참고문헌
- Levasseur W, Perre P, Pozzobon V. 2020. A review of high value-added molecules production by microalgae in light of the classification. Biotechnol. Adv. 41: 107545. https://doi.org/10.1016/j.biotechadv.2020.107545
- Minhas AK, Hodgson P, Barrow CJ, Adholeya A. 2016. A Review on the assessment of stress conditions for simultaneous production of microalgal lipids and carotenoids Front. Microbiol. 7: 546. https://doi.org/10.3389/fmicb.2016.00546
- Markou G, Nerantzis E. 2013. Microalgae for high-value compounds and biofuels production: a review with focus on cultivation under stress conditions. Biotechnol. Adv. 31: 1532-1542. https://doi.org/10.1016/j.biotechadv.2013.07.011
- Bellou S, Baeshen MN, Elazzazy AM, Aggeli D, Sayegh F, Aggelis G. 2014. Microalgal lipids biochemistry and biotechnological perspectives. Biotechnol. Adv. 32: 1476-1493. https://doi.org/10.1016/j.biotechadv.2014.10.003
- Liang MH, Wang L, Wang Q, Zhu J, Jiang JG. High-value bioproducts from microalgae: Strategies and progress. Crit. Rev. Food Sci. Nutr. 59: 2423-2441. https://doi.org/10.1080/10408398.2018.1455030
- Sun H, Zhao W, Mao X, Li Y, Wu T, Chen F. 2018. High-value biomass from microalgae production platforms: strategies and progress based on carbon metabolism and energy conversion. Biotechnol. Biofuels 11: 227. https://doi.org/10.1186/s13068-018-1225-6
- Martinez-Hernandez GB, Castillejo N, Carrion-Monteagudo MDM, Artes F, Artes-Hernandez F. 2018. Nutritional and bioactive compounds of commercialized algae powders used as food supplements. Food Sci. Technol. Int. 24: 172-182. https://doi.org/10.1177/1082013217740000
- Ramos GJP, Bicudo C, do N. Moura CW. 2015. Oocystis apicurvata sp. nov. (Oocystaceae, Trebouxiophyceae), a new species of green algae from Chapada Diamantina, northeast Brazil. Braz. J. Bot. 38: 171-173. https://doi.org/10.1007/s40415-014-0118-6
- Dunker S, Althammer J, Pohnert G, Wilhelm C, Fateful A. 2017. Meeting of two phytoplankton species-chemical vs. cell-cell-interactions in co-cultures of the green algae Oocystis marsonii and the cyanobacterium Microcystis aeruginosa. Microb. Ecol. 74: 22-32. https://doi.org/10.1007/s00248-016-0927-1
- Hepperle D, Hegewald E, Krienitz L. 2000. Phylogenetic position of the Oocystaceae (Chlorophyta). J. Phycol. 36: 590-595. https://doi.org/10.1046/j.1529-8817.2000.99184.x
- Wang X, Zhang Y, Li C, Huang X, Li F, Wang X, Li G. 2020. Allelopathic effect of Oocystis borgei culture on Microcystis aeruginosa. Environ. Technol. 1-10.
- Soldo D, Hari R, Sigg L, Behra R. 2005. Tolerance of Oocystis nephrocytioides to copper: intracellular distribution and extracellular complexation of copper. Aquat. Toxicol. 71: 307-317. https://doi.org/10.1016/j.aquatox.2004.11.011
- Huang X, Li X, Wang Y, Zhou M. 2012. Effects of environmental factors on the uptake rates of dissolved nitrogen by a salt-water green alga (Oocystis borgei Snow). Bull. Environ. Contam. Toxicol. 89: 905-909. https://doi.org/10.1007/s00128-012-0767-8
- Foerster JW. 1971. Environmentally induced morphological changes in Oocystis lacustris (?) Chodat (Chlorophyta). Bull. Torrey Bot. Club. 98: 225-227. https://doi.org/10.2307/2483691
- Liu M, Huang XH, Li CL, Gu B. 2020. Study on the uptake of dissolved nitrogen by Oocystis borgei in prawn (Litopenaeus vannamei) aquaculture ponds and establishment of uptake model. Aquac. Int. 28: 1445-1458. https://doi.org/10.1007/s10499-020-00534-z
- El-Naggar NEA, Hamouda RA, Rabei NH, Mousa IE, Abdel-Hamid MS. 2019. Phycoremediation of lithium ions from aqueous solutions using free and immobilized freshwater green alga Oocystis solitaria: mathematical modeling for bioprocess optimization. Environ. Sci. Pollut. Res. 26: 19335-19351. https://doi.org/10.1007/s11356-019-05214-x
- Xia S, Gao B, Fu J, Xiong J, Zhang C. 2018. Production of fucoxanthin, chrysolaminarin, and eicosapentaenoic acid by Odontella aurita under different nitrogen supply regimes. J. Biosci. Bioeng. 126: 723-729. https://doi.org/10.1016/j.jbiosc.2018.06.002
- Cao M, Wang S, Gao Y, Pan X, Wang X, Deng R, et al. 2020. Study on physicochemical properties and antioxidant activity of polysaccharides from Desmodesmus armatus. J. Food Biochem. 44: e13243.
- Jones J, Allam B, Espinosa EP. 2020. Particle selection in suspension-feeding bivalves: Does one model fit all? Biol. Bull. 238: 41-53. https://doi.org/10.1086/707718
- Mun S. 2018. Optimization of production rate, productivity, and product concentration for a simulated moving bed process aimed atfucose separation using standing-wave-design and genetic algorithm. J. Chromatogr. A 1575: 113-121. https://doi.org/10.1016/j.chroma.2018.09.025
- Jeon YJ, Wijesinghe WA, Kim SK. 2011. Functional properties of brown algal sulfated polysaccharides, fucoidans. Adv. Food Nutr. Res. 64: 163-78. https://doi.org/10.1016/B978-0-12-387669-0.00012-0
- Schultz-Johansen M, Cueff M, Hardouin K, Jam M, Larocque R,Glaring RMA, et al. 2018. Discovery and screening of novel metagenome-derived GH107 enzymes targeting sulfated fucans from brown algae. FEBS J. 285: 4281-4295. https://doi.org/10.1111/febs.14662
- Nunes C, Coimbra MA. 2019. The Potential of fucose-containing sulfated polysaccharides as scaffolds for biomedical applications. Curr. Med. Chem. 26: 6399-6411. https://doi.org/10.2174/0929867326666181213093718
- Ngo DH, Kim SK. 2013. Sulfated polysaccharides as bioactive agents from marine algae. Int. J. Biol. Macromol. 62: 70-75. https://doi.org/10.1016/j.ijbiomac.2013.08.036
- Kim SH, Sunwoo IY, Hong HJ, Awah CC, Jeong GT, Kim SK. 2019. Lipid and unsaturated fatty acid productions from three microalgae using nitrate and light-emitting diodes with complementary LED wavelength in a two-phase culture system. Bioprocess Biosyst. Eng. 42: 1517-1526. https://doi.org/10.1007/s00449-019-02149-y
- Xie D, Jackson EN, Zhu Q. 2015. Sustainable source of omega-3 eicosapentaenoic acid from metabolically engineered Yarrowia lipolytica: from fundamental research to commercial production. Appl. Microbiol. Biotechnol. 99: 1599-1610. https://doi.org/10.1007/s00253-014-6318-y
- Ghasemi Fard S, Wang F, Sinclair AJ, Elliott G, Turchini GM. 2019. How does high DHA fish oil affect health? A systematic review of evidence. Crit. Rev. Food Sci. Nutr. 59:1684-1727. https://doi.org/10.1080/10408398.2018.1425978
- Wen ZY, Chen F. 2003. Heterotrophic production of eicosapentaenoic acid by microalgae, Biotechnol. Adv. 21: 273-294. https://doi.org/10.1016/S0734-9750(03)00051-X
- Aussant J, Guiheneuf F, Stengel DB. 2018. Impact of temperature on fatty acid composition and nutritional value in eight species of microalgae. Appl. Microbiol. Biotechnol. 102: 5279-5297. https://doi.org/10.1007/s00253-018-9001-x
- Zhao Y, Wang HP, Han B, Yu X. 2019. Coupling of abiotic stresses and phytohormones for the production of lipids and high-value by-products by microalgae: A review. Bioresour. Technol. 274: 549-556. https://doi.org/10.1016/j.biortech.2018.12.030
- Yang R, Wei D, Xie J. 2020. Diatoms as cell factories for high-value products: chrysolaminarin, eicosapentaenoic acid, and fucoxanthin. Crit. Rev. Biotechnol. 40: 993-1009. https://doi.org/10.1080/07388551.2020.1805402
- Santos CA, Reis A. 2014. Microalgal symbiosis in biotechnology. Appl. Microbiol. Biotechnol. 98: 5839-5846. https://doi.org/10.1007/s00253-014-5764-x
- Lutzu GA, Turgut Dunford N. 2018 Interactions of microalgae and other microorganisms for enhanced production of high-value compounds. Front. Biosci. (Landmark Ed) 23: 1487-1504. https://doi.org/10.2741/4656
- Cooper NB, Smith AG. 2015. Exploring mutualistic interactions between microalgae and bacteria in the omics age. Curr. Opin. Plant Biol. 26: 147-153. https://doi.org/10.1016/j.pbi.2015.07.003
- Cho DH, Ramanan R, Heo J, Lee J, Kim BH, Oh HM, et al. 2015. Enhancing microalgal biomass productivity by engineering a microalgal-bacterial community. Bioresour. Technol. 175: 578-585. https://doi.org/10.1016/j.biortech.2014.10.159
- Perera I, Subashchandrabose SR, Venkateswarlu K, Naidu R, Megharaj M. 2018. Consortia of cyanobacteria/microalgae and bacteria in desert soils: an underexplored microbiota. Appl. Microbiol. Biotechnol. 102: 7351-7363. https://doi.org/10.1007/s00253-018-9192-1
- Rossi S, Bellucci M, Marazzi F, Mezzanotte V, Ficara E. 2018. Activity assessment of microalgal-bacterial consortia based on respirometric tests. Water Sci. Technol. 78: 207-215. https://doi.org/10.2166/wst.2018.078
- Solimeno A, Parker L, Lundquist T, Garcia J. 2017. Integral microalgae-bacteria model (BIO_ALGAE): Application to wastewater high rate algal ponds. Sci. Total Environ. 601-602: 646-657. https://doi.org/10.1016/j.scitotenv.2017.05.215
- Yao S, Lyu S, An Y, Lu J, Gjermansen C, Schramm A. 2019. Microalgae-bacteria symbiosis in microalgal growth and biofuel production: a review. J. Appl. Microbiol. 126: 359-368. https://doi.org/10.1111/jam.14095
- Meza B, de-Bashan LE, Hernandez JP, Bashan Y. 2015. Accumulation of intra-cellular polyphosphate in Chlorella vulgaris cells is related to indole-3-acetic acid produced by Azospirillum brasilense. Res. Microbiol. 166: 399-407. https://doi.org/10.1016/j.resmic.2015.03.001
- Tandon P, Jin Q, Huang L. 2017. A promising approach to enhance microalgae productivity by exogenous supply of vitamins. Microb. Cell Fact. 16: 219. https://doi.org/10.1186/s12934-017-0834-2
- Wirth R, Pap B, Bojti T, Shetty P, Lakatos G, Bagi Z, et al. 2020. Chlorella vulgaris and its phycosphere in wastewater: Microalgae-bacteria interactions during nutrient removal. Front. Bioeng. Biotechnol. 8: 557572. https://doi.org/10.3389/fbioe.2020.557572
- Liu J, Wu Y, Wu C, Muylaert K, Vyverman W, Yu HQ, et al. 2017. Advanced nutrient removal from surface water by a consortium of attached microalgae and bacteria: A review. Bioresour. Technol. 241: 1127-1137. https://doi.org/10.1016/j.biortech.2017.06.054
- Soltis DE, Soltis PS. 2003. Applying the bootstrap in phylogeny reconstruction. Stat. Sci. 18: 256-267. https://doi.org/10.1214/ss/1063994980
- Kim JH, Affan A, Jang J, Kang MH, Ko AR, Jeon SM, et al. 2015. Morphological, molecular, and biochemical characterization of astaxanthin-producing green microalga Haematococcus sp. KORDI03 (Haematococcaceae, Chlorophyta) isolated from Korea. J. Microbiol. Biotechnol. 25: 238-246. https://doi.org/10.4014/jmb.1410.10032
- Jeon SM, Kim JH, Kim T, Park A, Ko AR, Ju SJ, et al. 2015. Morphological, molecular, and biochemical characterization of monounsaturated fatty acids-rich Chlamydomonas sp. KIOST-1 isolated from Korea. J. Microbiol. Biotechnol. 25: 723-731. https://doi.org/10.4014/jmb.1412.12056
- Rippka R, Stanier RY, Deruelles J, Herdman M, Waterbury JB. 1979. Generic assignments, strain histories and properties of pure cultures of cyanobacteria. Microbiology 111: 1-61. https://doi.org/10.1099/00221287-111-1-1
- Reasoner DJ, Geldreich EE. 1985. A new medium for the enumeration and subculture of bacteria from potable water. Appl. Environ. Microbiol. 49: 1-7. https://doi.org/10.1128/AEM.49.1.1-7.1985
- Bold HC. 1949. The morphology of Chlamydomonas chlamydogama, sp. Nov. Bull. Torrey Bot. Club. 76: 101-108. https://doi.org/10.2307/2482218
- Fabregas J, Dominguez A, Regueiro M, Maseda A, Otero A. 2000. Optimization of culture medium for the continuous cultivation of the microalga Haematococcus pluvialis. Appl. Microbiol. Biotechnol. 53: 530-535. https://doi.org/10.1007/s002530051652
- Laurens LM, Dempster TA, Jones HD, Wolfrum EJ, Van Wychen S, McAllister JS, et al. 2012. Algal biomass constituent analysis: method uncertainties and investigation of the underlying measuring chemistries. Anal. Chem. 84: 1879-1887. https://doi.org/10.1021/ac202668c
- Van Wychen S, Laurens LML. 2016. Determination of total carbohydrates in algal biomass: Laboratory analytical procedure (LAP). NREL, Golden, CO, United States.
- Mishra SK, Suh WI, Farooq W, Moon M, Shrivastav A, Park MS, et al. 2014. Rapid quantification of microalgal lipids in aqueous medium by a simple colorimetric method. Bioresour. Technol. 155: 330-333. https://doi.org/10.1016/j.biortech.2013.12.077
- Breuer G, Evers WAC, de Vree JH, Kleinegris DMM, Martens DE, Wijffels RH, et al. 2013. Analysis of fatty acid content and composition in microalgae. J. Vis. Exp. 80: 50628.
- Du Z, Hu B, Ma X, Cheng Y, Liu Y, Lin X, et al. 2013. Catalytic pyrolysis of microalgae and their three major components: carbohydrates, proteins, and lipids. Bioresour. Technol. 130: 777-782. https://doi.org/10.1016/j.biortech.2012.12.115
- Given PH, Weldon D, Zoeller JH. 1986. Calculation of calorific values of coals from ultimate analyses: theoretical basis and geochemical implications. Fuel 65: 849-854. https://doi.org/10.1016/0016-2361(86)90080-3
- Osundeko O, Davies H, Pittman JK. 2013. Oxidative stress-tolerant microalgae strains are highly efficient for biofuel feedstock production on wastewater. Biomass Bioenergy 56: 284-294. https://doi.org/10.1016/j.biombioe.2013.05.027
- Stenclova L, Fucikova K, Kastovsky J, Pazoutova M. 2017. Molecular and morphological delimitation and generic classification of the family Oocystaceae (Trebouxiophyceae, Chlorophyta). J. Phycol. 53: 1263-1282. https://doi.org/10.1111/jpy.12581
- Asker D, Beppu T, Ueda K. 2007. Sphingomonas astaxanthinifaciens sp. nov., a novel astaxanthin-producing bacterium of the family Sphingomonadaceae isolated from Misasa, Tottori, Japan. FEMS Microbiol. Lett. 273: 140-148. https://doi.org/10.1111/j.1574-6968.2007.00760.x
- Krzeminska I, Pawlik-Skowronska B, Trzcinska M, Tys J. 2014. Influence of photoperiods on the growth rate and biomass productivity of green microalgae. Bioprocess Biosyst. Eng. 37: 735-741. https://doi.org/10.1007/s00449-013-1044-x
- Gouveia JD, Ruiz J, van den Broek LAM, Hesselink T, Peters S, Kleinegris DMM, et al. 2017. Botryococcus braunii strains compared for biomass productivity, hydrocarbon and carbohydrate content. J. Biotechnol. 248: 77-86. https://doi.org/10.1016/j.jbiotec.2017.03.008
- Korponai K, Szabo A, Somogyi B, Boros E, Borsodi AK, Jurecska L, et al. 2019. Dual bloom of green algae and purple bacteria in an extremely shallow soda pan. Extremophiles 23: 467-477. https://doi.org/10.1007/s00792-019-01098-4
- Lian J, Wijffels RH, Smidt H, Sipkema D. 2018. The effect of the algal microbiome on industrial production of microalgae. Microb. Biotechnol. 11: 806-818. https://doi.org/10.1111/1751-7915.13296
- Ramanan R, Kim BH, Cho DH, Oh HM, Kim HS. 2016. Algae-bacteria interactions: Evolution, ecology and emerging applications. Biotechnol. Adv. 34: 14-29. https://doi.org/10.1016/j.biotechadv.2015.12.003
- Cho K, Heo J, Cho DH, Tran QG, Yun JH, Lee SM, et al. 2019. Enhancing algal biomass and lipid production by phycospheric bacterial volatiles and possible growth enhancing factor. Algal Res. 37: 186-194. https://doi.org/10.1016/j.algal.2018.11.011
- Perera IA, Abinandan S, Subashchandrabose SR, Venkateswarlu K, Naidu R, Megharaj M. 2019. Advances in the technologies for studying consortia of bacteria and cyanobacteria/microalgae in wastewaters. Crit. Rev. Biotechnol. 39: 709-731. https://doi.org/10.1080/07388551.2019.1597828
- Cho DH, Ramanan R, Heo J, Kang Z, Kim BH, Ahn CY, et al. 2015. Organic carbon, influent microbial diversity and temperature strongly influence algal diversity and biomass in raceway ponds treating raw municipal wastewater. Bioresour. Technol. 191: 481-487. https://doi.org/10.1016/j.biortech.2015.02.013
- Yang S, Wan H, Wang R, Hao D. 2019. Sulfated polysaccharides from Phaeodactylum tricornutum: isolation, structural characteristics, and inhibiting HepG2 growth activity in vitro. Peer J 7: e6409. https://doi.org/10.7717/peerj.6409
- Trabelsi L, Chaieb O, Mnari A, Abid-Essafi S, Aleya L. 2016. Partial characterization and antioxidant and antiproliferative activities of the aqueous extracellular polysaccharides from the thermophilic microalgae Graesiella sp. BMC Complement. Altern. Med. 16: 210. https://doi.org/10.1186/s12906-016-1198-6
- Lopez G, Yate C, Ramos FA, Cala MP, Restrepo S, Baena S. 2019. Production of polyunsaturated fatty acids and lipids from autotrophic, mixotrophic and heterotrophic cultivation of Galdieria sp. strain USBA-GBX-832. Sci. Rep. 9: 10791. https://doi.org/10.1038/s41598-019-46645-3
- Kothri M, Mavrommati M, Elazzazy AM, Baeshen MN, Moussa TAA, Aggelis G. 2020. Microbial sources of polyunsaturated fatty acids (PUFAs) and the prospect of organic residues and wastes as growth media for PUFA-producing microorganisms. FEMS Microbiol. Lett. 367: fnaa028. https://doi.org/10.1093/femsle/fnaa028
- Tocher DR, Betancor MB, Sprague M, Olsen RE, Napier JA. 2019. Omega-3 long-chain polyunsaturated fatty acids, EPA and DHA: Bridging the gap between supply and demand. Nutrients 11: 89. https://doi.org/10.3390/nu11010089
- Chauton MS, Reitan KI, Norsker NH, Tveteras R, Kleivdal HT. 2015. A techno-economic analysis of industrial production of marine microalgae as a source of EPA and DHA-rich raw material for aquafeed: research challenges and possibilities. Aquaculture 436: 95-103. https://doi.org/10.1016/j.aquaculture.2014.10.038
- Arguelles EDLR, Laurena AC, Monsalud RG, Martinez-Goss MR. 2017. Fatty acid profile and fuel-derived physico-chemical properties of biodiesel obtained from an indigenous green microalga, Desmodesmus sp. (I-AU1), as potential source of renewable lipid and high quality biodiesel. J. Appl. Phycol. 30: 411-419. https://doi.org/10.1007/s10811-017-1264-6