A Salt-Tolerant Streptomyces paradoxus D2-8 from Rhizosphere Soil of Phragmites communis Augments Soybean Tolerance to Soda Saline-Alkali Stress

Abulfaraj AA, Jalal RS. Use of plant growth-promoting bacteria to enhance salinity stress in soybean (Glycine max L.) plants. Saudi J Biol Sci. 2021 Jul;28(7):3823–3834. https://doi.org/10.1016/j.sjbs.2021.03.053 AbulfarajAA JalalRS Use of plant growth-promoting bacteria to enhance salinity stress in soybean (Glycine max L.) plants Saudi J Biol Sci 2021 Jul 28 7 3823 3834 https://doi.org/10.1016/j.sjbs.2021.03.053 10.1016/j.sjbs.2021.03.053 Search in Google Scholar

Berg G, Marten P, Minkwitz A, Brückner S. Efficient biological control of plant fungal diseases by Streptomyces sp. DSMZ 12424. J Plant Dis Protect. 2001 Jan;108(1):1–10. BergG MartenP MinkwitzA BrücknerS Efficient biological control of plant fungal diseases by Streptomyces sp. DSMZ 12424 J Plant Dis Protect 2001 Jan 108 1 1 10 Search in Google Scholar

Bhatti AA, Haq S, Bhat RA. Actinomycetes benefaction role in soil and plant health. Microb Pathog. 2017 Oct;111:458–467. https://doi.org/10.1016/j.micpath.2017.09.036 BhattiAA HaqS BhatRA Actinomycetes benefaction role in soil and plant health Microb Pathog 2017 Oct 111 458 467 https://doi.org/10.1016/j.micpath.2017.09.036 10.1016/j.micpath.2017.09.036 Search in Google Scholar

Chatterton S, Punja ZK. Factors influencing colonization of cucumber roots by Clonostachys rosea f. catenulata, a biological disease control agent. Biocontrol Sci Technol. 2010;20(1):37–55. https://doi.org/10.1080/09583150903350253 ChattertonS PunjaZK Factors influencing colonization of cucumber roots by Clonostachys rosea f. catenulata, a biological disease control agent Biocontrol Sci Technol 2010 20 1 37 55 https://doi.org/10.1080/09583150903350253 10.1080/09583150903350253 Search in Google Scholar

Costa-Gutierrez SB, Lami MJ, Santo MCC, Zenoff AM, Vincent PA, Molina-Henares MA, Espinosa-Urgel M, de Cristóbal RE. Plant growth promotion by Pseudomonas putida KT2440 under saline stress: role of eptA. Appl Microbiol Biotechnol. 2020 May;104(10): 4577–4592. https://doi.org/10.1007/s00253-020-10516-z Costa-GutierrezSB LamiMJ SantoMCC ZenoffAM VincentPA Molina-HenaresMA Espinosa-UrgelM de CristóbalRE Plant growth promotion by Pseudomonas putida KT2440 under saline stress: role of eptA Appl Microbiol Biotechnol 2020 May 104 10 4577 4592 https://doi.org/10.1007/s00253-020-10516-z 10.1007/s00253-020-10516-z Search in Google Scholar

Gang S, Sharma S, Saraf M, Buck M, Schumacher J. Analysis of indole-3-acetic acid (IAA) production in Klebsiella by LC-MS/MS and the Salkowski method. Bio Protoc. 2019 May 5;9(9):e3230. https://doi.org/10.21769/BioProtoc.3230 GangS SharmaS SarafM BuckM SchumacherJ Analysis of indole-3-acetic acid (IAA) production in Klebsiella by LC-MS/MS and the Salkowski method Bio Protoc 2019 May 5 9 9 e3230 https://doi.org/10.21769/BioProtoc.3230 10.21769/BioProtoc.3230 Search in Google Scholar

Guillot A, Obis D, Mistou MY. Fatty acid membrane composition and activation of glycine-betaine transport in Lactococcus lactis subjected to osmotic stress. Int J Food Microbiol. 2000 Apr 10;55(1–3): 47–51. https://doi.org/10.1016/s0168-1605(00)00193-8 GuillotA ObisD MistouMY Fatty acid membrane composition and activation of glycine-betaine transport in Lactococcus lactis subjected to osmotic stress Int J Food Microbiol 2000 Apr 10 55 1–3 47 51 https://doi.org/10.1016/s0168-1605(00)00193-8 10.1016/S0168-1605(00)00193-8 Search in Google Scholar

Han D, Wang L, Luo Y. Isolation, identification, and the growth promoting effects of two antagonistic actinomycete strains from the rhizosphere of Mikania micrantha Kunth. Microbiol Res. 2018 Mar; 208:1–11. https://doi.org/10.1016/j.micres.2018.01.003 HanD WangL LuoY Isolation, identification, and the growth promoting effects of two antagonistic actinomycete strains from the rhizosphere of Mikania micrantha Kunth Microbiol Res 2018 Mar 208 1 11 https://doi.org/10.1016/j.micres.2018.01.003 10.1016/j.micres.2018.01.00329551207 Search in Google Scholar

Han L, Zhang H, Xu Y, Li Y, Zhou J. Biological characteristics and salt-tolerant plant growth-promoting effects of an ACC deaminase-producing Burkholderia pyrrocinia strain isolated from the tea rhizosphere. Arch Microbiol. 2021 Jul; 203(5): 2279–2290. http://doi.org/10.1007/s00203-021-02204-x. HanL ZhangH XuY LiY ZhouJ Biological characteristics and salt-tolerant plant growth-promoting effects of an ACC deaminase-producing Burkholderia pyrrocinia strain isolated from the tea rhizosphere Arch Microbiol 2021 Jul 203 5 2279 2290 http://doi.org/10.1007/s00203-021-02204-x. 10.1007/s00203-021-02204-x33644819 Search in Google Scholar

He C, Zheng L, Ding J, Gao W, Chi W, Ding Y. Complete genome sequence of an N-acyl homoserine lactone producer, Breoghania sp. strain L-A4, isolated from rhizosphere of Phragmites australis in a coastal wetland. Microbiol Resour Announc. 2019 Jan 31;8(5): e01539-18. https://doi.org/10.1128/MRA.01539-18 HeC ZhengL DingJ GaoW ChiW DingY Complete genome sequence of an N-acyl homoserine lactone producer, Breoghania sp. strain L-A4, isolated from rhizosphere of Phragmites australis in a coastal wetland Microbiol Resour Announc 2019 Jan 31 8 5 e01539-18 https://doi.org/10.1128/MRA.01539-18 10.1128/MRA.01539-18635764030714034 Search in Google Scholar

Huang LH, Liang ZW, Suarez DL, Wang ZC, Wang MM, Yang HY, Liu M. Impact of cultivation year, nitrogen fertilization rate and irrigation water quality on soil salinity and soil nitrogen in saline-sodic paddy fields in Northeast China. J Agric Sci. 2016;154(04):632–646. https://doi.org/10.1017/S002185961500057X HuangLH LiangZW SuarezDL WangZC WangMM YangHY LiuM Impact of cultivation year, nitrogen fertilization rate and irrigation water quality on soil salinity and soil nitrogen in saline-sodic paddy fields in Northeast China J Agric Sci 2016 154 04 632 646 https://doi.org/10.1017/S002185961500057X 10.1017/S002185961500057X Search in Google Scholar

Jiang Y, Cao YR, Wiese J, Tang SK, Xu LH, Imhoff JF, Jiang CL. Streptomyces sparsus sp. nov., isolated from a saline and alkaline soil. Int J Syst Evol Microbiol. 2011 Jul;61(7):1601–1605. https://doi.org/10.1099/ijs.0.020669-0 JiangY CaoYR WieseJ TangSK XuLH ImhoffJF JiangCL Streptomyces sparsus sp. nov., isolated from a saline and alkaline soil Int J Syst Evol Microbiol 2011 Jul 61 7 1601 1605 https://doi.org/10.1099/ijs.0.020669-0 10.1099/ijs.0.020669-020693361 Search in Google Scholar

Khan MA, Asaf S, Khan AL, Jan R, Kang SM, Kim KM, Lee IJ. Rhizobacteria AK1 remediates the toxic effects of salinity stress via regulation of endogenous phytohormones and gene expression in soybean. Biochem J. 2019 Aug 30;476(16):2393–2409. https://doi.org/10.1042/BCJ20190435 KhanMA AsafS KhanAL JanR KangSM KimKM LeeIJ Rhizobacteria AK1 remediates the toxic effects of salinity stress via regulation of endogenous phytohormones and gene expression in soybean Biochem J 2019 Aug 30 476 16 2393 2409 https://doi.org/10.1042/BCJ20190435 10.1042/BCJ2019043531375565 Search in Google Scholar

Killham K, Firestone MK. Salt stress control of intracellular solutes in streptomycetes indigenous to saline soils. Appl Environ Microbiol. 1984 Feb;47(2):301–306. https://doi.org/10.1128/aem.47.2.301-306.1984 KillhamK FirestoneMK Salt stress control of intracellular solutes in streptomycetes indigenous to saline soils Appl Environ Microbiol 1984 Feb 47 2 301 306 https://doi.org/10.1128/aem.47.2.301-306.1984 10.1128/aem.47.2.301-306.198423966416346472 Search in Google Scholar

Lahdenperä ML, Simon E, Uoti J. Mycostop – A novel biofungicide based on Streptomyces bacteria. In: Beemster ABR, Bollen GJ, Gerlagh M, Ruissen MA, Schippers B, Tempel A, editors. Developments in agricultural and managed forest ecology. Amsterdam (The Netherlands): Elsevier; 1991(23), p. 258–263. https://doi.org/10.1016/B978-0-444-88728-3.50048-2 LahdenperäML SimonE UotiJ Mycostop – A novel biofungicide based on Streptomyces bacteria In: BeemsterABR BollenGJ GerlaghM RuissenMA SchippersB TempelA editors. Developments in agricultural and managed forest ecology Amsterdam (The Netherlands) Elsevier 1991 (23), 258 263 https://doi.org/10.1016/B978-0-444-88728-3.50048-2 10.1016/B978-0-444-88728-3.50048-2 Search in Google Scholar

Liu D, Yan R, Fu Y, Wang X, Zhang J, Xiang W. Antifungal, plant growth-promoting, and genomic properties of an endophytic actinobacterium Streptomyces sp. NEAU-S7GS2. Front Microbiol. 2019 Sep 10;10:2077. https://doi.org/10.3389/fmicb.2019.02077 LiuD YanR FuY WangX ZhangJ XiangW Antifungal, plant growth-promoting, and genomic properties of an endophytic actinobacterium Streptomyces sp. NEAU-S7GS2 Front Microbiol 2019 Sep 10 10 2077 https://doi.org/10.3389/fmicb.2019.02077 10.3389/fmicb.2019.02077674691831551997 Search in Google Scholar

Minuto A, Spadaro D, Garibaldi A, Gullino ML. Control of soil-borne pathogens of tomato using a commercial formulation of Streptomyces griseoviridis and solarization. Crop Prot. 2006;25(5):468–475. https://doi.org/10.1016/j.cropro.2005.08.001 MinutoA SpadaroD GaribaldiA GullinoML Control of soil-borne pathogens of tomato using a commercial formulation of Streptomyces griseoviridis and solarization Crop Prot 2006 25 5 468 475 https://doi.org/10.1016/j.cropro.2005.08.001 10.1016/j.cropro.2005.08.001 Search in Google Scholar

Newitt JT, Prudence SMM, Hutchings MI, Worsley SF. Biocontrol of cereal crop diseases using Streptomycetes. Pathogens. 2019 Jun 13; 8(2):78. https://doi.org/10.3390/pathogens8020078 NewittJT PrudenceSMM HutchingsMI WorsleySF Biocontrol of cereal crop diseases using Streptomycetes Pathogens 2019 Jun 13 8 2 78 https://doi.org/10.3390/pathogens8020078 10.3390/pathogens8020078663030431200493 Search in Google Scholar

Panda AK, Bisht SS, DeMondal S, Senthil Kumar N, Gurusubramanian G, Panigrahi AK. Brevibacillus as a biological tool: a short review. Antonie Van Leeuwenhoek. 2014 Apr;105(4):623–639. https://doi.org/10.1007/s10482-013-0099-7 PandaAK BishtSS DeMondalS Senthil KumarN GurusubramanianG PanigrahiAK Brevibacillus as a biological tool: a short review Antonie Van Leeuwenhoek 2014 Apr 105 4 623 639 https://doi.org/10.1007/s10482-013-0099-7 10.1007/s10482-013-0099-724563152 Search in Google Scholar

Pereira SI, Pires C, Henriques I, Correia A, Magan N, Castro PM. Assessment of rhizospheric culturable bacteria of Phragmites australis and Juncus effusus from polluted sites. J Basic Microbiol. 2015 Oct; 55(10):1179–1190. https://doi.org/10.1002/jobm.201500010 PereiraSI PiresC HenriquesI CorreiaA MaganN CastroPM Assessment of rhizospheric culturable bacteria of Phragmites australis and Juncus effusus from polluted sites J Basic Microbiol 2015 Oct 55 10 1179 1190 https://doi.org/10.1002/jobm.201500010 10.1002/jobm.20150001026059184 Search in Google Scholar

Phang TH, Shao G, Lam HM. Salt tolerance in soybean. J Integr Plant Biol. 2008 Oct;50(10):1196–1212. https://doi.org/10.1111/j.1744-7909.2008.00760.x PhangTH ShaoG LamHM Salt tolerance in soybean J Integr Plant Biol 2008 Oct 50 10 1196 1212 https://doi.org/10.1111/j.1744-7909.2008.00760.x 10.1111/j.1744-7909.2008.00760.x19017107 Search in Google Scholar

Pul U, Wurm R, Wagner R. The role of LRP and H-NS in transcription regulation: involvement of synergism, allostery and macromolecular crowding. J Mol Biol. 2007 Feb 23;366(3):900–915. https://doi.org/10.1016/j.jmb.2006.11.067 PulU WurmR WagnerR The role of LRP and H-NS in transcription regulation: involvement of synergism, allostery and macromolecular crowding J Mol Biol 2007 Feb 23 366 3 900 915 https://doi.org/10.1016/j.jmb.2006.11.067 10.1016/j.jmb.2006.11.067 Search in Google Scholar

Rajendrakumar CS, Suryanarayana T, Reddy AR. DNA helix destabilization by proline and betaine: possible role in the salinity tolerance process. FEBS Lett. 1997 Jun 30;410(2–3):201–205. https://doi.org/10.1016/s0014-5793(97)00588-7 RajendrakumarCS SuryanarayanaT ReddyAR DNA helix destabilization by proline and betaine: possible role in the salinity tolerance process FEBS Lett 1997 Jun 30 410 2–3 201 205 https://doi.org/10.1016/s0014-5793(97)00588-7 10.1016/S0014-5793(97)00588-7 Search in Google Scholar

Rehan M, Alsohim AS, Abidou H, Rasheed Z, Al Abdulmonem W. Isolation, identification, biocontrol activity, and plant growth promoting capability of a superior Streptomyces tricolor strain HM10. Pol J Microbiol. 2021 Jun;70(2):245–256. https://doi.org/10.33073/pjm-2021-023 RehanM AlsohimAS AbidouH RasheedZ Al AbdulmonemW Isolation, identification, biocontrol activity, and plant growth promoting capability of a superior Streptomyces tricolor strain HM10 Pol J Microbiol 2021 Jun 70 2 245 256 https://doi.org/10.33073/pjm-2021-023 10.33073/pjm-2021-023832698334349814 Search in Google Scholar

Sadeghi A, Soltani BM, Jouzani GS, Karimi E, Nekouei MK, Sadeghizadeh M. Taxonomic study of a salt tolerant Streptomyces sp. strain C-2012 and the effect of salt and ectoine on lon expression level. Microbiol Res. 2014 Feb–Mar;169(2–3):232–238. https://doi.org/10.1016/j.micres.2013.06.010 SadeghiA SoltaniBM JouzaniGS KarimiE NekoueiMK SadeghizadehM Taxonomic study of a salt tolerant Streptomyces sp. strain C-2012 and the effect of salt and ectoine on lon expression level Microbiol Res 2014 Feb–Mar 169 2–3 232 238 https://doi.org/10.1016/j.micres.2013.06.010 10.1016/j.micres.2013.06.01023916596 Search in Google Scholar

Thumar JT, Singh SP. Organic solvent tolerance of an alkaline protease from salt-tolerant alkaliphilic Streptomyces clavuligerus strain Mit-1. J Ind Microbiol Biotechnol. 2009 Feb;36(2):211–218. https://doi.org/10.1007/s10295-008-0487-6 ThumarJT SinghSP Organic solvent tolerance of an alkaline protease from salt-tolerant alkaliphilic Streptomyces clavuligerus strain Mit-1 J Ind Microbiol Biotechnol 2009 Feb 36 2 211 218 https://doi.org/10.1007/s10295-008-0487-6 10.1007/s10295-008-0487-618941814 Search in Google Scholar

Vasavada SH, Thumar, JT, Singh SP. Secretion of a potent antibiotic by salt-tolerant and alkaliphilic actinomycete Streptomyces sannanensis strain RIT-1. Curr Sci. 2006 Nov;91(10):1393–1397. VasavadaSH ThumarJT SinghSP Secretion of a potent antibiotic by salt-tolerant and alkaliphilic actinomycete Streptomyces sannanensis strain RIT-1 Curr Sci 2006 Nov 91 10 1393 1397 Search in Google Scholar

Weber T, Blin K, Duddela S, Krug D, Kim HU, Bruccoleri R, Lee SY, Fischbach MA, Müller R, Wohlleben W, et al. antiSMASH 3.0-a comprehensive resource for the genome mining of biosynthetic gene clusters. Nucleic Acids Res. 2015 Jul 1;43(W1):W237–W243. https://doi.org/10.1093/nar/gkv437 WeberT BlinK DuddelaS KrugD KimHU BruccoleriR LeeSY FischbachMA MüllerR WohllebenW antiSMASH 3.0-a comprehensive resource for the genome mining of biosynthetic gene clusters Nucleic Acids Res 2015 Jul 1 43 W1 W237 W243 https://doi.org/10.1093/nar/gkv437 10.1093/nar/gkv437448928625948579 Search in Google Scholar

Zeng W, Wang D, Kirk W, Hao J. Use of Coniothyrium minitans and other microorganisms for reducing Sclerotinia sclerotiorum. Biol. Control. 2012 Feb;60(2):225–232. https://doi.org/10.1016/j.biocontrol.2011.10.009 ZengW WangD KirkW HaoJ Use of Coniothyrium minitans and other microorganisms for reducing Sclerotinia sclerotiorum Biol. Control 2012 Feb 60 2 225 232 https://doi.org/10.1016/j.biocontrol.2011.10.009 10.1016/j.biocontrol.2011.10.009 Search in Google Scholar

Zhang L, Hashimoto T, Qin B, Hashimoto J, Kozone I, Kawahara T, Okada M, Awakawa T, Ito T, Asakawa Y, et al. Characterization of giant modular PKSs provides insight into genetic mechanism for structural diversification of aminopolyol polyketides. Angew Chem Int Ed Engl. 2017 Feb 6;56(7):1740–1745. https://doi.org/10.1002/anie.201611371 ZhangL HashimotoT QinB HashimotoJ KozoneI KawaharaT OkadaM AwakawaT ItoT AsakawaY Characterization of giant modular PKSs provides insight into genetic mechanism for structural diversification of aminopolyol polyketides Angew Chem Int Ed Engl 2017 Feb 6 56 7 1740 1745 https://doi.org/10.1002/anie.201611371 10.1002/anie.20161137128133950 Search in Google Scholar

Zörb C, Geilfus C M, Dietz K J. Salinity and crop yield. Plant Biol J. 2019 Jan;21(Suppl 1):31–38. https://doi.org/10.1111/plb.12884 ZörbC GeilfusC M DietzK J Salinity and crop yield Plant Biol J 2019 Jan 21 Suppl 1 31 38 https://doi.org/10.1111/plb.12884 10.1111/plb.1288430059606 Search in Google Scholar