Abstract
Streptomyces is the most abundant genus among actinomycetes and holds great potential for sustainable agriculture, both now and in the future, given its role as a source of antibiotics, bioactive compounds, and enzymes. This mini-review discusses the role of these microorganisms in the degradation by enzymatic hydrolysis of lignocellulosic residues during the composting process. Examples of soil amendment with compost bioaugmentated with populations of Streptomyces are reviewed. The advantages derived from the combined use of organic compost and microorganisms of this genus (and other members of Actinobacteria phylum) as biofertilizers to increase plants growth and yield are also presented. Finally, strategies aimed at biocontrol or at the improvement of the capacity for suppression of diseases through an increase in organic matter and Actinobacteria levels are discussed.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
References
Abd-Alla MH, El-Sayed E-SA, Rasmey A-HM (2013) Indole-3-acetic acid (IAA) production by Streptomyces atrovirens isolated from rhizospheric soil in Egypt. J Biol Earth Sci 3:182–193
Afifi MM, Atta HM, Elshanawan AA, Abdoul-rao UM, El-Adly AM (2012) Biosynthesis of hygromycin-B antibiotic by Streptomyces crystallinus AZ151 isolated from Assuit, Egypt. Bacteriol J 2:46–65. https://doi.org/10.3923/bj.2012.46.65
Alam MZ, Manchur MA, Anwar MN (2004) Isolation, purification, characterization of cellulolytic enzymes produced by the isolate Streptomyces omiyaensis. Pak J Biol Sci 7:1647–1653. https://doi.org/10.3923/pjbs.2004.1647.1653
Al-Askar AA, Abdulkhair WM, Rashad YM, Hafez EE, Ghoneem KM, Baka ZA (2014) Streptomyces griseorubens E44G: a potent antagonist isolated from soil in Saudi Arabia. J Pure Appl Microbiol 8:221–230
Aldesuquy HS, Mansour FA, Abo-Hamed SA (1998) Effect of the culture filtrates of Streptomyces on growth and productivity of wheat plants. Folia Microbiol 43:465–470. https://doi.org/10.1007/bf02820792
Alexander M (1991) Introduction to soil microbiology. R.E. Krieger Publishing Company, Malabar, FL
Al-Humiany AU-RAA (2011) Taificidin1 and Taificidin2, two anti-microbial agents isolated from the fermentation broth of Streptomyces roseodistaticus TA15 and Streptomyces lavendofoliae TA17. Res J Microbiol 6:328–342. https://doi.org/10.3923/jm.2011.328.342
Ali A, Guo D, Mahar A, Ma F, Li R, Shen F, Wang P, Zhang Z (2017a) Streptomyces pactum assisted phytoremediation in Zn/Pb smelter contaminated soil of Feng County and its impact on enzymatic activities. Sci Rep 7. https://doi.org/10.1038/srep46087
Ali A, Guo D, Mahar A, Wang P, Ma F, Shen F, Li R, Zhang Z (2017b) Phytoextraction of toxic trace elements by Sorghum bicolor inoculated with Streptomyces pactum (Act12) in contaminated soils. Ecotoxicol Environ Saf 139:202–209. https://doi.org/10.1016/j.ecoenv.2017.01.036
Ali A, Guo D, Mahar A, Wang Z, Muhammad D, Li R, Wang P, Shen F, Xue Q, Zhang Z (2017c) Role of Streptomyces pactum in phytoremediation of trace elements by Brassica juncea in mine polluted soils. Ecotoxicol Environ Saf 144:387–395. https://doi.org/10.1016/j.ecoenv.2017.06.046
Alvarez A, Saez JM, Davila Costa JS, Colin VL, Fuentes MS, Cuozzo SA, Benimeli CS, Polti MA, Amoroso MJ (2017) Actinobacteria: current research and perspectives for bioremediation of pesticides and heavy metals. Chemosphere 166:41–62. https://doi.org/10.1016/j.chemosphere.2016.09.070
Anwar S, Ali B, Sajid I (2016) Screening of rhizospheric actinomycetes for various in-vitro and in-vivo plant growth promoting (PGP) traits and for agroactive compounds. Front Microbiol 7. https://doi.org/10.3389/fmicb.2016.01334
Aparicio JD, Benimeli CS, Almeida CA, Polti MA, Colin VL (2017) Integral use of sugarcane vinasse for biomass production of actinobacteria: potential application in soil remediation. Chemosphere 181:478–484. https://doi.org/10.1016/j.chemosphere.2017.04.107
Aparicio JD, Raimondo EE, Gil RA, Benimeli CS, Polti MA (2018a) Actinobacteria consortium as an efficient biotechnological tool for mixed polluted soil reclamation: experimental factorial design for bioremediation process optimization. J Hazard Mater 342:408–417. https://doi.org/10.1016/j.jhazmat.2017.08.041
Aparicio JD, Saez JM, Raimondo EE, Benimeli CS, Polti MA (2018b) Comparative study of single and mixed cultures of actinobacteria for the bioremediation of co-contaminated matrices. J Environ Chem Eng 6:2310–2318. https://doi.org/10.1016/j.jece.2018.03.030
Araragi M (1979) Comparison of actinomycete flora between tropical and temperate upland farm soils. Soil Sci Plant Nutr 25:245–254. https://doi.org/10.1080/00380768.1979.10433165
Atta HM, El-Sayed AS, El-Desoukey MA, Hassan M, El-Gazar M (2015) Biochemical studies on the Natamycin antibiotic produced by Streptomyces lydicus: fermentation, extraction and biological activities. J Saudi Chem Soc 19:360–371. https://doi.org/10.1016/j.jscs.2012.04.001
August PR, Rahn JA, Flickinger MC, Sherman DH (1996) Inducible synthesis of the mitomycin C resistance gene product (MCRA) from Streptomyces lavendulae. Gene 175:261–267. https://doi.org/10.1016/0378-1119(96)00172-2
Augustine S, Bhavsar S, Kapadnis B (2005) Production of a growth dependent metabolite active against dermatophytes by Streptomyces rochei AK 39. Indian J Med Res 121:164–170
Aung ZH, Takeo Y (2015) Enhanced plant growth and/or nitrogen fixation by leguminous and non-leguminous crops after single or dual inoculation of Streptomyces griseoflavus P4 with Bradyhizobium strains. Afr J Microbiol Res 9:2337–2344. https://doi.org/10.5897/ajmr2015.7796
BacDive (2019a) Streptomyces bellus. https://doi.org/10.13145/bacdive15048.20180622.3
BacDive (2019b) Streptomyces griseiniger. https://doi.org/10.13145/bacdive16422.20180622.3
BacDive (2019c) Streptomyces kanamyceticus. https://doi.org/10.13145/bacdive15333.20180622.3
Balitz DM, O’Herron FA, Bush J, Vyas DM, Nettleton DE, Grulich RE, Bradner WT, Doyle TW, Arnold E, Clardy J (1981) Antitumor agents from Streptomyces anandii: gilvocarcins V, M and E. J Antibiot 34:1544–1555. https://doi.org/10.7164/antibiotics.34.1544
Benlioglu S, Boz O, Yildiz A, Kaskavalci G, Benlioglu K (2005) Alternative soil solarization treatments for the control of soil-borne diseases and weeds of strawberry in the Western Anatolia of Turkey. J Phytopathol 153:423–430. https://doi.org/10.1111/j.1439-0434.2005.00995.x
Bian G-K, Qin S, Yuan B, Zhang Y-J, Xing K, Ju X-Y, Li W-J, Jiang J-H (2012) Streptomyces phytohabitans sp. nov., a novel endophytic actinomycete isolated from medicinal plant Curcuma phaeocaulis. Antonie Van Leeuwenhoek 102:289–296. https://doi.org/10.1007/s10482-012-9737-8
Blumauerová M, Podojil M, Gauze GF, Maksimova TS, Panoš J, Vaněk Z (1980) Spontaneous variability of Streptomyces glomeratus, a producer of the anthracycline antibiotics beromycins. Folia Microbiol 25:207–212. https://doi.org/10.1007/bf02877339
Bogino P, Oliva M, Sorroche F, Giordano W (2013) The role of bacterial biofilms and surface components in plant-bacterial associations. Int J Mol Sci 14:15838–15859. https://doi.org/10.3390/ijms140815838
Box S, Cole M, Yeoman G (1973) Prasinons A and B: potent insecticides from Streptomyces prasinus. J Appl Environ Microbiol 26:699–704
Brar SK, Verma M, Surampalli RY, Misra K, Tyagi RD, Meunier N, Blais JF (2006) Bioremediation of hazardous wastes—a review. Pract Period Hazard Toxic Radioact Waste Manag 10:59–72. https://doi.org/10.1061/(asce)1090-025x(2006)10:2(59)
Briceño G, Vergara K, Schalchli H, Palma G, Tortella G, Fuentes MS, Diez MC (2017) Organophosphorus pesticide mixture removal from environmental matrices by a soil Streptomyces mixed culture. Environ Sci Pollut Res 25:21296–21307. https://doi.org/10.1007/s11356-017-9790-y
Bunet R, Mendes MV, Rouhier N, Pang X, Hotel L, Leblond P, Aigle B (2008) Regulation of the synthesis of the angucyclinone antibiotic alpomycin in Streptomyces ambofaciens by the autoregulator receptor AlpZ and its specific ligand. J Bacteriol 190:3293–3305. https://doi.org/10.1128/jb.01989-07
Burg RW, Miller BM, Baker EE, Birnbaum J, Currie SA, Hartman R, Kong YL, Monaghan RL, Olson G, Putter I, Tunac JB, Wallick H, Stapley EO, Oiwa R, Omura S (1979) Avermectins, new family of potent anthelmintic agents: producing organism and fermentation. Antimicrob Agents Chemother 15:361–367. https://doi.org/10.1128/aac.15.3.361
Burmølle M, Ren D, Bjarnsholt T, Sørensen SJ (2014) Interactions in multispecies biofilms: do they actually matter? Trends Microbiol 22:84–91. https://doi.org/10.1016/j.tim.2013.12.004
Cao S, Wang W, Wang F, Zhang J, Wang Z, Yang S, Xue Q (2016) Drought-tolerant Streptomyces pactum Act12 assist phytoremediation of cadmium-contaminated soil by Amaranthus hypochondriacus: great potential application in arid/semi-arid areas. Environ Sci Pollut Res 23:14898–14907. https://doi.org/10.1007/s11356-016-6636-y
Cao T, Mu S, Lu C, Zhao S, Li D, Yan K, Xiang W, Liu C (2017) Streptomyces amphotericinicus sp. nov., an amphotericin-producing actinomycete isolated from the head of an ant (Camponotus japonicus Mayr). Int J Syst Evol Microbiol 67:4967–4973. https://doi.org/10.1099/ijsem.0.002382
Castillo UF, Jensen JB, Condron MAM, Yaver D, Robison R, Stevens D, Porter H, Hess WM, Teplow DB, Ford EJ, Strobel GA, Albert H (2002) Munumbicins, wide-spectrum antibiotics produced by Streptomyces NRRL 30562 endophytic on Kennedia nigricans. Microbiology 148:2675–2685. https://doi.org/10.1099/00221287-148-9-2675
Cebolla V, Busto J, Ferrer A, Miguel A, Maroto V (2000) Methyl bromide alternatives on horticultural crops. Acta Hortic:237–242. https://doi.org/10.17660/ActaHortic.2000.532.32
Chaiharn M, Pathom-Aree W, Sujada N, Lumyong S (2018) Characterization of phosphate solubilizing Streptomyces as a biofertilizer. Chiang Mai J Sci 45:701–716
Chen W, Huang T, He X, Meng Q, You D, Bai L, Li J, Wu M, Li R, Xie Z, Zhou H, Zhou X, Tan H, Deng Z (2009) Characterization of the polyoxin biosynthetic gene cluster from Streptomyces cacaoi and engineered production of polyoxin H. J Biol Chem 284:10627–10638. https://doi.org/10.1074/jbc.M807534200
Chin-A-Woeng TFC, Bloemberg GV, Mulders IHM, Dekkers LC, Lugtenberg BJJ (2000) Root colonization by phenazine-1-carboxamide-producing bacterium Pseudomonas chlororaphis PCL1391 is essential for biocontrol of tomato foot and root rot. Mol Plant Microbe Interact 13:1340–1345. https://doi.org/10.1094/mpmi.2000.13.12.1340
Chmielewski RAN, Frank JF (2003) Biofilm formation and control in food processing facilities. Compr Rev Food Sci Food Saf 2:22–32. https://doi.org/10.1111/j.1541-4337.2003.tb00012.x
Cuesta G, García-de-la-Fuente R, Abad M, Fornes F (2012) Isolation and identification of actinomycetes from a compost-amended soil with potential as biocontrol agents. J Environ Manag 95:S280–S284. https://doi.org/10.1016/j.jenvman.2010.11.023
Cutler HG, Cutler SJ (1999) Biologically active natural products: agrochemicals. CRC Press, Boca Raton, FL
Da Vinha FNM, Gravina-Oliveira MP, Franco MN, Macrae A, da Silva Bon EP, Nascimento RP, Coelho RRR (2010) Cellulase production by Streptomyces viridobrunneus SCPE-09 using lignocellulosic biomass as inducer substrate. Appl Biochem Biotechnol 164:256–267. https://doi.org/10.1007/s12010-010-9132-8
Daiss N, Lobo MG, Socorro AR, Brückner U, Heller J, Gonzalez M (2007) The effect of three organic pre-harvest treatments on Swiss chard (Beta vulgaris L. var. cycla) quality. Eur Food Res Technol 226:345–353. https://doi.org/10.1007/s00217-006-0543-2
Dam HG, Zhang B, Cai G, Wang H, Li D, Yang X, An X, Zheng X, Tian Y, Zheng W, Zheng T (2014) Streptomyces alboflavus RPS and its novel and high algicidal activity against harmful algal bloom species Phaeocystis globosa. PLoS One 9. https://doi.org/10.1371/journal.pone.0092907
de Jong W, Wösten HAB, Dijkhuizen L, Claessen D (2009) Attachment of Streptomyces coelicolor is mediated by amyloidal fimbriae that are anchored to the cell surface via cellulose. Mol Microbiol 73:1128–1140. https://doi.org/10.1111/j.1365-2958.2009.06838.x
Demain AL (2009) Antibiotics: natural products essential to human health. Med Res Rev 29:821–842. https://doi.org/10.1002/med.20154
Deutsche Forschungsgemeinschaft. Senatskommission zur Beurteilung von Stoffen in der Landwirtschaft (2001) Potentially harmful organisms and substances in feedstuffs and animal faeces. Wiley-VCH; Deutsche Forschungsgemeinschaft, Weinheim, p 5
Diaz LF, De Bertoldi M, Bidlingmaier W (2007) Compost science and technology. Waste management series. Elsevier, Amsterdam, p 8
Dimitrijevic S, Radanovic D, Antic-Mladenovic S, Milutinovic M, Rajilic-Stojanovic M, Dimitrijevic-Brankovic S (2017) Enhanced fertilization effect of a compost obtained from mixed herbs waste inoculated with novel strains of mesophilic bacteria. Hemijska industrija 71:503–513. https://doi.org/10.2298/hemind170327013d
Donlan RM, Costerton JW (2002) Biofilms: survival mechanisms of clinically relevant microorganisms. Clin Microbiol Rev 15:167–193. https://doi.org/10.1128/cmr.15.2.167-193.2002
Doumbou CL, Hamby Salove MK, Crawford DL, Beaulieu C (2001) Actinomycetes, promising tools to control plant diseases and to promote plant growth. Phytoprotection 82. https://doi.org/10.7202/706219ar
Du Y-L, Chen S-F, Cheng L-Y, Shen X-L, Tian Y, Li Y-Q (2009) Identification of a novel Streptomyces chattanoogensis L10 and enhancing its natamycin production by overexpressing positive regulator ScnRII. J Microbiol 47:506–513. https://doi.org/10.1007/s12275-009-0014-0
Dulon S, Parot S, Delia M-L, Bergel A (2006) Electroactive biofilms: new means for electrochemistry. J Appl Electrochem 37:173–179. https://doi.org/10.1007/s10800-006-9250-8
Ekzemplyarov ON (1977) Mycoheptin, an antifungal antibiotic. Pharm Chem J 11:285–289. https://doi.org/10.1007/bf00779104
El-Tarabily KA (2008) Promotion of tomato (Lycopersicon esculentum Mill.) plant growth by rhizosphere competent 1-aminocyclopropane-1-carboxylic acid deaminase-producing streptomycete actinomycetes. Plant Soil 308:161–174. https://doi.org/10.1007/s11104-008-9616-2
El-Tarabily KA, Nassar AH, Sivasithamparam K (2008) Promotion of growth of bean (Phaseolus vulgaris L.) in a calcareous soil by a phosphate-solubilizing, rhizosphere-competent isolate of Micromonospora endolithica. Appl Soil Ecol 39:161–171. https://doi.org/10.1016/j.apsoil.2007.12.005
Espinosa-Urgel M, Kolter R, Ramos J-L (2002) Root colonization by Pseudomonas putida: love at first sight. Microbiology 148:341–343. https://doi.org/10.1099/00221287-148-2-341
Fan M, Xiao X, Guo Y, Zhang J, Wang E, Chen W, Lin Y, Wei G (2018) Enhanced phytoremediation of Robinia pseudoacacia in heavy metal-contaminated soils with rhizobia and the associated bacterial community structure and function. Chemosphere 197:729–740. https://doi.org/10.1016/j.chemosphere.2018.01.102
Feng H, Sun Y, Zhi Y, Mao L, Luo Y, Wei X, Zhou P (2014) Lignocellulose degradation by the isolate of Streptomyces griseorubens JSD-1. Funct Integr Genomics 15:163–173. https://doi.org/10.1007/s10142-014-0425-9
Forján R, Rodríguez-Vila A, Cerqueira B, Covelo EF (2018) Effects of compost and technosol amendments on metal concentrations in a mine soil planted with Brassica juncea L. Environ Sci Pollut Res 25:19713–19727. https://doi.org/10.1007/s11356-018-2173-1
Franco-Correa M, Quintana A, Duque C, Suarez C, Rodríguez MX, Barea J-M (2010) Evaluation of actinomycete strains for key traits related with plant growth promotion and mycorrhiza helping activities. Appl Soil Ecol 45:209–217. https://doi.org/10.1016/j.apsoil.2010.04.007
Fuentes MS, Raimondo EE, Amoroso MJ, Benimeli CS (2017) Removal of a mixture of pesticides by a Streptomyces consortium: influence of different soil systems. Chemosphere 173:359–367. https://doi.org/10.1016/j.chemosphere.2017.01.044
Fuentes MS, Sineli PE, Pons S, de Moreno de LeBlanc A, Benimeli CS, Hill RT, Cuozzo SA (2018) Study of the removal of a pesticides mixture by a Streptomyces strain and their effect on the cytotoxicity of treated systems. J Environ Chem Eng 6:6836–6843. https://doi.org/10.1016/j.jece.2018.10.023
Funayama S, Isono K (2014) Biosynthesis of the polyoxins, nucleoside peptide antibiotics: formation of 5-carboxyuracil nucleosides by Streptomyces cacaoi. Agric Biol Chem 40:1039–1044. https://doi.org/10.1080/00021369.1976.10862152
Getha K, Vikineswary S (2002) Antagonistic effects of Streptomyces violaceusniger strain G10 on Fusarium oxysporum f.sp. cubense race 4: indirect evidence for the role of antibiosis in the antagonistic process. J Ind Microbiol Biotechnol 28:303–310. https://doi.org/10.1038/sj/jim/7000247
Gómez C, Olano C, Palomino-Schätzlein M, Pineda-Lucena A, Carbajo RJ, Braña AF, Méndez C, Salas JA (2012) Novel compounds produced by Streptomyces lydicus NRRL 2433 engineered mutants altered in the biosynthesis of streptolydigin. J Antibiot 65:341–348. https://doi.org/10.1038/ja.2012.37
Goodfellow M, Williams ST, Mordarski M (1988) Actinomycetes in biotechnology. Academic Press, San Diego
Gopalakrishnan S, Pande S, Sharma M, Humayun P, Kiran BK, Sandeep D, Vidya MS, Deepthi K, Rupela O (2011) Evaluation of actinomycete isolates obtained from herbal vermicompost for the biological control of Fusarium wilt of chickpea. Crop Protect 30:1070–1078. https://doi.org/10.1016/j.cropro.2011.03.006
Gopalakrishnan S, Srinivas V, Alekhya G, Prakash B, Kudapa H, Rathore A, Varshney RK (2015) The extent of grain yield and plant growth enhancement by plant growth-promoting broad-spectrum Streptomyces sp. in chickpea. SpringerPlus 4. https://doi.org/10.1186/s40064-015-0811-3
Graf E, Schneider K, Nicholson G, Ströbele M, Jones AL, Goodfellow M, Beil W, RD S¨s, Fiedler H-P (2007) Elloxazinones A and B, new aminophenoxazinones from Streptomyces griseus Acta 2871. J Antibiot 60:277–284. https://doi.org/10.1038/ja.2007.35
Grigorevski de Lima AL, Pires do Nascimento R, da Silva Bon EP, Coelho RRR (2005) Streptomyces drozdowiczii cellulase production using agro-industrial by-products and its potential use in the detergent and textile industries. Enzym Microb Technol 37:272–277. https://doi.org/10.1016/j.enzmictec.2005.03.016
Harir M, Bendif H, Bellahcene M, Fortas RPZ (2018) Streptomyces secondary metabolites. In: Enany S (ed) Basic biology and applications of actinobacteria. InTechOpen, pp 99–121. https://doi.org/10.5772/intechopen.79890
Harrison PH, Noguchi H, Vederas JC (1986) Biosynthesis of polyene antibiotics: intact incorporation of carbon-13 labeled octanoate into fungichromin by Streptomyces cellulosae. J Am Chem Soc 108:3833–3834. https://doi.org/10.1021/ja00273a050
Hibbing ME, Fuqua C, Parsek MR, Peterson SB (2009) Bacterial competition: surviving and thriving in the microbial jungle. Nat Rev Microbiol 8:15–25. https://doi.org/10.1038/nrmicro2259
Hillis DM, Book AJ, Lewin GR, McDonald BR, Takasuka TE, Wendt-Pienkowski E, Doering DT, Suh S, Raffa KF, Fox BG, Currie CR (2016) Evolution of high cellulolytic activity in symbiotic Streptomyces through selection of expanded gene content and coordinated gene expression. PLoS Biol 14. https://doi.org/10.1371/journal.pbio.1002475
Hochstein FA, Murai K (1954) Magnamycin B, a second antibiotic from Streptomyces halstedii. J Am Chem Soc 76:5080–5083. https://doi.org/10.1021/ja01649a020
Hotta K, Ogata T, Ishikawa JUN, Okanishi M, Mizuno S, MoRiOka M, Naganawa H, Okami Y (1996) Mechanismm of multiple aminoglycoside resistance of kasugamycin-producing Streptomyces kasugaensis MB273: involvement of two types of acetyltransferases in resistance to astromicin group antibiotics. J Antibiot 49:682–688. https://doi.org/10.7164/antibiotics.49.682
Htwe AZ, Yamakawa T (2016) Low-density co-inoculation with Bradyrhizobium japonicum SAY3-7 and Streptomyces griseoflavus P4 promotes plant growth and nitrogen fixation in soybean cultivars. Am J Plant Sci 7:1652–1661. https://doi.org/10.4236/ajps.2016.712156
Htwe AZ, Moh SM, Moe K, Yamakawa T (2018) Effects of co-inoculation of Bradyrhizobium japonicum SAY3-7 and Streptomyces griseoflavus P4 on plant growth, nodulation, nitrogen fixation, nutrient uptake, and yield of soybean in a field condition. Soil Sci Plant Nutr 64:222–229. https://doi.org/10.1080/00380768.2017.1421436
Huang X, Zhang N, Yong X, Yang X, Shen Q (2012) Biocontrol of Rhizoctonia solani damping-off disease in cucumber with Bacillus pumilus SQR-N43. Microbiol Res 167:135–143. https://doi.org/10.1016/j.micres.2011.06.002
Hwang BK, Lim SW, Kim BS, Lee JY, Moon SS (2001) Isolation and in vivo and in vitro antifungal activity of phenylacetic acid and sodium phenylacetate from Streptomyces humidus. Appl Environ Microbiol 67:3739–3745. https://doi.org/10.1128/aem.67.8.3739-3745.2001
Igarashi Y, Iida T, Sasaki T, Saito N, Yoshida R, Furumai T (2002) Isolation of actinomycetes from live plants and evaluation of antiphytopathogenic activity of their metabolites. Actinomycetologica 16:9–13. https://doi.org/10.3209/saj.16_9
Il’ina AV, Tatarinova N, Tikhonov VE, Varlamov VP (2000) Extracellular proteinases and chitinases, produced by a Streptomyces kurssanovii culture. Prikl Biokhim Mikrobiol 36:173–177
Irdani T, Perito B, Mastromei G (1996) Characterization of a Streptomyces rochei endoglucanasea. Ann N Y Acad Sci 782:173–181. https://doi.org/10.1111/j.1749-6632.1996.tb40558.x
Jang H-D, Chang K-S (2005) Thermostable cellulases from Streptomyces sp.: scale-up production in a 50-l fermenter. Biotechnol Lett 27:239–242. https://doi.org/10.1007/s10529-004-8356-5
Janssen GR, Ward JM, Bibb MJ (1989) Unusual transcriptional and translational features of the aminoglycoside phosphotransferase gene (aph) from Streptomyces fradiae. Genes Dev 3:415–429. https://doi.org/10.1101/gad.3.3.415
Jezequel K, Lebeau T (2008) Soil bioaugmentation by free and immobilized bacteria to reduce potentially phytoavailable cadmium. Bioresour Technol 99:690–698. https://doi.org/10.1016/j.biortech.2007.02.002
Ji Z, Qiao G, Wei S, Fan L, Wu W (2012) Isolation and characterization of two novel antibacterial cyclic hexapeptides from Streptomyces alboflavus 313. Chem Biodivers 9:1567–1578. https://doi.org/10.1002/cbdv.201100364
Jiang H, Wang Y-Y, Ran X-X, Fan W-M, Jiang X-H, Guan W-J, Li Y-Q (2013) Improvement of natamycin production by engineering of phosphopantetheinyl transferases in Streptomyces chattanoogensis L10. Appl Environ Microbiol 79:3346–3354. https://doi.org/10.1128/aem.00099-13
Kakinuma K, Hanson CA, Rinehart KL (1976) Spectinabilin, a new nitro-containing metabolite isolated from Streptomyces spectabilis. Tetrahedron 32:217–222. https://doi.org/10.1016/0040-4020(76)87004-4
Kanini GS, Katsifas EA, Savvides AL, Karagouni AD (2013) Streptomyces rochei ACTA1551, an indigenous Greek isolate studied as a potential biocontrol agent against Fusarium oxysporum f. sp. lycopersici. Biomed Res Int 2013:1–10. https://doi.org/10.1155/2013/387230
Kato S, Shindo K, Kawai H, Odagawa A, Matsuoka M, Mochizuki J (1993) Pyrrolostatin, a novel lipid peroxidation inhibitor from Streptomyces chrestomyceticus. Taxonomy, fermentation, isolation, structure elucidation and biological properties. J Antibiot 46:892–899. https://doi.org/10.7164/antibiotics.46.892
Kawasaki T, Sakurai F, S-y N, Hayakawa Y (2009) Prodigiosin biosynthesis gene cluster in the roseophilin producer Streptomyces griseoviridis. J Antibiot 62:271–276. https://doi.org/10.1038/ja.2009.27
Khamna S, Yokota A, Lumyong S (2008) Actinomycetes isolated from medicinal plant rhizosphere soils: diversity and screening of antifungal compounds, indole-3-acetic acid and siderophore production. World J Microbiol Biotechnol 25:649–655. https://doi.org/10.1007/s11274-008-9933-x
Khamna S, Yokota A, Peberdy JF, Lumyong S (2010) Indole-3-acetic acid production by Streptomyces sp. isolated from some Thai medicinal plant rhizosphere soils. EurAsian J Biosci:23–32. https://doi.org/10.5053/ejobios.2010.4.0.4
Khiyami MA, Pometto AL, Brown RC (2005) Detoxification of corn Stover and corn starch pyrolysis liquors by Pseudomonas putida and Streptomyces setonii suspended cells and plastic compost support biofilms. J Agric Food Chem 53:2978–2987. https://doi.org/10.1021/jf048224e
Kim YM, Kim JH (2004) Formation and dispersion of mycelial pellets of Streptomyces coelicolor A3(2). J Microbiol 42:64–67
Kim Y, Kim H, Beuchat LR, Ryu J-H (2019) Inhibition of Listeria monocytogenes using biofilms of non-pathogenic soil bacteria (Streptomyces spp.) on stainless steel under desiccated condition. Food Microbiol 79:61–65. https://doi.org/10.1016/j.fm.2018.11.007
Klausen M, Heydorn A, Ragas P, Lambertsen L, Aaes-Jørgensen A, Molin S, Tolker-Nielsen T (2003) Biofilm formation by Pseudomonas aeruginosa wild type, flagella and type IV pili mutants. Mol Microbiol 48:1511–1524. https://doi.org/10.1046/j.1365-2958.2003.03525.x
Klein E, Ofek M, Katan J, Minz D, Gamliel A (2013) Soil suppressiveness to Fusarium disease: shifts in root microbiome associated with reduction of pathogen root colonization. Phytopathology 103:23–33. https://doi.org/10.1094/phyto-12-11-0349
Kpomblekou-A K, Tabatabai MA (1994) Effect of organic acids on release of phosphorus from phosphate rocks. Soil Sci 158:442–453. https://doi.org/10.1097/00010694-199415860-00006
Kraemer SM, Crowley DE, Kretzschmar R (2006) Geochemical aspects of phytosiderophore-promoted iron acquisition by plants. Adv Agron 91:1–46. https://doi.org/10.1016/s0065-2113(06)91001-3
Lang Z, Qi D, Dong J, Ren L, Zhu Q, Huang W, Liu Y, Lu D (2018) Isolation and characterization of a quinclorac-degrading Actinobacteria Streptomyces sp. strain AH-B and its implication on microecology in contaminated soil. Chemosphere 199:210–217. https://doi.org/10.1016/j.chemosphere.2018.01.133
Laskin AI, Lechevalier HA (1977) CRC handbook of microbiology, 2nd edn. CRC Press, Boca Raton, FL
Lee JY (2005) Streptomyces koyangensis sp. nov., a novel actinomycete that produces 4-phenyl-3-butenoic acid. Int J Syst Evol Microbiol 55:257–262. https://doi.org/10.1099/ijs.0.63168-0
Lee JY, Lee JY, Moon SS, Hwang BK (2005) Isolation and antifungal activity of 4-phenyl-3-butenoic acid from Streptomyces koyangensis strain VK-A60. J Agric Food Chem 53:7696–7700. https://doi.org/10.1021/jf050957r
Li ZHE, Rawlings BJ, Harrison PH, Vederas JC (1989) Production of new polyene antibiotics by Streptomyces cellulosae after addition of ethyl(Z)-16-phenylhexadec-9-enoate. J Antibiot 42:577–584. https://doi.org/10.7164/antibiotics.42.577
Lian Q, Zhang J, Gan L, Ma Q, Zong Z, Wang Y (2017) The biocontrol efficacy of Streptomyces pratensis LMM15 on Botrytis cinerea in tomato. Biomed Res Int 2017:1–11. https://doi.org/10.1155/2017/9486794
Lim S-W, Kim J-D, Kim B-S, Hwang B-K (2000) Isolation and numerical identification of Streptomyces humidus strain S5-55 antagonistic to plant pathogenic fungi. Plant Pathol J 16:189–199
Liu C, Wang X, Yan Y, Wang J, Zhang B, Zhang J, Xiang W (2012) Streptomyces heilongjiangensis sp. nov., a novel actinomycete that produces borrelidin isolated from the root surface of soybean [Glycine max (L.) Merr]. Int J Syst Evol Microbiol 63:1030–1036. https://doi.org/10.1099/ijs.0.041483-0
Liu Y, Ryu H, Ge B, Pan G, Sun L, Park K, Zhang K (2014) Improvement of Wuyiencin biosynthesis in Streptomyces wuyiensis CK-15 by identification of a key regulator, WysR. J Microbiol Biotechnol 24:1644–1653. https://doi.org/10.4014/jmb.1405.05017
Locatelli FM, Goo K-S, Ulanova D (2016) Effects of trace metal ions on secondary metabolism and the morphological development of streptomycetes. Metallomics 8:469–480. https://doi.org/10.1039/c5mt00324e
Luo L, Cai J, Wang C, Lin J, Du X, Zhou A, Xiang M (2016) Purification and characterization of an alkaliphilic endo-xylanase from Streptomyces althioticus LMZM and utilization in the pulp paper industry. J Chem Technol Biotechnol 91:1093–1098. https://doi.org/10.1002/jctb.4690
Ma S-C, Zhang H-B, Ma S-T, Wang R, Wang G-X, Shao Y, Li C-X (2015) Effects of mine wastewater irrigation on activities of soil enzymes and physiological properties, heavy metal uptake and grain yield in winter wheat. Ecotoxicol Environ Saf 113:483–490. https://doi.org/10.1016/j.ecoenv.2014.12.031
Macagnan D, Romeiro RS, Pomella AWV, deSouza JT (2008) Production of lytic enzymes and siderophores, and inhibition of germination of basidiospores of Moniliophthora (ex Crinipellis) perniciosa by phylloplane actinomycetes. Biol Control 47:309–314. https://doi.org/10.1016/j.biocontrol.2008.08.016
Magae J, Kataoka T, Yamashita M, Tsuji RF, Lee M-H, Yamasaki M, Nagai K (1993) Suppression of killer T cell induction by prodigiosin 25-C. In: Animal cell technology: basic & applied aspects. pp 149–154. doi:https://doi.org/10.1007/978-94-011-2044-9_21
Mahan KM, Klingeman DM, Hettich RL, Parry RJ, Graham DE (2016) Draft genome sequence of Streptomyces vitaminophilus ATCC 31673, a producer of pyrrolomycin antibiotics, some of which contain a nitro group. Genome Announc 4. https://doi.org/10.1128/genomeA.01582-15
Maheswari MU, Chandra TS (2000) Production and potential applications of a xylanase from a new strain of Streptomyces cuspidosporus. World J Microbiol Biotechnol 16:257–263. https://doi.org/10.1023/a:1008945931108
Mansfield J, Genin S, Magori S, Citovsky V, Sriariyanum M, Ronald P, Dow MAX, Verdier V, Beer SV, Machado MA, Toth IAN, Salmond G, Foster GD (2012) Top 10 plant pathogenic bacteria in molecular plant pathology. Mol Plant Pathol 13:614–629. https://doi.org/10.1111/j.1364-3703.2012.00804.x
Marques APGC, Pires C, Moreira H, Rangel AOSS, Castro PML (2010) Assessment of the plant growth promotion abilities of six bacterial isolates using Zea mays as indicator plant. Soil Biol Biochem 42:1229–1235. https://doi.org/10.1016/j.soilbio.2010.04.014
McGhee GC, Sundin GW (2011) Evaluation of kasugamycin for fire blight management, effect on nontarget bacteria, and assessment of kasugamycin resistance potential in Erwinia amylovora. Phytopathology 101:192–204. https://doi.org/10.1094/phyto-04-10-0128
Mehta CM, Palni U, Franke-Whittle IH, Sharma AK (2014) Compost: its role, mechanism and impact on reducing soil-borne plant diseases. Waste Manag 34:607–622. https://doi.org/10.1016/j.wasman.2013.11.012
Miao V (2005) Daptomycin biosynthesis in Streptomyces roseosporus: cloning and analysis of the gene cluster and revision of peptide stereochemistry. Microbiology 151:1507–1523. https://doi.org/10.1099/mic.0.27757-0
Miyadoh S, Shomura T, Ito T, Niida T (1983) Streptomyces sulfonofaciens sp. nov. Int J Syst Bacteriol 33:321–324. https://doi.org/10.1099/00207713-33-2-321
Mohandas S, Poovarasan S, Panneerselvam P, Saritha B, Upreti KK, Kamal R, Sita T (2013) Guava (Psidium guajava L.) rhizosphere Glomus mosseae spores harbor actinomycetes with growth promoting and antifungal attributes. Sci Hortic 150:371–376. https://doi.org/10.1016/j.scienta.2012.11.019
Monier JM, Lindow SE (2003) Differential survival of solitary and aggregated bacterial cells promotes aggregate formation on leaf surfaces. Proc Natl Acad Sci 100:15977–15982. https://doi.org/10.1073/pnas.2436560100
Morales DK, Ocampo W, Zambrano MM (2007) Efficient removal of hexavalent chromium by a tolerant Streptomyces sp. affected by the toxic effect of metal exposure. J Appl Microbiol 103:2704–2712. https://doi.org/10.1111/j.1365-2672.2007.03510.x
Murakami T, Anzai H, Imai S, Satoh A, Nagaoka K, Thompson CJ (1986) The bialaphos biosynthetic genes of Streptomyces hygroscopicus: molecular cloning and characterization of the gene cluster. MGG Mol Gen Genet 205:42–53. https://doi.org/10.1007/bf02428031
Murakami S, Harada S, Takahashi Y, Naganawa H, Takeuchi T, Aoyagi T (2008) Piperastatin B: A new selective serine carboxypeptidase inhibitor from Streptomyces lavendofoliae MJ908-WF13. J Enzym Inhib 11:51–66. https://doi.org/10.3109/14756369609038222
Nascimento RP, Junior NA, Pereira Jr N, Bon EPS, Coelho RRR (2009) Brewer’s spent grain and corn steep liquor as substrates for cellulolytic enzymes production by Streptomyces malaysiensis. Lett Appl Microbiol 48:529–535. https://doi.org/10.1111/j.1472-765X.2009.02575.x
Neilan B, Hao C, Huang S, Deng Z, Zhao C, Yu Y (2014) Mining of the pyrrolamide antibiotics analogs in Streptomyces netropsis reveals the amidohydrolase-dependent “iterative strategy” underlying the pyrrole polymerization. PLoS One 9. https://doi.org/10.1371/journal.pone.0099077
Nguyen TM, Kim J (2015) Description of Streptomyces fabae sp. nov., a producer of antibiotics against microbial pathogens, isolated from soybean (Glycine max) rhizosphere soil. Int J Syst Evol Microbiol 65:4151–4156. https://doi.org/10.1099/ijsem.0.000551
Ohnishi Y, Ishikawa J, Hara H, Suzuki H, Ikenoya M, Ikeda H, Yamashita A, Hattori M, Horinouchi S (2008) Genome sequence of the streptomycin-producing microorganism Streptomyces griseus IFO 13350. J Bacteriol 190:4050–4060. https://doi.org/10.1128/jb.00204-08
Ostash B, Gren T, Hrubskyy Y, Tistechok S, Beshley S, Baranov V, Fedorenko V (2014) Cultivable actinomycetes from rhizosphere of birch (Betula pendula) growing on a coal mine dump in Silets, Ukraine. J Basic Microbiol 54:851–857. https://doi.org/10.1002/jobm.201200551
Park JO, El-Tarabily KA, Ghisalberti EL, Sivasithamparam K (2002) Pathogenesis of Streptoverticillium albireticuli on Caenorhabditis elegans and its antagonism to soil-borne fungal pathogens. Lett Appl Microbiol 35:361–365. https://doi.org/10.1046/j.1472-765x.2002.01194.x
Parot S, Délia M-L, Bergel A (2008) Forming electrochemically active biofilms from garden compost under chronoamperometry. Bioresour Technol 99:4809–4816. https://doi.org/10.1016/j.biortech.2007.09.047
Passari AK, Mishra VK, Saikia R, Gupta VK, Singh BP (2015) Isolation, abundance and phylogenetic affiliation of endophytic actinomycetes associated with medicinal plants and screening for their in vitro antimicrobial biosynthetic potential. Front Microbiol 6. https://doi.org/10.3389/fmicb.2015.00273
Passari AK, Chandra P, Zothanpuia MVK, Leo VV, Gupta VK, Kumar B, Singh BP (2016) Detection of biosynthetic gene and phytohormone production by endophytic actinobacteria associated with Solanum lycopersicum and their plant-growth-promoting effect. Res Microbiol 167:692–705. https://doi.org/10.1016/j.resmic.2016.07.001
Payero TD, Vicente CM, Rumbero Á, Barreales EG, Santos-Aberturas J, de Pedro A, Aparicio JF (2015) Functional analysis of filipin tailoring genes from Streptomyces filipinensis reveals alternative routes in filipin III biosynthesis and yields bioactive derivatives. Microb Cell Factories 14. https://doi.org/10.1186/s12934-015-0307-4
Peng D, Li S, Wang J, Chen C, Zhou M (2014) Integrated biological and chemical control of rice sheath blight by Bacillus subtilis NJ-18 and jinggangmycin. Pest Manag Sci 70:258–263. https://doi.org/10.1002/ps.3551
Pernodet JL, Alegre MT, Blondelet-Rouault MH, Guerineau M (1993) Resistance to spiramycin in Streptomyces ambofaciens, the producer organism, involves at least two different mechanisms. J Gen Microbiol 139:1003–1011. https://doi.org/10.1099/00221287-139-5-1003
Peterson RM, Huang T, Rudolf Jeffrey D, Smanski Michael J, Shen B (2014) Mechanisms of self-resistance in the platensimycin- and platencin-producing Streptomyces platensis MA7327 and MA7339 strains. Chem Biol 21:389–397. https://doi.org/10.1016/j.chembiol.2014.01.005
Phieler R, Merten D, Roth M, Büchel G, Kothe E (2015) Phytoremediation using microbially mediated metal accumulation in Sorghum bicolor. Environ Sci Pollut Res 22:19408–19416. https://doi.org/10.1007/s11356-015-4471-1
Prakash D, Sharma G (2014) Phytochemicals of nutraceutical importance. CABI/CAB International, Wallingford
Pugliese M, Liu B, Gullino ML, Garibaldi A (2008) Selection of antagonists from compost to control soil-borne pathogens. J Plant Dis Prot 115:220–228. https://doi.org/10.1007/BF03356267
Ramírez P, Coha JM (2003) Enzymatic degradation of cellulose for thermophilic actinomycete: isolation, characterization and cellulolytic activity determination. Rev Peru Biol 10:67–77
Rashad FM, Saleh WD, Moselhy MA (2010) Bioconversion of rice straw and certain agro-industrial wastes to amendments for organic farming systems: 1. Composting, quality, stability and maturity indices. Bioresour Technol 101:5952–5960. https://doi.org/10.1016/j.biortech.2010.02.103
Rashad FM, Fathy HM, El-Zayat AS, Elghonaimy AM (2015) Isolation and characterization of multifunctional Streptomyces species with antimicrobial, nematicidal and phytohormone activities from marine environments in Egypt. Microbiol Res 175:34–47. https://doi.org/10.1016/j.micres.2015.03.002
Reisner A, Haagensen JAJ, Schembri MA, Zechner EL, Molin S (2003) Development and maturation of Escherichia coli K-12 biofilms. Mol Microbiol 48:933–946. https://doi.org/10.1046/j.1365-2958.2003.03490.x
Rey T, Dumas B (2017) Plenty is no plague: Streptomyces symbiosis with crops. Trends Plant Sci 22:30–37. https://doi.org/10.1016/j.tplants.2016.10.008
Saez JM, Casillas García V, Benimeli CS (2017) Improvement of lindane removal by Streptomyces sp. M7 by using stable microemulsions. Ecotoxicol Environ Saf 144:351–359. https://doi.org/10.1016/j.ecoenv.2017.06.026
Sanglier JJ, Haag H, Huck TA, Fehr T (1993) Novel bioactive compounds from Actinomycetes: a short review (1988–1992). Res Microbiol 144:633–642. https://doi.org/10.1016/0923-2508(93)90066-b
Santos JFD, Sousa CDS, Soares ACF, Lima FDS, Barbosa DHSG (2016) Actinobacteria and organic fertilizers for management of the nematode Scutellonema bradys in yam plants. Rev Caatinga 29:548–558. https://doi.org/10.1590/1983-21252016v29n304rc
Sathya A, Vijayabharathi R, Srinivas V, Gopalakrishnan S (2016) Plant growth-promoting actinobacteria on chickpea seed mineral density: an upcoming complementary tool for sustainable biofortification strategy. 3 Biotech 6. https://doi.org/10.1007/s13205-016-0458-y
Sathya A, Vijayabharathi R, Gopalakrishnan S (2017) Plant growth-promoting actinobacteria: a new strategy for enhancing sustainable production and protection of grain legumes. 3 Biotech 7. https://doi.org/10.1007/s13205-017-0736-3
Satpathy S, Sen SK, Pattanaik S, Raut S (2016) Review on bacterial biofilm: an universal cause of contamination. Biocatal Agric Biotechnol 7:56–66. https://doi.org/10.1016/j.bcab.2016.05.002
Sauer K, Camper AK, Ehrlich GD, Costerton JW, Davies DG (2002) Pseudomonas aeruginosa displays multiple phenotypes during development as a biofilm. J Bacteriol 184:1140–1154. https://doi.org/10.1128/jb.184.4.1140-1154.2002
Schatz A, Bugle E, Waksman SA (1944) Streptomycin, a substance exhibiting antibiotic activity against Gram-positive and Gram-negative bacteria. Exp Biol Med 55:66–69. https://doi.org/10.3181/00379727-55-14461
Schirawski J, Perlin M (2018) Plant–microbe interaction 2017—the good, the bad and the diverse. Int J Mol Sci 19. https://doi.org/10.3390/ijms19051374
Schrey SD, Tarkka MT (2008) Friends and foes: streptomycetes as modulators of plant disease and symbiosis. Antonie Van Leeuwenhoek 94:11–19. https://doi.org/10.1007/s10482-008-9241-3
Schütze E, Klose M, Merten D, Nietzsche S, Senftleben D, Roth M, Kothe E (2014) Growth of streptomycetes in soil and their impact on bioremediation. J Hazard Mater 267:128–135. https://doi.org/10.1016/j.jhazmat.2013.12.055
Semedo LTAS (2004) Streptomyces drozdowiczii sp. nov., a novel cellulolytic streptomycete from soil in Brazil. Int J Syst Evol Microbiol 54:1323–1328. https://doi.org/10.1099/ijs.0.02844-0
Sharma A, Saha TN, Arora A, Shah R, Nain L (2017) Efficient microorganism compost benefits plant growth and improves soil health in calendula and marigold. Horticult Plant J 3:67–72. https://doi.org/10.1016/j.hpj.2017.07.003
Sheldon PJ, Mao Y, He M, Sherman DH (1999) Mitomycin resistance in Streptomyces lavendulae includes a novel drug-binding-protein-dependent export system. J Bacteriol 181:2507–2512
Shen T, Wang C, Yang H, Deng Z, Wang S, Shen B, Shen Q (2016) Identification, solid-state fermentation and biocontrol effects of Streptomyces hygroscopicus B04 on strawberry root rot. Appl Soil Ecol 103:36–43. https://doi.org/10.1016/j.apsoil.2016.02.016
Shi X, Zhu X (2009) Biofilm formation and food safety in food industries. Trends Food Sci Technol 20:407–413. https://doi.org/10.1016/j.tifs.2009.01.054
Shi L, Nwet TT, Ge B, Zhao W, Liu B, Cui H, Zhang K (2018) Antifungal and plant growth-promoting activities of Streptomyces roseoflavus strain NKZ-259. Biol Control 125:57–64. https://doi.org/10.1016/j.biocontrol.2018.06.012
Simões M, Simões LC, Vieira MJ (2010) A review of current and emergent biofilm control strategies. LWT Food Sci Technol 43:573–583. https://doi.org/10.1016/j.lwt.2009.12.008
Singh SP, Gaur R (2016) Evaluation of antagonistic and plant growth promoting activities of chitinolytic endophytic actinomycetes associated with medicinal plants against Sclerotium rolfsii in chickpea. J Appl Microbiol 121:506–518. https://doi.org/10.1111/jam.13176
Singh O, Srivastava S (1998) Dictionary of entomology, plant pathology and nematology. Concept Publishing Company, New Delhi
Singh A, Gupta R, Srivastava M, Gupta MM, Pandey R (2016) Microbial secondary metabolites ameliorate growth, in planta contents and lignification in Withania somnifera (L.) Dunal. Physiol Mol Biol Plants 22:253–260. https://doi.org/10.1007/s12298-016-0359-x
Singh RP, Manchanda G, Maurya IK, Maheshwari NK, Tiwari PK, Rai AR (2019) Streptomyces from rotten wheat straw endowed the high plant growth potential traits and agro-active compounds. Biocatal Agric Biotechnol 17:507–513. https://doi.org/10.1016/j.bcab.2019.01.014
Smanski MJ, Peterson RM, Rajski SR, Shen B (2009) Engineered Streptomyces platensis strains that overproduce antibiotics platensimycin and platencin. Antimicrob Agents Chemother 53:1299–1304. https://doi.org/10.1128/aac.01358-08
Strom PF (1985) Identification of thermophilic bacteria in solid-waste composting. Appl Environ Microbiol 50:906–913
Sveshnikova M, Timuk O, Borisova V, Fedorova G (1983) New species of actinomycete Streptomyces variegatus sp. nov. synthesizing an antibiotic of the alpha-hydroxyketopentaene group. Antibiotiki 28:723–728
Takahashi Y (2002) Streptomyces avermectinius sp. nov., an avermectin-producing strain. Int J Syst Evol Microbiol 52:2163–2168. https://doi.org/10.1099/ijs.0.02237-0
Tamreihao K, Ningthoujam DS, Nimaichand S, Singh ES, Reena P, Singh SH, Nongthomba U (2016) Biocontrol and plant growth promoting activities of a Streptomyces corchorusii strain UCR3-16 and preparation of powder formulation for application as biofertilizer agents for rice plant. Microbiol Res 192:260–270. https://doi.org/10.1016/j.micres.2016.08.005
Tikhonov VE, Radigina LA, Yamskov IA, Gulyaeva ND, Ilyina AV, Anisimova MV, Varlamov VP, Tatarinova NY (1998) Affinity purification of major chitinases produced by Streptomyces kurssanovii. Enzym Microb Technol 22:82–85. https://doi.org/10.1016/s0141-0229(97)00099-9
Timková I, Sedláková-Kaduková J, Pristaš P (2018) Biosorption and bioaccumulation abilities of actinomycetes/streptomycetes isolated from metal contaminated sites. Separations 5. https://doi.org/10.3390/separations5040054
Trejo WH, Dean LD, Pluscec J, Meyers E, Brown WE (1977) Streptomyces laurentii, a new species producing thiostrepton. J Antibiot 30:639–643. https://doi.org/10.7164/antibiotics.30.639
Trejo-Estrada SR, Paszczynski A, Crawford DL (1998) Antibiotics and enzymes produced by the biocontrol agent Streptomyces violaceusniger YCED-9. J Ind Microbiol Biotechnol 21:81–90. https://doi.org/10.1038/sj.jim.2900549
Ueberschaar N, Ndejouong BLST, Ding L, Maier A, Fiebig H-H, Hertweck C (2011) Hydrazidomycins, cytotoxic alkylhydrazides from Streptomyces atratus. Bioorg Med Chem Lett 21:5839–5841. https://doi.org/10.1016/j.bmcl.2011.07.108
Uri J, Békési I (1958) Flavofungin, a new crystalline antifungal antibiotic: origin and biological properties. Nature 181:908–908. https://doi.org/10.1038/181908a0
Uyeda M, Mizukami M, Yokomizo K, Suzuki K (2014) Pentalenolactone I and hygromycin A, immunosuppressants produced by Streptomyces filipinensis and Streptomyces hygroscopicus. Biosci Biotechnol Biochem 65:1252–1254. https://doi.org/10.1271/bbb.65.1252
van Balken JAM (1997) Biotechnological innovations in chemical synthesis. Biotechnology by open learning. Butterworth Heinemann, Oxford
Ventorino V, Ionata E, Birolo L, Montella S, Marcolongo L, de Chiaro A, Espresso F, Faraco V, Pepe O (2016) Lignocellulose-adapted endo-cellulase producing Streptomyces strains for bioconversion of cellulose-based materials. Front Microbiol 7. https://doi.org/10.3389/fmicb.2016.02061
Verma S, Sharma A, Kumar R, Kaur C, Arora A, Shah R, Nain L (2015) Improvement of antioxidant and defense properties of tomato (var. Pusa Rohini) by application of bioaugmented compost. Saudi J Biol Sci 22:256–264. https://doi.org/10.1016/j.sjbs.2014.11.003
Vining LC (2014) Chapter 5 - Peptides. In: Tsao GT (ed) Annual reports on fermentation processes, vol 4, 2nd edn. Elsevier, New York, pp 123–163. https://doi.org/10.1016/B978-0-12-040304-2.50012-6
Virolle M-J, Passari AK, Mishra VK, Gupta VK, Yadav MK, Saikia R, Singh BP (2015) In vitro and in vivo plant growth promoting activities and DNA fingerprinting of antagonistic endophytic actinomycetes associates with medicinal plants. PLoS One 10. https://doi.org/10.1371/journal.pone.0139468
Vurukonda SSKP, Giovanardi D, Stefani E (2018) Plant growth promoting and biocontrol activity of Streptomyces spp. as endophytes. Int J Mol Sci 19. https://doi.org/10.3390/ijms19040952
Waksman SA, Lechevalier HA (1949) Neomycin, a new antibiotic active against streptomycin-resistant bacteria, including tuberculosis organisms. Science 109:305–307. https://doi.org/10.1126/science.109.2830.305
Wan Z, Fang W, Shi L, Wang K, Zhang Y, Zhang Z, Wu Z, Yang Z, Gu Y (2014) Novonestmycins A and B, two new 32-membered bioactive macrolides from Streptomyces phytohabitans HBERC-20821. J Antibiot 68:185–190. https://doi.org/10.1038/ja.2014.123
Wang C (2018) Phosphorus-release dynamics by phosphate solubilizing actinomycetes and its enhancement of growth and yields in maize. Int J Agric Biol 437–444. doi:https://doi.org/10.17957/ijab/15.0554
Wang C, Wang Z, Qiao X, Li Z, Li F, Chen M, Wang Y, Huang Y, Cui H (2013a) Antifungal activity of volatile organic compounds from Streptomyces alboflavus TD-1. FEMS Microbiol Lett 341:45–51. https://doi.org/10.1111/1574-6968.12088
Wang X-J, Zhang J, Wang J-D, Qian P-T, Liu C-X, Xiang W-S (2013b) Novel cyclopentenone derivatives produced by a rare actinobacterial strain Actinoalloteichus nanshanensis sp. nov. NEAU 119. Nat Prod Res 27:1863–1869. https://doi.org/10.1080/14786419.2013.771349
Wang H, Han L, Feng J, Zhang X (2015) Evaluation of two Streptomyces spp. and compost for growth promotion and biocontrol potential against Rhizoctonia solani on pepper. Biocontrol Sci Technol 25:852–857. https://doi.org/10.1080/09583157.2015.1015485
Wang S, Liang Y, Shen T, Yang H, Shen B (2016) Biological characteristics of Streptomyces albospinus CT205 and its biocontrol potential against cucumber Fusarium wilt. Biocontrol Sci Technol 26:951–963. https://doi.org/10.1080/09583157.2016.1172203
Watve M, Tickoo R, Jog M, Bhole B (2001) How many antibiotics are produced by the genus Streptomyces? Arch Microbiol 176:386–390. https://doi.org/10.1007/s002030100345
Wegler R (1981) Insektizide · Bakterizide · Oomyceten-Fungizide / Biochemische und biologische Methoden · Naturstoffe / Insecticides · Bactericides · OOMYCETE Fungicides / Biochemical and Biological Methods · Natural Products, vol 6. Springer, Berlin. doi:https://doi.org/10.1007/978-3-642-67778-6
Winn M, Casey E, Habimana O, Murphy CD (2014) Characteristics of Streptomyces griseus biofilms in continuous flow tubular reactors. FEMS Microbiol Lett 352:157–164. https://doi.org/10.1111/1574-6968.12378
Xie Y, Wang B, Liu J, Zhou J, Ma J, Huang H, Ju J (2012) Identification of the biosynthetic gene cluster and regulatory cascade for the synergistic antibacterial antibiotics griseoviridin and viridogrisein in Streptomyces griseoviridis. ChemBioChem 13:2745–2757. https://doi.org/10.1002/cbic.201200584
Yandigeri MS, Malviya N, Solanki MK, Shrivastava P, Sivakumar G (2015) Chitinolytic Streptomyces vinaceusdrappus S5MW2 isolated from Chilika lake, India enhances plant growth and biocontrol efficacy through chitin supplementation against Rhizoctonia solani. World J Microbiol Biotechnol 31:1217–1225. https://doi.org/10.1007/s11274-015-1870-x
Yu J-H, Seipke RF, Barke J, Brearley C, Hill L, Yu DW, Goss RJM, Hutchings MI (2011) A single Streptomyces symbiont makes multiple antifungals to support the fungus farming ant Acromyrmex octospinosus. PLoS One 6. https://doi.org/10.1371/journal.pone.0022028
Yuan WM, Crawford DL (1995) Characterization of Streptomyces lydicus WYEC108 as a potential biocontrol agent against fungal root and seed rots. Appl Environ Microbiol 61:3119–3128
Zappelini C, Alvarez-Lopez V, Capelli N, Guyeux C, Chalot M (2018) Streptomyces dominate the soil under Betula trees that have naturally colonized a red gypsum landfill. Front Microbiol 9. https://doi.org/10.3389/fmicb.2018.01772
Zhang J, Liu J, Meng L, Ma Z, Tang X, Cao Y, Sun L (2012) Isolation and characterization of plant growth-promoting rhizobacteria from wheat roots by wheat germ agglutinin labeled with fluorescein isothiocyanate. J Microbiol 50:191–198. https://doi.org/10.1007/s12275-012-1472-3
Zhao J, Xue Q-H, Shen G-H, Xue L, Duan J-L, Wang D-S (2012) Evaluation of Streptomyces spp. for biocontrol of gummy stem blight (Didymella bryoniae) and growth promotion of Cucumis melo L. Biocontrol Sci Tech 22:23–37. https://doi.org/10.1080/09583157.2011.636481
Zuo L, Jiang B, Jiang Z, Zhao W, Li S, Liu H, Hong B, Yu L, Zuo L, Wu L (2016) Hangtaimycin, a peptide secondary metabolite discovered from Streptomyces spectabilis CPCC 200148 by chemical screening. J Antibiot 69:835–838. https://doi.org/10.1038/ja.2016.29
Acknowledgments
The authors would like to gratefully acknowledge the financial support of the European Regional Development Fund and the regional Ministry of Education of Junta de Castilla y León through project VA258P18, and the European Union funding through project LIFE+ AMMONIA TRAPPING (LIFE15-ENV/ES/000284).
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2020 Springer Nature Switzerland AG
About this chapter
Cite this chapter
Buzón-Durán, L., Pérez-Lebeña, E., Martín-Gil, J., Sánchez-Báscones, M., Martín-Ramos, P. (2020). Applications of Streptomyces spp. Enhanced Compost in Sustainable Agriculture. In: Meghvansi, M., Varma, A. (eds) Biology of Composts. Soil Biology, vol 58. Springer, Cham. https://doi.org/10.1007/978-3-030-39173-7_13
Download citation
DOI: https://doi.org/10.1007/978-3-030-39173-7_13
Published:
Publisher Name: Springer, Cham
Print ISBN: 978-3-030-39172-0
Online ISBN: 978-3-030-39173-7
eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)