참고문헌
- Larkin MJ, Kulakov LA, Allen CC. 2006. Biodegradation by members of the genus Rhodococcus: biochemistry, physiology, and genetic adaptation. Adv. Appl. Microbiol. 59: 1-29.
- Hwang CY, Lee I, Cho Y, Lee YM, Baek K, Jung YJ, et al. 2015. Rhodococcus aerolatus sp. nov., isolated from subarctic rainwater. Int. J. Syst. Evol. Microbiol. 65: 465-471. https://doi.org/10.1099/ijs.0.070086-0
- Goordial J, Raymond-Bouchard I, Zolotarov Y, de Bethencourt L, Ronholm J, Shapiro N, et al. 2016. Cold adaptive traits revealed by comparative genomic analysis of the eurypsychrophile Rhodococcus sp. JG3 isolated from high elevation McMurdo Dry Valley permafrost, Antarctica. FEMS Microbiol. Ecol. 92: fiv154. https://doi.org/10.1093/femsec/fiw154
- Sinha RK, Krishnan KP, Hatha AA, Rahiman M, Thres yamma DD, Kerkar S. 2017. Divers ity of retrievable heterotrophic bacteria in Kongsfjorden, an Arctic fjord. Braz. J. Microbiol. 48: 51-61. https://doi.org/10.1016/j.bjm.2016.09.011
- Martinkova L, Uhnakova B, Patek M, Nesvera J, Kren V. 2009. Biodegradation potential of the genus Rhodococcus. Environ. Int. 35: 162-177. https://doi.org/10.1016/j.envint.2008.07.018
- Larkin MJ, Kulakov LA, Allen CC. 2005. Biodegradation and Rhodococcus - masters of catabolic versatility. Curr. Opin. Biotechnol. 16: 282-290. https://doi.org/10.1016/j.copbio.2005.04.007
- Singh R, Sharma R, Tewari N, Geetanjali, Rawat DS. 2006. Nitrilase and its application as a 'green' catalyst. Chem. Biodivers. 3: 1279-1287. https://doi.org/10.1002/cbdv.200690131
- Kim D, Yoo M, Choi KY, Kang BS, Kim TK, Hong SG, et al. 2011. Differential degradation of bicyclics with aromatic and alicyclic rings by Rhodococcus sp. strain DK17. Appl. Environ. Microbiol. 77: 8280-8287. https://doi.org/10.1128/AEM.06359-11
- Yam KC, Okamoto S, Roberts JN, Eltis LD. 2011. Adventures in Rhodococcus - from steroids to explosives. Can. J. Microbiol. 57: 155-168. https://doi.org/10.1139/W10-115
- Sainsbury PD, Hardiman EM, Ahmad M, Otani H, Seghezzi N, Eltis LD, et al. 2013. Breaking down lignin to high-value chemicals: the conversion of lignocellulose to vanillin in a gene deletion mutant of Rhodococcus jostii RHA1. ACS Chem. Biol. 8: 2151-2156. https://doi.org/10.1021/cb400505a
- Warren R, Hsiao WW, Kudo H, Myhre M, Dosanjh M, Petrescu A, et al. 2004. Functional characterization of a catabolic plasmid from polychlorinated-biphenyl-degrading Rhodococcus sp. strain RHA1. J. Bacteriol. 186: 7783-7795. https://doi.org/10.1128/JB.186.22.7783-7795.2004
- Dabrock B, Kesseler M, Averhoff B, Gottschalk G. 1994. Identification and characterization of a transmissible linear plasmid from Rhodococcus erythropolis BD2 that encodes isopropylbenzene and trichloroethene catabolism. Appl. Environ. Microbiol. 60: 853-860. https://doi.org/10.1128/AEM.60.3.853-860.1994
- Patrauchan MA, Florizone C, Dosanjh M, Mohn WW, Davies J, Eltis LD. 2005. Catabolism of benzoate and phthalate in Rhodococcus sp. strain RHA1: redundancies and convergence. J. Bacteriol. 187: 4050-4063. https://doi.org/10.1128/JB.187.12.4050-4063.2005
- McLeod MP, Warren RL, Hsiao WW, Araki N, Myhre M, Fernandes C, et al. 2006. The complete genome of Rhodococcus sp. RHA1 provides insights into a catabolic powerhouse. Proc. Natl. Acad. Sci. USA 103: 15582-15587. https://doi.org/10.1073/pnas.0607048103
- Choi KY, Kim D, Chae JC, Zylstra GJ, Kim E. 2007. Requirement of duplicated operons for maximal metabolism of phthalate by Rhodococcus sp. strain DK17. Biochem. Biophys. Res. Commun. 357: 766-771. https://doi.org/10.1016/j.bbrc.2007.04.009
- Choi KY, Zylstra GJ, Kim E. 2007. Benzoate catabolite repression of the phthalate degradation pathway in Rhodococcus sp. strain DK17. Appl. Environ. Microbiol. 73: 1370-1374. https://doi.org/10.1128/AEM.02379-06
- Yoo M, Kim D, Choi KY, Chae JC, Zylstra GJ, Kim E. 2012. Draft genome sequence and comparative analysis of the superb aromatic-hydrocarbon degrader Rhodococcus sp. strain DK17. J. Bacteriol. 194: 4440. https://doi.org/10.1128/JB.00844-12
- de Carvalho CC, Cos ta SS, Fernandes P, Couto I, Viveiros M. 2014. Membrane transport systems and the biodegradation potential and pathogenicity of genus Rhodococcus. Front Physiol. 5: 133.
- Maruyama T, Ishikura M, Taki H, Shindo K, Kasai H, Haga M, et al. 2005. Isolation and characterization of o-xylene oxygenase genes from Rhodococcus opacus TKN14. Appl. Environ. Microbiol. 71: 7705-7715. https://doi.org/10.1128/AEM.71.12.7705-7715.2005
- Kim D, Chae JC, Zylstra GJ, Kim YS, Kim SK, Nam MH, et al. 2004. Identification of a novel dioxygenase involved in metabolism of o-xylene, toluene, and ethylbenzene by Rhodococcus sp. strain DK17. Appl. Environ. Microbiol. 70: 7086-7092. https://doi.org/10.1128/AEM.70.12.7086-7092.2004
- Kim D, Chae JC, Zylstra GJ, Sohn HY, Kwon GS, Kim E. 2005. Identification of two-component regulatory genes involved in o-xylene degradation by Rhodococcus sp. strain DK17. J. Microbiol. 43: 49-53.
- Kohyama E, Yoshimura A, Aoshima D, Yoshida T, Kawamoto H, Nagasawa T. 2006. Convenient treatment of acetonitrile-containing wastes using the tandem combination of nitrile hydratase and amidase-producing microorganisms. Appl. Microbiol. Biotechnol. 72: 600-606. https://doi.org/10.1007/s00253-005-0298-x
- Paisio CE, Quevedo MR, Talano MA, Gonzalez PS, Agostini E. 2014. Application of two bacterial strains for wastewater bioremediation and assessment of phenolics biodegradation. Environ. Technol. 35: 1802-1810. https://doi.org/10.1080/09593330.2014.882994
- Jeong E, Hirai M, Shoda M. 2008. Removal of o-xylene using biofilter inoculated with Rhodococcus sp. BTO62. J. Hazard. Mater. 152: 140-147. https://doi.org/10.1016/j.jhazmat.2007.06.078
- Jeong E, Hirai M, Shoda M. 2009. Removal of xylene by a mixed culture of Pseudomonas sp. NBM21 and Rhodococcus sp. BTO62 in biofilter. J. Biosci. Bioeng. 108: 136-141. https://doi.org/10.1016/j.jbiosc.2009.03.024
- Rodrigues JL, Kachel CA, Aiello MR, Quensen JF, Maltseva OV, Tsoi TV, et al. 2006. Degradation of aroclor 1242 dechlorination products in sediments by Burkholderia xenovorans LB400 (ohb) and Rhodococcus sp. strain RHA1 (fcb). Appl. Environ. Microbiol. 72: 2476-2482. https://doi.org/10.1128/AEM.72.4.2476-2482.2006
- Baxter J, Garton NJ, Cummings SP. 2006. The impact of acrylonitrile and bioaugmentation on the biodegradation activity and bacterial community structure of topsoil. Folia Microbiol. 51: 591-597. https://doi.org/10.1007/BF02931624
- Kim D, Park MJ, Koh SC, So JS, Kim E. 2002. Three separate pathways for the initial oxidation of limonene, biphenyl, and phenol by Rhodococcus sp. strain T104. J. Microbiol. 40: 86-89.
- Suttinun O, Muller R, Luepromchai E. 2009. Trichloroethylene cometabolic degradation by Rhodococcus sp. L4 induced with plant essential oils. Biodegradation 20: 281-291. https://doi.org/10.1007/s10532-008-9220-4
- Suttinun O, Muller R, Luepromchai E. 2010. Cometabolic degradation of trichloroethene by Rhodococcus sp. strain L4 immobilized on plant materials rich in essential oils. Appl. Environ. Microbiol. 76: 4684-4690. https://doi.org/10.1128/AEM.03036-09
- Labbe D, Margesin R, Schinner F, Whyte LG, Greer CW. 2007. Comparative phylogenetic analysis of microbial communities in pristine and hydrocarbon-contaminated Alpine soils. FEMS Microbiol. Ecol. 59: 466-475. https://doi.org/10.1111/j.1574-6941.2006.00250.x
- Margesin R. 2007. Alpine microorganisms: useful tools for low-temperature bioremediation. J. Microbiol. 45: 281-285.
- Kim D, Yoo M, Kim E, Hong SG. 2015. Anthranilate degradation by a cold-adapted Pseudomonas sp. J. Basic Microbiol. 55: 354-362. https://doi.org/10.1002/jobm.201300079
- Margesin R, Moertelmaier C, Mair J. 2013. Low-temperature biodegradation of petroleum hydrocarbons (n-alkanes, phenol, anthracene, pyrene) by four actinobacterial strains. Int. Biodeterior. Biodegradation 84: 185-191. https://doi.org/10.1016/j.ibiod.2012.05.004
- Lee GLY, Ahmad SA, Yasid NA, Zulkharnain A, Convey P, Johari WLW, et al. 2018. Biodegradation of phenol by coldadapted bacteria from Antarctic soils. Polar Biol. 41: 553-562. https://doi.org/10.1007/s00300-017-2216-y
- de Carvalho CC, da Fonseca MM. 2005. The remarkable Rhodococcus erythropolis. Appl. Microbiol. Biotechnol. 67: 715-726. https://doi.org/10.1007/s00253-005-1932-3
- Nolan LC, O'Connor KE. 2008. Dioxygenase- and monooxygenase-catalysed synthesis of cis-dihydrodiols, catechols, epoxides and other oxygenated products. Biotechnol. Lett. 30: 1879-1891. https://doi.org/10.1007/s10529-008-9791-5
- Kim D, Yoo M, Choi KY, Kang BS, Kim E. 2013. Characterization and engineering of an o-xylene dioxygenase for biocatalytic applications. Bioresour. Technol. 145: 123-127. https://doi.org/10.1016/j.biortech.2013.03.034
- Priefert H, O'Brien XM, Lessard PA, Dexter AF, Choi EE, Tomic S, et al. 2004. Indene bioconversion by a toluene inducible dioxygenase of Rhodococcus sp. I24. Appl. Microbiol. Biotechnol. 65: 168-176. https://doi.org/10.1007/s00253-004-1589-3
- Pandi-Perumal SR, Srinivasan V, Poeggeler B, Hardeland R, Cardinali DP. 2007. Drug insight: the use of melatonergic agonists for the treatment of insomnia - focus on ramelteon. Nat. Clin. Pract. Neurol. 3: 221-228. https://doi.org/10.1038/ncpneuro0467
- Raj J, Prasad S, Sharma NN, Bhalla TC. 2010. Bioconversion of acrylonitrile to acrylamide using polyacrylamide entrapped cells of Rhodococcus rhodochrous PA-34. Folia Microbiol. 55: 442-446. https://doi.org/10.1007/s12223-010-0074-x
- Kamal A, Kumar MS, Kumar CG, Shaik T. 2011. Bioconversion of acrylonitrile to acrylic acid by Rhodococcus ruber s train AKSH-84. J. Microbiol. Biotechnol. 21: 37-42. https://doi.org/10.4014/jmb.1006.06044
- Sun J, Yu H, Chen J, Luo H, Shen Z. 2016. Ammonium acrylate biomanufacturing by an engineered Rhodococcus ruber with nitrilase overexpression and double-knockout of nitrile hydratase and amidase. J. Ind. Microbiol. Biotechnol. 43: 1631-1639. https://doi.org/10.1007/s10295-016-1840-9
- Zakzeski J, Bruijnincx PC, Jongerius AL, Weckhuysen BM. 2010. The catalytic valorization of lignin for the production of renewable chemicals. Chem. Rev. 110: 3552-3599. https://doi.org/10.1021/cr900354u
- Bugg TDH, Ahmad M, Hardiman EM, Rahmanpour R. 2011. Pathways for degradation of lignin in bacteria and fungi. Nat. Prod. Rep. 28: 1883-1896. https://doi.org/10.1039/c1np00042j
- Gellerstedt G. 2015. Softwood kraft lignin: raw material for the future. Ind. Crops Prod. 77: 845-854. https://doi.org/10.1016/j.indcrop.2015.09.040
- Ahmad M, Roberts JN, Hardiman EM, Singh R, Eltis LD, Bugg TD. 2011. Identification of DypB from Rhodococcus jostii RHA1 as a lignin peroxidase. Biochemistry 50: 5096-5107. https://doi.org/10.1021/bi101892z
- Rahmanpour R, Bugg TD. 2013. Assembly in vitro of Rhodococcus jostii RHA1 encapsulin and peroxidase DypB to form a nanocompartment. FEBS J. 280: 2097-2104. https://doi.org/10.1111/febs.12234
- Bae HW, K im D, Choi KY, Kwon NR, Chae JC, Zyls tra GJ, et al. 2007. Functional identification of p-cumate operons in the terpene-degrading Rhodococcus sp. strain T104. FEMS Microbiol. Lett. 266: 54-59. https://doi.org/10.1111/j.1574-6968.2006.00497.x
- De Carvalho CCCR, Van Keulen F, Da Fonseca MMR. 2000. Biotransformation of limonene-1,2-epoxide to limonene-1,2-diol by Rhodococcus erythropolis cells: an introductory approach to selective hydrolysis and product separation. Food Technol. Biotechnol. 38: 181-185.
- van der Werf MJ, Boot AM. 2000. Metabolism of carveol and dihydrocarveol in Rhodococcus erythropolis DCL14. Microbiology 146: 1129-1141. https://doi.org/10.1099/00221287-146-5-1129
- de Carvalho CC, Poretti A, da Fonseca MM. 2005. Cell adaptation to solvent, substrate and product: a successful strategy to overcome product inhibition in a bioconversion system. Appl. Microbiol. Biotechnol. 69: 268-275. https://doi.org/10.1007/s00253-005-1967-5
- Duetz WA, Fjällman AH, Ren S, Jourdat C, Witholt B. 2001. Biotransformation of D-limonene to (+) trans-carveol by toluene-grown Rhodococcus opacus PWD4 cells. Appl. Environ. Microbiol. 67: 2829-2832. https://doi.org/10.1128/AEM.67.6.2829-2832.2001
-
Thompson ML, Marriott R, Dowle A, Grogan G. 2010. Biotransformation of
${\beta}$ -myrcene to geraniol by a strain of Rhodococcus erythropolis isolated by selective enrichment from hop plants. Appl. Microbiol. Biotechnol. 85: 721-730. https://doi.org/10.1007/s00253-009-2182-6 - Garcia JL, Uhia I, Galan B. 2012. Catabolism and biotechnological applications of cholesterol degrading bacteria. Microb. Biotechnol. 5: 679-699. https://doi.org/10.1111/j.1751-7915.2012.00331.x
-
Yang X, Dubnau E, Smith I, Sampson NS. 2007. Rv1106c from Mycobacterium tuberculosis is a
$3{\beta}$ -hydroxysteroid dehydrogenase. Biochemistry 46: 9058-9067. https://doi.org/10.1021/bi700688x - Van der Geize R, Yam K, Heus er T, Wilbrink MH, Hara H, Anderton MC, et al. 2007. A gene cluster encoding cholesterol catabolism in a soil actinomycete provides insight into Mycobacterium tuberculosis survival in macrophages. Proc. Natl. Acad. Sci. USA 104: 1947-1952. https://doi.org/10.1073/pnas.0605728104
- Fernandes P, Cruz A, Angelova B, Pinheiro HM, Cabral JMS. 2003. Microbial conversion of steroid compounds: recent developments. Enzyme Microb. Technol. 32: 688-705. https://doi.org/10.1016/S0141-0229(03)00029-2
- Sojo MM, Bru RR, Garcia-Carmona FF. 2002. Rhodococcus erythropolis ATCC 25544 as a suitable source of cholesterol oxidase: cell-linked and extracellular enzyme synthesis, purification and concentration. BMC Biotechnol. 2: 3. https://doi.org/10.1186/1472-6750-2-3
- Arora PK, Kumar M, Chauhan A, Raghava GP, Jain RK. 2009. OxDBase: a database of oxygenases involved in biodegradation. BMC Res. Notes 2: 67. https://doi.org/10.1186/1756-0500-2-67
- Carbajosa G, Trigo A, Valencia A, Cases I. 2009. Bionemo: molecular information on biodegradation metabolism. Nucleic Acids Res. 37 (Database issue): D598-D602. https://doi.org/10.1093/nar/gkn864
- Caspi R, Altman T, Dreher K, Fulcher CA, Subhraveti P, Keseler IM, et al. 2012. The MetaCyc database of metabolic pathways and enzymes and the BioCyc collection of pathway/genome databases. Nucleic Acids Res. 40(D1): D742-D753. https://doi.org/10.1093/nar/gkr1014
- Ellis L B, Wackett LP. 2012. Use of the University of Minnesota Biocatalysis/biodegradation Database for study of microbial degradation. Microb. Inform. Exp. 2: 1. https://doi.org/10.1186/2042-5783-2-1
- Kanehisa M. 2013. Chemical and genomic evolution of enzyme-catalyzed reaction networks. FEBS Lett. 587: 2731-2737. https://doi.org/10.1016/j.febslet.2013.06.026
- Fernandez d e Las Heras L, Perera J , Navarro Llorens JM. 2014. Cholesterol to cholestenone oxidation by ChoG, the main extracellular cholesterol oxidase of Rhodococcus ruber strain Chol-4. J. Steroid Biochem. Mol. Biol. 139: 33-44. https://doi.org/10.1016/j.jsbmb.2013.10.001
- Khairy H, Meinert C, Wübbeler JH, Poehlein A, Daniel R, Voigt B, et al. 2016. Genome and proteome analysis of Rhodococcus erythropolis MI2: elucidation of the 4,4'-dithiodibutyric acid catabolism. PLoS One 11: e0167539. https://doi.org/10.1371/journal.pone.0167539
- Arora PK, Bae H. 2014. Integration of bioinformatics to biodegradation. Biol. Proced. Online 16: 8. https://doi.org/10.1186/1480-9222-16-8
- Perez-Pantoja D, De la Iglesia R, Pieper DH, Gonzalez B. 2008. Metabolic reconstruction of aromatic compounds degradation from the genome of the amazing pollutantdegrading bacterium Cupriavidus necator JMP134. FEMS Microbiol. Rev. 32: 736-794. https://doi.org/10.1111/j.1574-6976.2008.00122.x
- Romero-Silva MJ, Mendez V, Agullo L, Seeger M. 2013. Genomic and functional analyses of the gentisate and protocatechuate ring-cleavage pathways and related 3-hydroxybenzoate and 4-hydroxybenzoate peripheral pathways in Burkholderia xenovorans LB400. PLoS One 8: e56038. https://doi.org/10.1371/journal.pone.0056038
- De Santi C, Tedesco P, Ambrosino L, Altermark B, Willassen NP, de Pascale D. 2014. A new alkaliphilic coldactive esterase from the psychrophilic marine bacterium Rhodococcus sp.: functional and structural studies and biotechnological potential. Appl. Biochem. Biotechnol. 172: 3054-3068. https://doi.org/10.1007/s12010-013-0713-1
- Santiago M, Ramirez-Sarmiento CA, Zamora RA, Parra LP. 2016. Discovery, molecular mechanisms, and industrial applications of cold-active enzymes. Front. Microbiol. 7: 1408.
- Nagasawa T, Mathew CD, Mauger J, Yamada H. 1988. Nitrile hydratase-catalyzed production of nicotinamide from 3-cyanopyridine in Rhodococcus rhodochrous J1. Appl. Environ. Microbiol. 54: 1766-1769. https://doi.org/10.1128/AEM.54.7.1766-1769.1988
- Gorlatov SN, Maltseva OV, Shevchenko VI, Golovleva LA. 1989. Degradation of chlorophenols by a culture of Rhodococcus erythropolis. Mikrobiologiya 58: 802-806. [Microbiology 58: 647-651]
-
Bhalla TC, Miura A, Wakamoto A, Ohba Y, Furuhashi K. 1992. Asymmetric hydrolysis of
${\alpha}$ -aminonitriles to optically active amino acids by a nitrilase of Rhodococcus rhodochrous PA-34. Appl. Microbiol. Biotechnol. 37: 184-190. - Chung S Y, M aeda M , Song E, Horikos hi K, Kudo T . 1994. Isolation and characterization of a gram-positive polychlorinated biphenyl-degrading bacterium, Rhodococcus erythropolis s train TA421, from a termite ecosystem. Biosci. Biotechnol. Biochem. 58: 2111-2113. https://doi.org/10.1271/bbb.58.2111
- Blakey AJ, Colby J, Williams E, O'Reilly C. 1995. Regio- and stereo-specific nitrile hydrolysis by the nitrile hydratase from Rhodococcus AJ270. FEMS Microbiol. Lett. 129: 57-62.
- Masai E, Yamada A, Healy JM, Hatta T, Kimbara K, Fukuda M, et al. 1995. Characterization of biphenyl catabolic genes of gram-positive polychlorinated biphenyl degrader Rhodococcus sp. strain RHA1. Appl. Environ. Microbiol. 61: 2079-2085.
- Hernandez BS, Koh SC, Chial M, Focht DD. 1997. Terpeneutilizing isolates and their relevance to enhanced biotransformation of polychlorinated biphenyls in soil. Biodegradation 8: 153-158. https://doi.org/10.1023/A:1008255218432
- Chartrain M, Jackey B, Taylor C, Sandford V, Gbewonyo K, Lister L, et al. 1998. Bioconversion of indene to cis (1S,2R) indandiol and trans (1R,2R) indandiol by Rhodococcus species. J. Ferment. Bioeng. 86: 550-558. https://doi.org/10.1016/S0922-338X(99)80005-1
- Yakimov MM, Giuliano L, Bruni V, Scarfì S, Golyshin PN. 1999. Characterization of Antarctic hydrocarbon-degrading bacteria capable of producing bioemulsifiers. New Microbiol. 22: 249-256.
- Kim D, Kim YS, Kim SK, Kim SW, Zylstra GJ, Kim YM, et al. 2002. Monocyclic aromatic hydrocarbon degradation by Rhodococcus sp. strain DK17. Appl. Environ. Microbiol. 68: 3270-3278. https://doi.org/10.1128/AEM.68.7.3270-3278.2002
- Margesin R, Fonteyne PA, Redl B. 2005. Low-temperature biodegradation of high amounts of phenol by Rhodococcus spp. and basidiomycetous yeasts. Res. Microbiol. 156: 68-75. https://doi.org/10.1016/j.resmic.2004.08.002
- Na KS, Kuroda A, Takiguchi N, Ikeda T, Ohtake H, Kato J. 2005. Isolation and characterization of benzene-tolerant Rhodococcus opacus strains. J. Biosci. Bioeng. 99: 378-382. https://doi.org/10.1263/jbb.99.378
- Sekine M, Tanikawa S, Omata S, Saito M, Fujisawa T, Tsukatani N, et al. 2006. Sequence analysis of three plasmids harboured in Rhodococcus erythropolis strain PR4. Environ. Microbiol. 8: 334-346. https://doi.org/10.1111/j.1462-2920.2005.00899.x
- Ma Y, Yu H, Pan W, Liu C, Zhang S, Shen Z. 2010. Identification of nitrile hydratase-producing Rhodococcus ruber TH and characterization of an amiE-negative mutant. Bioresour. Technol. 101: 285-291. https://doi.org/10.1016/j.biortech.2009.07.057
- Cai Q, Zhang B, Chen B, Zhu Z, Lin W, Cao T. 2014. Screening of biosurfactant producers from petroleum hydrocarbon contaminated sources in cold marine environments. Mar. Pollut. Bull. 86: 402-410. https://doi.org/10.1016/j.marpolbul.2014.06.039
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