADI SM, VALIPOUR B, BEHTARI M, DEHNAD A, NOZAD CHAROUDEH H. Streptomyces levis ABRIINW111 inhibits SW480 cells growth by apoptosis induction[J]. Advanced Pharmaceutical Bulletin, 2018, 8(4): 675-682.
    [14] SINGH V, HAQUE S, KHARE S, TIWARI AK, KATIYAR D, BANERJEE B, KUMARI K, TRIPATHI CKM. Isolation and purification of antibacterial compound from Streptomyces levis collected from soil sample of north India[J]. PLoS One, 2018, 13(7): e0200500.
    [15] ATKINSON DJ, BRIMBLE MA. Isolation, biological activity, biosynthesis and synthetic studies towards the rubromycin family of natural products[J]. Natural Product Reports, 2015, 32(6): 811-840.
    [16] WANG XC, ELSHAHAWI SI, PONOMAREVA LV, YE Q, LIU Y, COPLEY GC, HOWER JC, HATCHER BE, KHAREL MK, van LANEN SG, SHE QB, VOSS SR, THORSON JS, SHAABAN KA. Structure determination, functional characterization, and biosynthetic implications of nybomycin metabolites from a mining reclamation site-associated Streptomyces[J]. Journal of Natural Products, 2019, 82(12): 3469-3476.
    [17] MARTIN R. Isolation and heterologous expression of Streptomyces collinus DSM 2012 genes for polyketide biosynthesis: biosynthesis of the novel polyketide antibiotic 6C-R[D]. Geneva: Doctoral Dissertation of University of Geneva, 1998.
    [18] YI LW, KONG JQ, XIONG Y, YI SR, GAN T, HUANG CS, DUAN YW, ZHU XC. Genome mining of Streptomyces sp. CB00271 as a natural high-producer of β-rubromycin and the resulting discovery of β-rubromycin acid[J]. Biotechnology and Bioengineering, 2021, 118(6): 2243-2254.
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HUANG Jun, TANG Ying, HUANG Binbin, LI Ye, ZHANG Cuiyang, GUO Zhaohui, LIU Qingshu. Characterization of Streptomyces levis L2 with plant disease-inhibiting and growth-promoting effects. [J]. Acta Microbiologica Sinica, 2024, 64(12): 4859-4868

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History
  • Received:July 17,2024
  • Online: December 07,2024
  • Published: December 04,2024
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