A Novel Bioflocculant Produced by Cobetia marina MCCC1113: Optimization of Fermentation Conditions by Response Surface Methodology and Evaluation of Flocculation Performance when Harvesting Microalgae
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Bérdy J. Bioactive microbial metabolites. J Antibiot. 2005 Jan; 58(1): 1–26. https://doi.org/10.1038/ja.2005.1BérdyJBioactive microbial metabolites2005Jan581126https://doi.org/10.1038/ja.2005.110.1038/ja.2005.115813176Search in Google Scholar
Cerff M, Morweiser M, Dillschneider R, Michel A, Menzel K, Posten C. Harvesting fresh water and marine algae by magnetic separation: Screening of separation parameters and high gradient magnetic filtration. Bioresour Technol. 2012 Aug;118:289–295. https://doi.org/10.1016/j.biortech.2012.05.020CerffMMorweiserMDillschneiderRMichelAMenzelKPostenCHarvesting fresh water and marine algae by magnetic separation: Screening of separation parameters and high gradient magnetic filtration2012Aug118289295https://doi.org/10.1016/j.biortech.2012.05.02010.1016/j.biortech.2012.05.02022705536Search in Google Scholar
Chang YI, Su CY. Flocculation behavior of Sphingobium chlorophenolicum in degrading pentachlorophenol at different life stages. Biotechnol Bioeng. 2003 Jun 30;82(7):843–850. https://doi.org/10.1002/bit.10634ChangYISuCYFlocculation behavior of Sphingobium chlorophenolicum in degrading pentachlorophenol at different life stages2003Jun 30827843850https://doi.org/10.1002/bit.1063410.1002/bit.1063412701151Search in Google Scholar
Christenson L, Sims R. Production and harvesting of microalgae for wastewater treatment, biofuels, and bioproducts. Biotechnol Adv. 2011 Nov–Dec;29(6):686–702. https://doi.org/10.1016/j.biotechadv.2011.05.015ChristensonLSimsRProduction and harvesting of microalgae for wastewater treatment, biofuels, and bioproducts2011Nov–Dec296686702https://doi.org/10.1016/j.biotechadv.2011.05.01510.1016/j.biotechadv.2011.05.01521664266Search in Google Scholar
Colonia BSO, de Melo Pereira GV, Mendonça Rodrigues F, de Souza Miranda Muynarsk E, da Silva Vale A, Cesar de Carvalho J, Thomaz Soccol V, de Oliveira Penha R, Ricardo Soccol C. Integrating metagenetics and high-throughput screening for bioprospecting marine thraustochytrids producers of long-chain polyunsaturated fatty acids. Bioresour Technol. 2021 Aug;333:125176. http://doi.org/10.1016/j.biortech.2021.125176ColoniaBSOdeMelo Pereira GVMendonçaRodrigues FdeSouza Miranda Muynarsk EdaSilva Vale ACesarde Carvalho JThomazSoccol VdeOliveira Penha RRicardoSoccol CIntegrating metagenetics and high-throughput screening for bioprospecting marine thraustochytrids producers of long-chain polyunsaturated fatty acids2021Aug333125176http://doi.org/10.1016/j.biortech.2021.12517610.1016/j.biortech.2021.12517633894449Search in Google Scholar
Cosa S, Mabinya LV, Olaniran AO, Okoh OO, Bernard K, Deyzel S, Okoh AI. Bioflocculant production by Virgibacillus sp. Rob isolated from the bottom sediment of Algoa Bay in the Eastern Cape, South Africa. Molecules. 2011 Mar 14;16(3):2431–2442. https://doi.org/10.3390/molecules16032431CosaSMabinyaLVOlaniranAOOkohOOBernardKDeyzelSOkohAIBioflocculant production by Virgibacillus sp2011Mar 1416324312442https://doi.org/10.3390/molecules1603243110.3390/molecules16032431625963621403600Search in Google Scholar
Garcia BB, Lourinho G, Romano P, Brito PSD. Photocatalytic degradation of swine wastewater on aqueous TiO2 suspensions: optimization and modeling via Box-Behnken design. Heliyon. 2020; 6(1): e03293. https://doi.org/10.1016/j.heliyon.2020.e03293GarciaBBLourinhoGRomanoPBritoPSDPhotocatalytic degradation of swine wastewater on aqueous TiO2 suspensions: optimization and modeling via Box-Behnken design202061e03293https://doi.org/10.1016/j.heliyon.2020.e0329310.1016/j.heliyon.2020.e03293700286132051866Search in Google Scholar
Gong WX, Wang SG, Sun XF, Liu XW, Yue QY, Gao BY. Bioflocculant production by culture of Serratia ficaria and its application in wastewater treatment. Bioresour Technol. 2008 Jul;99(11):4668–4674. http://doi.org/10.1016/j.biortech.2007.09.077GongWXWangSGSunXFLiuXWYueQYGaoBYBioflocculant production by culture of Serratia ficaria and its application in wastewater treatment2008Jul991146684674http://doi.org/10.1016/j.biortech.2007.09.07710.1016/j.biortech.2007.09.07718024024Search in Google Scholar
Haider MA, Pakshirajan K. Screening and optimization of media constituents for enhancing lipolytic activity by a soil microorganism using statistically designed experiments. Appl Biochem Biotechnol. 2007 May–Jun;141(2–3): 377–390. http://doi.org/10.1007/BF02729074HaiderMAPakshirajanKScreening and optimization of media constituents for enhancing lipolytic activity by a soil microorganism using statistically designed experiments2007May–Jun1412–3377390http://doi.org/10.1007/BF0272907410.1007/BF0272907418025563Search in Google Scholar
Hubbard AT. Encyclopedia of Surface and Colloid Science; CRC Press: Boca Raton, FL, USA, 2004; p. 4230.HubbardATCRC PressBoca Raton, FL, USA2004p4230Search in Google Scholar
Jeganathan PM, Venkatachalam S, Karichappan T, Ramasamy S. Model development and process optimization for solvent extraction of polyphenols from red grapes using Box-Behnken design. Prep Biochem Biotechnol. 2014;44(1):56–67. http://doi.org/10.1080/10826068.2013.791629JeganathanPMVenkatachalamSKarichappanTRamasamySModel development and process optimization for solvent extraction of polyphenols from red grapes using Box-Behnken design20144415667http://doi.org/10.1080/10826068.2013.79162910.1080/10826068.2013.79162924117152Search in Google Scholar
Juarez Tomás MS, Bru E, Wiese B, de Ruiz Holgado AA, Nader-Macías ME. Influence of pH, temperature and culture media on the growth and bacteriocin production by vaginal Lactobacillus salivarius CRL 1328. J Appl Microbiol. 2002;93(4):714–724. https://doi.org/10.1046/j.1365-2672.2002.01753.xJuarezTomás MSBruEWieseBdeRuiz Holgado AANader-MacíasMEInfluence of pH, temperature and culture media on the growth and bacteriocin production by vaginal Lactobacillus salivarius CRL 13282002934714724https://doi.org/10.1046/j.1365-2672.2002.01753.x10.1046/j.1365-2672.2002.01753.xSearch in Google Scholar
Lachhwani P. Studies on polymeric bioflocculant producing microorganisms [Master Thesis]. Patiala (India): Thapar Institute of Engineering and Technology; 2005.LachhwaniPPatiala (India)Thapar Institute of Engineering and Technology;2005Search in Google Scholar
Lei X, Chen Y, Shao Z, Chen Z, Li Y, Zhu H, Zhang J, Zheng W, Zheng T. Effective harvesting of the microalgae Chlorella vulgaris via flocculation-flotation with bioflocculant. Bioresour Technol. 2015 Dec; 198:922–25. http://doi.org/10.1016/j.biortech.2015.08.095LeiXChenYShaoZChenZLiYZhuHZhangJZhengWZhengTEffective harvesting of the microalgae Chlorella vulgaris via flocculation-flotation with bioflocculant2015Dec19892225http://doi.org/10.1016/j.biortech.2015.08.09510.1016/j.biortech.2015.08.095Search in Google Scholar
Li H, Huang L, Zhang Y, Yan Y. Production, characterization and immunomodulatory activity of an extracellular polysaccharide from Rhodotorula Mucilaginosa Yl-1 isolated from sea salt field Mar Drugs. 2020 Nov 26;18(12):595. http://doi.org/10.3390/md18120595LiHHuangLZhangYYanYProduction, characterization and immunomodulatory activity of an extracellular polysaccharide from Rhodotorula Mucilaginosa Yl-1 isolated from sea salt field2020Nov 261812595http://doi.org/10.3390/md1812059510.3390/md18120595Search in Google Scholar
Li Y, Xu Y, Liu L, Jiang X, Zhang K, Zheng T, Wang H. First evidence of bioflocculant from Shinella albus with flocculation activity on harvesting of Chlorella vulgaris biomass. Bioresour Technol. 2016 Oct;218:807–815. https://doi.org/10.1016/j.biortech.2016.07.034LiYXuYLiuLJiangXZhangKZhengTWangHFirst evidence of bioflocculant from Shinella albus with flocculation activity on harvesting of Chlorella vulgaris biomass2016Oct218807815https://doi.org/10.1016/j.biortech.2016.07.03410.1016/j.biortech.2016.07.034Search in Google Scholar
Lian B, Chen Y, Zhao J, Teng HH, Zhu L, Yuan S Microbial flocculation by Bacillus mucilaginosus: Applications and mechanisms. Bioresour Technol. 2008 Jul;99(11):4825–4831. http://doi.org/10.1016/j.biortech.2007.09.045LianBChenYZhaoJTengHHZhuLYuanSMicrobial flocculation by Bacillus mucilaginosus: Applications and mechanisms2008Jul991148254831http://doi.org/10.1016/j.biortech.2007.09.04510.1016/j.biortech.2007.09.045Search in Google Scholar
Liu LF, Cheng W. Characteristics and culture conditions of a bioflocculant produced by Penicillium sp. Biomed Environ Sci. 2010 Jun;23(3):213–218. http://doi.org/10.1016/S0895-3988(10)60055-4LiuLFChengWCharacteristics and culture conditions of a bioflocculant produced by Penicillium sp2010Jun233213218http://doi.org/10.1016/S0895-3988(10)60055-410.1016/S0895-3988(10)60055-4Search in Google Scholar
Liu W, Wang K, Li B, Yuan H, Yang J. Production and characterization of an intracellular bioflocculant by Chryseobacterium daeguense W6 cultured in low nutrition medium. Bioresour Technol. 2010 Feb; 101(3):1044–1048. http://doi.org/10.1016/j.biortech.2009.08.108LiuWWangKLiBYuanHYangJProduction and characterization of an intracellular bioflocculant by Chryseobacterium daeguense W6 cultured in low nutrition medium2010Feb101310441048http://doi.org/10.1016/j.biortech.2009.08.10810.1016/j.biortech.2009.08.10819766490Search in Google Scholar
Ma R, Wang B, Chua ET, Zhao X, Lu K, Ho SH, Shi X, Liu L, Xie Y, Lu Y, et al. Comprehensive utilization of marine microalgae for enhanced co-production of multiple compounds. Mar Drugs. 2020 Sep 16;18(9):467. http://doi.org/10.3390/md18090467MaRWangBChuaETZhaoXLuKHoSHShiXLiuLXieYLuYet alComprehensive utilization of marine microalgae for enhanced co-production of multiple compounds2020Sep 16189467http://doi.org/10.3390/md1809046710.3390/md18090467755182832948074Search in Google Scholar
Mabinya LV, Cosa S, Mkwetshana N, Okoh AI. Halomonas sp. OKOH – a marine bacterium isolated from the bottom sediment of Algoa Bay – produces a polysaccharide bioflocculant: Partial characterization and biochemical analysis of its properties. Molecules. 2011 May 25;16(6): 4358–4370. http://doi.org/10.3390/molecules16064358MabinyaLVCosaSMkwetshanaNOkohAIHalomonas sp2011May 2516643584370http://doi.org/10.3390/molecules1606435810.3390/molecules16064358626456321613977Search in Google Scholar
Miller GL. Use of dinitrosalicylic acid reagent for determination of reducing sugar. Anal Chem 1959;31(3):426–428. https://doi.org/10.1021/ac60147a030MillerGLUse of dinitrosalicylic acid reagent for determination of reducing sugar1959313426428https://doi.org/10.1021/ac60147a03010.1021/ac60147a030Search in Google Scholar
Moradinejad S, Vandamme D, Glover CM, Seighalani TZ, Zamyadi A. Mini-hydrocyclone separation of cyanobacterial and green algae: Impact on cell viability and chlorine consumption. Water. 2019;11(7):1473. https://doi.org/10.3390/w11071473MoradinejadSVandammeDGloverCMSeighalaniTZZamyadiAMini-hydrocyclone separation of cyanobacterial and green algae: Impact on cell viability and chlorine consumption20191171473https://doi.org/10.3390/w1107147310.3390/w11071473Search in Google Scholar
Al-Rikabey MN, Al-Mayah AM. Cultivation of Chlorella Vulgaris in BG-11 media using Taguchi method. J Adv Res Dyn Control Syst. 2018;10(7):19–30.Al-RikabeyMNAl-MayahAMCultivation of Chlorella Vulgaris in BG-11 media using Taguchi method20181071930Search in Google Scholar
Nontembiso P, Sekelwa C, Leonard MV, Anthony OI. Assessment of bioflocculant production by Bacillus sp. Gilbert, a marine bacterium isolated from the bottom sediment of Algoa Bay. Mar Drugs. 2011;9(7): 1232–1242. https://doi.org/10.3390/md9071232NontembisoPSekelwaCLeonardMVAnthonyOIAssessment of bioflocculant production by Bacillus sp20119712321242https://doi.org/10.3390/md907123210.3390/md9071232314850021822413Search in Google Scholar
Peng F, Liu Z, Wang L, Shao Z. An oil-degrading bacterium: Rhodococcus erythropolis strain 3C-9 and its biosurfactants. J Appl Micro-biol. 2007 Jun;102(6):1603–1611. https://doi.org/10.1111/j.1365-2672.2006.03267.xPengFLiuZWangLShaoZAn oil-degrading bacterium: Rhodococcus erythropolis strain 3C-9 and its biosurfactants2007Jun102616031611https://doi.org/10.1111/j.1365-2672.2006.03267.x10.1111/j.1365-2672.2006.03267.x17578426Search in Google Scholar
Picciotto S, Barone ME, Fierli D, Aranyos A, Adamo G, Božič D, Romancino DP, Stanly C, Parkes R, Morsbach S, et al. Isolation of extracellular vesicles from microalgae: towards the production of sustainable and natural nanocarriers of bioactive compounds. Biomater Sci. 2021 Apr 21;9(8): 2917–2930. https://doi.org/10.1039/d0bm01696aPicciottoSBaroneMEFierliDAranyosAAdamoGBožičDRomancinoDPStanlyCParkesRMorsbachSet alIsolation of extracellular vesicles from microalgae: towards the production of sustainable and natural nanocarriers of bioactive compounds2021Apr 219829172930https://doi.org/10.1039/d0bm01696a10.1039/D0BM01696ASearch in Google Scholar
Romanenko LA, Kurilenko VV, Guzev KV, Svetashev VI. Characterization of Labrenzia polysiphoniae sp. nov. isolated from red alga Polysiphonia sp. Arch Microbiol. 2019 Jul;201(5):705–712. https://doi.org/10.1007/s00203-019-01640-0RomanenkoLAKurilenkoVVGuzevKVSvetashevVICharacterization of Labrenzia polysiphoniae sp2019Jul2015705712https://doi.org/10.1007/s00203-019-01640-010.1007/s00203-019-01640-030810769Search in Google Scholar
Shea C, Nunley JW, Williamson JC, Smith-Somerville HE. Comparison of the adhesion properties of Deleya marina and the exopolysaccharide-defective mutant strain DMR. Appl Environ Microbiol. 1991 Nov;57(11):3107–3113. https://doi.org/10.1128/aem.57.11.3107-3113.1991SheaCNunleyJWWilliamsonJCSmith-SomervilleHEComparison of the adhesion properties of Deleya marina and the exopolysaccharide-defective mutant strain DMR1991Nov571131073113https://doi.org/10.1128/aem.57.11.3107-3113.199110.1128/aem.57.11.3107-3113.19911839341781675Search in Google Scholar
Sun PF, Lin H, Wang G, Lu LL, Zhao YH. Preparation of a new-style composite containing a key bioflocculant produced by Pseudomonas aeruginosa ZJU1 and its flocculating effect on harmful algal blooms. J Hazard Mater. 2015 Mar 2;284:215–221. https://doi.org/10.1016/j.jhazmat.2014.11.025SunPFLinHWangGLuLLZhaoYHPreparation of a new-style composite containing a key bioflocculant produced by Pseudomonas aeruginosa ZJU1 and its flocculating effect on harmful algal blooms2015Mar 2284215221https://doi.org/10.1016/j.jhazmat.2014.11.02510.1016/j.jhazmat.2014.11.02525463236Search in Google Scholar
Ugbenyen A, Cosa S, Mabinya L, Babalola OO, Aghdasi F, Okoh A. Thermostable bacterial bioflocculant produced by Cobetia spp. isolated from Algoa Bay (South Africa). Int J Environ Res Public Health. 2012 Jun;9(6):2108–2120. https://doi.org/10.3390/ijerph9062108UgbenyenACosaSMabinyaLBabalolaOOAghdasiFOkohAThermostable bacterial bioflocculant produced by Cobetia spp2012Jun9621082120https://doi.org/10.3390/ijerph906210810.3390/ijerph9062108339736722829793Search in Google Scholar
Ugbenyen AM, Okoh AI. Characteristics of a bioflocculant produced by a consortium of Cobetia and Bacillus species and its application in the treatment of wastewaters. Water SA. 2014;40(1):139–144. https://doi.org/10.4314/wsa.v40i1.17UgbenyenAMOkohAICharacteristics of a bioflocculant produced by a consortium of Cobetia and Bacillus species and its application in the treatment of wastewaters2014401139144https://doi.org/10.4314/wsa.v40i1.1710.4314/wsa.v40i1.17Search in Google Scholar
Wang L, Ma F, Lee DJ, Wang A, Ren N. Bioflocculants from hydrolysates of corn stover using isolated strain Ochrobactium ciceri W2. Bioresour Technol. 2013 Oct;145:259–263. http://doi.org/10.1016/j.biortech.2012.11.020WangLMaFLeeDJWangARenNBioflocculants from hydrolysates of corn stover using isolated strain Ochrobactium ciceri W22013Oct145259263http://doi.org/10.1016/j.biortech.2012.11.02010.1016/j.biortech.2012.11.02023232033Search in Google Scholar
Xia S, Zhang Z, Wang X, Yang A, Chen L, Zhao J, Leonard D, Jaffrezic-Renault N. Production and characterization of a bioflocculant by Proteus mirabilis TJ-1. Bioresour Technol. 2008 Sep;99(14): 6520–6527. http://doi.org/10.1016/j.biortech.2007.11.031XiaSZhangZWangXYangAChenLZhaoJLeonardDJaffrezic-RenaultNProduction and characterization of a bioflocculant by Proteus mirabilis TJ-12008Sep991465206527http://doi.org/10.1016/j.biortech.2007.11.03110.1016/j.biortech.2007.11.031Search in Google Scholar
Xie Y, Li J, Ho SH, Ma R, Shi X, Liu L, Chen J. Pilot-scale cultivation of Chlorella sorokiniana FZU60 with a mixotrophy/photoautotrophy two-stage strategy for efficient lutein production. Bioresour Technol. 2020 Oct;314:123767. http://doi.org/10.1016/j.biortech.2020.123767XieYLiJHoSHMaRShiXLiuLChenJPilot-scale cultivation of Chlorella sorokiniana FZU60 with a mixotrophy/photoautotrophy two-stage strategy for efficient lutein production2020Oct314123767http://doi.org/10.1016/j.biortech.2020.12376710.1016/j.biortech.2020.123767Search in Google Scholar
Yokoh H, Arima T, Hirose J, Hayashi S, Takaski Y. Flocculation properties of poly (γ-glutamic acid) produced by Bacillus subtilis. J Ferment Bioeng. 1996;82(1):84–88. https://doi.org/10.1016/0922-338X(96)89461-xYokohHArimaTHiroseJHayashiSTakaskiYFlocculation properties of poly (γ-glutamic acid) produced by Bacillus subtilis19968218488https://doi.org/10.1016/0922-338X(96)89461-x10.1016/0922-338X(96)89461-XSearch in Google Scholar
Yuan T, Li XK, Xiao SY, Yuan ZH. Microalgae pretreatment with liquid hot water to enhance enzymatic hydrolysis efficiency. Bioresour Technol. 2016;220:530–536. https://doi.org/10.1016/j.biortech.2016.08.117YuanTLiXKXiaoSYYuanZHMicroalgae pretreatment with liquid hot water to enhance enzymatic hydrolysis efficiency2016220530536https://doi.org/10.1016/j.biortech.2016.08.11710.1016/j.biortech.2016.08.11727614155Search in Google Scholar
Zheng Y, Ye ZL, Fang XL, Li YH, Cai WM. Production and characteristics of a bioflocculant produced by Bacillus sp. F19. Bioresour Technol. 2008 Nov;99(16):7686–7691. https://doi.org/10.1016/j.biortech.2008.01.068ZhengYYeZLFangXLLiYHCaiWMProduction and characteristics of a bioflocculant produced by Bacillus sp2008Nov991676867691https://doi.org/10.1016/j.biortech.2008.01.06810.1016/j.biortech.2008.01.06818358717Search in Google Scholar