Biotechnological impacts of Halomonas: a promising cell factory for industrially relevant biomolecules

References

• Abdelkafi, S., Sayadi, S., Ali Gam, Z. B., Casalot, L., & Labat, M. (2006). Bioconversion of ferulic acid to vanillic acid by Halomonas elongata isolated from table-olive fermentation. FEMS Microbiology Letters, 262(1), 115–120. https://doi.org/10.1111/j.1574-6968.2006.00381.x
   PubMed Web of Science ®Google Scholar
• Abdrabo, A. A. M., Ibrahim, A. H. H., Hassan, S. W., & Abdul-Raouf, M. U. (2018). Antimicrobial and anti-tumor activities of exopolysaccharides produced by the biofilm of marine Halomonas saccharevitans AB2 isolated from Suez Gulf, Egypt. Egyptian Journal of Aquatic Biology and Fisheries, 22(5), 99–119. https://doi.org/10.21608/EJABF.2018.22007
   Google Scholar
• Amjres, H., Bejar, V., Quesada, E., Carranza, D., Abrini, J., Sinquin, C., Ratiskol, J., Colliec-Jouault, S., & Llamas, I. (2015). Characterization of haloglycan, an exopolysaccharide produced by Halomonas stenophila HK30. International Journal of Biological Macromolecules, 72, 117–124. https://doi.org/10.1016/j.ijbiomac.2014.07.052
   PubMed Web of Science ®Google Scholar
• Amoozegar, M. A., Ghazanfari, N., & Didari, M. (2012). Lead and cadmium bioremoval by Halomonas sp., an exopolysaccharide-producing halophilic bacterium. Progress in Biological Sciences, 2(1), 1–11. https://doi.org/10.22059/PBS.2012.24820
   Google Scholar
• Arahal, D. R., & Ventosa, A. (2006). The family Halomonadaceae. In M. Dworkin, S. Falkow, E. Rosenberg, K.-H. Schleifer, & E. Stackebrandt (Eds.), The prokaryotes (3rd ed., Vol. 6, pp. 811–835), Proteobacteria: gamma subclass. Springer.
   Google Scholar
• Arahal, D. R., Vreeland, R. H., Litchfield, C. D., Mormile, M. R., Tindall, B. J., Oren, A., Bejar, V., Quesada, E., & Ventosa, A. (2007). Recommended minimal standards for describing new taxa of the family Halomonadaceae. International Journal of Systematic and Evolutionary Microbiology, 57(10), 2436–2446. https://doi.org/10.1099/ijs.0.65430-0
   PubMed Web of Science ®Google Scholar
• Arai, S., Yonezawa, Y., Ishibashi, M., Matsumoto, F., Adachi, M., Tamada, T., Tokunaga, H., Blaber, M., Tokunag, M., & Kuroki, R. (2014). Structural characteristics of alkaline phosphatase from the moderately halophilic bacterium Halomonas sp. 593. Acta Crystallographica: Section D, Biological Crystallography, 70(3), 811–820. https://doi.org/10.1107/S1399004713033609
   PubMedGoogle Scholar
• Arco, Y., Llamas, I., Martínez-Checa, F., Argandona, M., Quesada, E., & Del Moral, A. (2005). epsABCJ genes are involved in the biosynthesis of the exopolysaccharide mauran produced by Halomonas maura. Microbiology (Reading, England), 151(9), 2841–2851. https://doi.org/10.1099/mic.0.27981-0
   PubMed Web of Science ®Google Scholar
• Arias, S., Del Moral, A., Ferrer, M. R., Tallon, R., Quesada, E., & Bejar, V. (2003). Mauran, an exopolysaccharide produced by the halophilic bacterium Halomonas maura, with a novel composition and interesting properties for biotechnology. Extremophiles, 7(4), 319–326. https://doi.org/10.1007/s00792-003-0325-8
   PubMed Web of Science ®Google Scholar
• Asksonthong, R., Siripongvutikorn, S., & Usawakesmanee, W. (2018). Heavy metal removal ability of Halomonas elongata and Tetragenococcus halophilus in a media model system as affected by pH and incubation time. International Food Research Journal, 25(1), 234–240.
   Web of Science ®Google Scholar
• Aston, J. E., & Peyton, B. M. (2007). Response of Halomonas campisalis to saline stress: Changes in growth kinetics, compatible solute production and membrane phospholipid fatty acid composition. FEMS Microbiology Letters, 274(2), 196–203. https://doi.org/10.1111/j.1574-6968.2007.00851.x
   PubMed Web of Science ®Google Scholar
• Biswas, J., Bose, P., Mandal, S., & Paul, A. K. (2018). Reduction of hexavalent chromium by a moderately halophilic bacterium, Halomonas smyrnensis KS802 under saline environment. Environmental Sustainability, 1(4), 411–423. https://doi.org/10.1007/s42398-018-00037-x
   Google Scholar
• Biswas, J., Ganguly, J., & Paul, A. K. (2015). Partial characterization of an extracellular polysaccharide produced by a moderately halophilic bacterium Halomonas xianhensis SUR308. Biofouling, 31(9–10), 735–744. https://doi.org/10.1080/08927014.2015.1106479
   PubMed Web of Science ®Google Scholar
• Biswas, J., Mandal, S., & Paul, A. K. (2015). Production, partial purification and some bio-physicochemical properties of EPS produced by Halomonas xianhensis SUR308 isolated from a saltern environment. Journal of Biologically Active Products from Nature, 5(2), 108–119. https://doi.org/10.1080/22311866.2015.1038852
   Google Scholar
• Biswas, J., & Paul, A. K. (2017). Diversity and production of extracellular polysaccharide by halophilic microorganisms. Biodiversity International Journal, 1(2), 32–39. https://doi.org/10.15406/bij.2017.01.00006
   Google Scholar
• Bouchotroch, S., Quesada, E., Del Moral, A., Llamas, I., & Bejar, V. (2001). Halomonas maura sp. nov., a novel moderately halophilic, exopolysaccharide-producing bacterium. International Journal of Systematic and Evolutionary Microbiology, 51(5), 1625–1632. https://doi.org/10.1099/00207713-51-5-1625
   PubMed Web of Science ®Google Scholar
• Cai, L., Tan, D., Aibaidula, G., Dong, X. R., Chen, J. C., Tian, W. D., & Chen, G. Q. (2011). Comparative genomics study of polyhydroxyalkanoates (PHA) and ectoine relevant genes from Halomonas sp. TD01 revealed extensive horizontal gene transfer events and co-evolutionary relationships. Microbial Cell Factories, 10(1), 1–15. https://doi.org/10.1186/1475-2859-10-88
   PubMed Web of Science ®Google Scholar
• Calvo, C., Martinez-Checa, F., Toledo, F. L., Porcel, J., & Quesada, E. (2002). Characteristics of bioemulsifiers synthesized in crude oil media by Halomonas eurihalina and their effectiveness in the isolation of bacteria able to grow in the presence of hydrocarbons. Applied Microbiology and Biotechnology, 60(3), 347–351. https://doi.org/10.1007/s00253-002-1115-4
   PubMed Web of Science ®Google Scholar
• Cánovas, D., Vargas, C., Kneip, S., Moron, M. J., Ventosa, A., Bremer, E., & Nieto, J. J. (2000). Genes for the synthesis of the osmoprotectant glycine betaine from choline in the moderately halophilic bacterium Halomonas elongata DSM 3043the EMBL accession number for the sequence reported in this paper is AJ238780. Microbiology (Reading, England), 146(2), 455–463. https://doi.org/10.1099/00221287-146-2-455
   PubMed Web of Science ®Google Scholar
• Carlson, R. P., Oshota, O., Shipman, M., Caserta, J. A., Hu, P., Saunders, C. W., Xu, J., Jay, Z. J., Reeder, N., Richards, A., Pettigrew, C., & Peyton, B. M. (2016). Integrated molecular, physiological and in silico characterization of two Halomonas isolates from industrial brine. Extremophiles, 20(3), 261–274. https://doi.org/10.1007/s00792-015-0806-6
   PubMed Web of Science ®Google Scholar
• Chandra, P., & Singh, D. P. (2014). Removal of Cr (VI) by a halotolerant bacterium Halomonas sp. CSB 5 isolated from Sambhar salt lake Rajasthan (India). Cellular and Molecular Biology, 60(5), 64–72.
   PubMed Web of Science ®Google Scholar
• Cheffi, M., Hentati, D., Chebbi, A., Mhiri, N., Sayadi, S., Marques, A. M., & Chamkha, M. (2020). Isolation and characterization of a newly naphthalene-degrading Halomonas pacifica, strain Cnaph3: Biodegradation and biosurfactant production studies. 3 Biotech, 10(3), 1–15. https://doi.org/10.1007/s13205-020-2085-x
   PubMedGoogle Scholar
• Chen, G. Q., & Jiang, X. (2018). Next generation industrial biotechnology based on extremophilic bacteria. Current Opinion in Biotechnology, 50, 94–100. https://doi.org/10.1016/j.copbio.2017.11.016
   PubMed Web of Science ®Google Scholar
• Chikkanna, A., Ghosh, D., & Kishore, A. (2018). Expression and characterization of a potential exopolysaccharide from a newly isolated halophilic thermotolerant bacteria Halomonas nitroreducens strain WB1. PeerJ, 6, 4684. https://doi.org/10.7717/peerj.4684
   PubMed Web of Science ®Google Scholar
• Coronado, M. J., Vargas, C., Hofemeister, J., Ventosa, A., & Nieto, J. J. (2000). Production and biochemical characterization of an α-amylase from the moderate halophile Halomonas meridiana. FEMS Microbiology Letters, 183(1), 67–71. https://doi.org/10.1111/j.1574-6968.2000.tb08935.x
   PubMed Web of Science ®Google Scholar
• Cristea, A., Baricz, A., Leopold, N., Floare, C. G., Borodi, G., Kacso, I., Tripon, S., Bulzu, P. A., Andrei, A.-S., Cadar, O., Levei, E. A., & Banciu, H. L. (2018). Polyhydroxybutyrate production by an extremely halotolerant Halomonas elongata strain isolated from the hypersaline meromictic Fara Fund Lake (Transylvanian Basin, Romania). Journal of Applied Microbiology, 125(5), 1343–1357. https://doi.org/10.1111/jam.14029
   PubMed Web of Science ®Google Scholar
• Cummings, S. P., & Gilmour, D. J. (1995). The effect of NaCl on the growth of a Halomonas species: Accumulation and utilization of compatible solutes. Microbiology (Reading, England), 141(6), 1413–1418. https://doi.org/10.1099/13500872-141-6-1413
   PubMed Web of Science ®Google Scholar
• de la Haba, R. R., Arahal, D. R., Marquez, M. C., & Ventosa, A. (2010). Phylogenetic relationships within the family Halomonadaceae based on comparative 23S and 16S rRNA gene sequence analysis. International Journal of Systematic and Evolutionary Microbiology, 60(4), 737–748. https://doi.org/10.1099/ijs.0.013979-0
   PubMed Web of Science ®Google Scholar
• de la Haba, R. R., Marquez, M. C., Papke, R. T., & Ventosa, A. (2012). Multilocus sequence analysis of the family Halomonadaceae. International Journal of Systematic and Evolutionary Microbiology, 62(3), 520–538. https://doi.org/10.1099/ijs.0.032938-0
   PubMed Web of Science ®Google Scholar
• de la Haba, R. R., Sanchez-Porro, C., & Ventosa, A. (2011). Taxonomy, phylogeny and biotechnological interest of the family Halomonadaceae. In A. Ventosa, A. Oren, & Y. Ma (Eds.), Halophiles and hypersaline environments (pp. 27–64). Springer. https://doi.org/10.1007/978-3-642-20198-1_3
   Google Scholar
• de Souza, P. M. (2010). Application of microbial α-amylase in industry-A review. Brazilian Journal of Microbiology, 41(4), 850–861. https://doi.org/10.1590/S1517-83822010000400004
   PubMed Web of Science ®Google Scholar
• de Souza, M. P., Amini, A., Dojka, M. A., Pickering, I. J., Dawson, S. C., Pace, N. R., & Terry, N. (2001). Identification and characterization of bacteria in a selenium-contaminated hypersaline evaporation pond. Applied and Environmental Microbiology, 67(9), 3785–3794. https://doi.org/10.1128/AEM.67.9.3785-3794.2001
   PubMed Web of Science ®Google Scholar
• Dhasayan, A., Kiran, G. S., & Selvin, J. (2014). Production and Characterization of Glycolipid Biosurfactant by Halomonas sp. MB-30 for Potential Application in Enhanced oil Recovery. Applied Biochemistry and Biotechnology, 174(7), 2571–2584. https://doi.org/10.1007/s12010-014-1209-3
   PubMed Web of Science ®Google Scholar
• Diaz-Cardenas, C., Cantillo, A., Rojas, L. Y., Sandoval, T., Fiorentino, S., Robles, J., Ramos, F. A., Zambrano, M. M., & Baena, S. (2017). Microbial diversity of saline environments: Searching for cytotoxic activities. AMB Express, 7(1), 1–16. https://doi.org/10.1186/s13568-017-0527-6
   PubMed Web of Science ®Google Scholar
• Diken, E., Ozer, T., Arikan, M., Emrence, Z., Oner, E. T., Ustek, D., & Arga, K. Y. (2015). Genomic analysis reveals the biotechnological and industrial potential of levan producing halophilic extremophile, Halomonas smyrnensis AAD6T. SpringerPlus, 4(1), 1–11. https://doi.org/10.1186/s40064-015-1184-3
   PubMedGoogle Scholar
• Dobson, S. J., McMeekin, T. A., & Franzmann, P. D. (1993). Phylogenetic relationships between some members of the genera Deleya, Halomonas, and Halovibrio. International Journal of Systematic and Evolutionary Microbiology, 43(4), 665–673. https://doi.org/10.1099/00207713-43-4-665
   Web of Science ®Google Scholar
• Donio, M. B. S., Ronica, F. A., Viji, V. T., Velmurugan, S., Jenifer, J. S. C. A., Michaelbabu, M., Dhar, P., & Citarasu, T. (2013). Halomonas sp. BS4, a biosurfactant producing halophilic bacterium isolated from solar salt works in India and their biomedical importance. Springerplus, 2(1), 149. https://doi.org/10.1186/2193-1801-2-149
   PubMedGoogle Scholar
• Dubey, S., & Mishra, S. (2021). Efficient production of polyhydroxyalkanoate through halophilic bacteria utilizing algal biodiesel waste residue. Frontiers in Bioengineering and Biotechnology, 9, 85. https://doi.org/10.3389/fbioe.2021.624859
   Web of Science ®Google Scholar
• Edbeib, M. F., Wahab, R. A., & Huyop, F. (2016). Halophiles: Biology, adaptation, and their role in decontamination of hypersaline environments. World Journal of Microbiology & Biotechnology, 32(8), 1–23. https://doi.org/10.1007/s11274-016-2081-9
   PubMed Web of Science ®Google Scholar
• Eslami, M., Amoozegar, M. A., & Asad, S. (2016). Isolation, cloning and characterization of an azoreductase from the halophilic bacterium Halomonas elongata. International Journal of Biological Macromolecules, 85, 111–116. https://doi.org/10.1016/j.ijbiomac.2015.12.065
   PubMed Web of Science ®Google Scholar
• Fatollahi, P., Ghasemi, M., Yazdian, F., & Sadeghi, A. (2021). Ectoine production in bioreactor by Halomonas elongata DSM2581: Using MWCNT and Fe-nanoparticle. Biotechnology Progress, 37(1), e3073. https://doi.org/10.1002/btpr.3073
   PubMed Web of Science ®Google Scholar
• Fernandez, A. B., Vera-Gargallo, B., Sanchez-Porro, C., Ghai, R., Papke, R. T., Rodriguez-Valera, F., & Ventosa, A. (2014). Comparison of prokaryotic community structure from Mediterranean and Atlantic saltern concentrator ponds by a metagenomic approach. Frontiers in Microbiology, 5, 196. https://doi.org/10.3389/fmicb.2014.00196
   PubMed Web of Science ®Google Scholar
• Focardi, S., Pepi, M., Landi, G., Gasperini, S., Ruta, M., DiBiasio, P., & Focardi, S. E. (2012). Hexavalent chromium reduction by whole cells and cell free extract of the moderate halophilic bacterial strain Halomonas sp. TA-04. International Biodeterioration & Biodegradation, 66(1), 63–70. https://doi.org/10.1016/j.ibiod.2011.11.003
   Web of Science ®Google Scholar
• Francis, A. J., Dodge, C. J., Gillow, J. B., & Papenguth, H. W. (2000). Biotransformation of uranium compounds in high ionic strength brine by a halophilic bacterium under denitrifying conditions. Environmental Science & Technology, 34(11), 2311–2317. https://doi.org/10.1021/es991251e
   Web of Science ®Google Scholar
• Gadda, G., & McAllister-Wilkins, E. E. (2003). Cloning, expression, and purification of choline dehydrogenase from the moderate halophile Halomonas elongata. Applied and Environmental Microbiology, 69(4), 2126–2132. https://doi.org/10.1128/AEM.69.4.2126-2132.2003
   PubMed Web of Science ®Google Scholar
• Gao, M., Du, D., Bo, Z., & Sui, L. (2019). Poly-β-hydroxybutyrate (PHB)-accumulating Halomonas improves the survival, growth, robustness and modifies the gut microbial composition of Litopenaeus vannameipost larvae. Aquaculture, 500, 607–612. https://doi.org/10.1016/j.aquaculture.2018.10.032
   Web of Science ®Google Scholar
• Garrity, G. M., Bell, J. A., & Lilburn, T. G. (2003). Taxonomic outline of the Procaryotes. In D. R. Boone & R. W. Castenholz (Eds.), Bergey’s manual of systematic bacteriology (2nd ed.). New York: Springer-Verlag. doi:10.1007/bergeysoutline200405.
   Google Scholar
• Ghate, S. D., Arun, A. B., Rao, S. S., Kumar, S. T., Kandiyil, M. K., Saptami, K., & Rekha, P. D. (2021). Genome analysis of a halophilic bacterium Halomonas malpeensis YU-PRIM-29T reveals its exopolysaccharide and pigment producing capabilities. Scientific Reports, 11(1), 1–14. https://doi.org/10.1038/s41598-021-81395-1
   PubMed Web of Science ®Google Scholar
• Grammann, K., Volke, A., & Kunte, H. J. (2002). New type of osmoregulated solute transporter identified in halophilic members of the bacteria domain: TRAP transporter TeaABC mediates uptake of ectoine and hydroxyectoine in Halomonas elongata DSM 2581T. Journal of Bacteriology, 184(11), 3078–3085. https://doi.org/10.1128/JB.184.11.3078-3085.2002
   PubMed Web of Science ®Google Scholar
• Gunaratnam, M., & Grant, M. H. (2008). Cr(vi) inhibits DNA, RNA and protein syntheses in hepatocytes: Involvement of glutathione reductase, reduced glutathione and DT-diaphorase. Toxicology in Vitro, 22(4), 879–886. https://doi.org/10.1016/j.tiv.2008.01.005
   PubMed Web of Science ®Google Scholar
• Guo, G., Hao, J., Tian, F., Liu, C., Ding, K., Xu, J., Zhou, W., & Guan, Z. (2020). Decolorization and detoxification of azo dye by halo-alkaliphilic bacterial consortium: Systematic investigations of performance, pathway and metagenome. Ecotoxicology and Environmental Safety, 204, 111073. https://doi.org/10.1016/j.ecoenv.2020.111073
   PubMed Web of Science ®Google Scholar
• Guo, J., Zhou, J., Wang, D., Tian, C., Wang, P., & Uddin, M. S. (2008). A novel moderately halophilic bacterium for decolorizing azo dye under high salt condition. Biodegradation, 19(1), 15–19. https://doi.org/10.1007/s10532-007-9110-1
   PubMed Web of Science ®Google Scholar
• Gutierrez-Arnillas, E., Arellano, M., Deive, F. J., Rodriguez, A., & Sanroman, M. A. (2017). Unravelling the suitability of biological induction for halophilic lipase production by Halomonas sp. LM1C cultures. Bioresource Technology, 239, 368–377. https://doi.org/10.1016/j.biortech.2017.04.128
   PubMed Web of Science ®Google Scholar
• Gutierrez, T., Biller, D. V., Shimmield, T., & Green, D. H. (2012). Metal binding properties of the EPS produced by Halomonas sp. TG39 and its potential in enhancing trace element bioavailability to eukaryotic phytoplankton. Biometals, 25(6), 1185–1194. https://doi.org/10.1007/s10534-012-9581-3
   PubMed Web of Science ®Google Scholar
• Gutierrez, T., Mulloy, B., Black, K., & Green, D. H. (2007). Glycoprotein emulsifiers from two marine Halomonas species: Chemical and physical characterization. Journal of Applied Microbiology, 103(5), 1716–1727. https://doi.org/10.1111/j.1365-2672.2007.03407.x
   PubMed Web of Science ®Google Scholar
• Guzman, H., Van Thuoc, D., Martín, J., Hatti-Kaul, R., & Quillaguaman, J. (2009). A process for the production of ectoine and poly (3-hydroxybutyrate) by Halomonas boliviensis. Applied Microbiology and Biotechnology, 84(6), 1069–1077. https://doi.org/10.1007/s00253-009-2036-2
   PubMed Web of Science ®Google Scholar
• Hajizadeh, N., Heris, Y. S., Vahed, S. Z., Vallipour, J., Hejazi, M. A., Golabi, S. M., Zeynali, A., & Hejazi, M. S. (2015). Biodegradation of para amino acetanilide by Halomonas sp. TBZ3. Jundishapur Journal of Microbiology, 8(9). https://doi.org/10.5812/jjm.18622
   PubMed Web of Science ®Google Scholar
• He, J., Zhen, Q., Qiu, N., Liu, Z., Wang, B., Shao, Z., & Yu, Z. (2009). Medium optimization for the production of a novel bioflocculant from Halomonas sp. V3a’ using response surface methodology. Bioresource Technology, 100(23), 5922–5927. https://doi.org/10.1016/j.biortech.2009.06.087
   PubMed Web of Science ®Google Scholar
• Homann, V. V., Sandy, M., Tincu, J. A., Templeton, A. S., Tebo, B. M., & Butler, A. (2009). Loihichelins A− F, a suite of amphiphilic siderophores produced by the marine bacterium Halomonas LOB-5. Journal of Natural Products, 72(5), 884–888. https://doi.org/10.1021/np800640h
   PubMed Web of Science ®Google Scholar
• Jain, R., Jha, S., Mahatma, M. K., Jha, A., & Kumar, G. N. (2016). Characterization of arsenite tolerant Halomonas sp. Alang-4, originated from heavy metal polluted shore of Gulf of Cambay. Journal of Environmental Science and Health, Part A, 51(6), 478–486. https://doi.org/10.1080/10934529.2015.1128717
   PubMed Web of Science ®Google Scholar
• Jiang, X. R., Yao, Z. H., & Chen, G. Q. (2017). Controlling cell volume for efficient PHB production by Halomonas. Metabolic Engineering, 44, 30–37. https://doi.org/10.1016/j.ymben.2017.09.004
   PubMed Web of Science ®Google Scholar
• Kahrarian, Z., Taran, M., Alimoradi, M., & Tajehmiri, A. (2019). Biological removal of cadmium by Halomonas elongata IBRC-M10433 in different conditions: Optimization by Taguchi statistical approach. Asian Journal of Research in Biosciences, 1(1), 7–13.
   Google Scholar
• Kanapathipillai, M., Lentzen, G., Sierks, M., & Park, C. B. (2005). Ectoine and hydroxyectoine inhibit aggregation and neurotoxicity of Alzheimer’s β-amyloid. FEBS Letters, 579(21), 4775–4780. https://doi.org/10.1016/j.febslet.2005.07.057
   PubMed Web of Science ®Google Scholar
• Kaniuk, Ł., & Stachewicz, U. (2021). Development and advantages of biodegradable PHA polymers based on electrospun PHBV fibers for tissue engineering and other biomedical applications. ACS Biomaterials Science & Engineering, 7(12), 5339–5362. https://doi.org/10.1021/acsbiomaterials.1c00757
   PubMed Web of Science ®Google Scholar
• Kawata, Y., & Aiba, S. I. (2010). Poly (3-hydroxybutyrate) production by isolated Halomonas sp. KM-1 using waste glycerol. Bioscience, Biotechnology, and Biochemistry, 0912011758. https://doi.org/10.1016/j.jbiosc.2011.11.018
   Web of Science ®Google Scholar
• Kayanadath, S., Nathan, V. K., & Ammini, P. (2019). Anti-biofilm activity of biosurfactant derived from Halomonas sp., a lipolytic marine bacterium from the Bay of Bengal. Microbiology (Reading, England), 88(5), 585–599. https://doi.org/10.1134/S0026261719050072
   Web of Science ®Google Scholar
• Khmaissa, M., Hadrich, B., Chamkha, M., Sayari, A., & Fendri, A. (2021). Production of a halotolerant lipase from Halomonas sp. strain C2SS100: Optimization by response-surface methodology and application in detergent formulations. Journal of Surfactants and Detergents. https://doi.org/10.1002/jsde.12563
   Web of Science ®Google Scholar
• Kim, K. K., Lee, K. C., Oh, H. M., & Lee, J. S. (2010). Halomonas stevensii sp. nov., Halomonas hamiltonii sp. nov. and Halomonas johnsoniae sp. nov., isolated from a renal care centre. International Journal of Systematic and Evolutionary Microbiology, 60(2), 369–377. https://doi.org/10.1099/ijs.0.004424-0
   PubMed Web of Science ®Google Scholar
• Kleinsteuber, S., Müller, R. H., & Babel, W. (2001). Expression of the 2, 4-D degradative pathway of pJP4 in an alkaliphilic, moderately halophilic soda lake isolates, Halomonas sp. EF43. Extremophiles, 5(6), 375–384. https://doi.org/10.1007/s007920100202
   PubMed Web of Science ®Google Scholar
• Kshirsagar, P. R., Suttar, R., Nilegaonkar, S. S., Pradhan, S., & Kanekar, P. P. (2013). Scale up production of polyhydroxyalkanoate (PHA) at different aeration, agitation and controlled dissolved oxygen levels in fermenter using Halomonas campisalis MCM B-1027. Journal of Biochemical Technology, 4(1), 512–517.
   Google Scholar
• Kucera, D., Pernicova, I., Kovalcik, A., Koller, M., Mullerova, L., Sedlacek, P., Mravec, F., Nebesarova, J., Kalina, M., Marova, I., Krzyzanek, V., & Obruca, S. (2018). Characterization of the promising poly (3-hydroxybutyrate) producing halophilic bacterium Halomonas halophila. Bioresource Technology, 256, 552–556. https://doi.org/10.1016/j.biortech.2018.02.062
   PubMed Web of Science ®Google Scholar
• Kulkarni, S. O., Kanekar, P. P., Jog, J. P., Sarnaik, S. S., & Nilegaonkar, S. S. (2015). Production of copolymer, poly (hydroxybutyrate-co-hydroxyvalerate) by Halomonas campisalis MCM B-1027 using agro-wastes. International Journal of Biological Macromolecules, 72, 784–789. https://doi.org/10.1016/j.biortech.2011.03.054
   PubMed Web of Science ®Google Scholar
• Kumar, S., Karan, R., Kapoor, S., Singh, S. P., & Khare, S. K. (2012). Screening and isolation of halophilic bacteria producing industrially important enzymes. Brazilian Journal of Microbiology, 43(4), 1595–1603. https://doi.org/10.1590/S1517-838220120004000044
   PubMed Web of Science ®Google Scholar
• Kunte, H. J., Lentzen, G., & Galinski, E. (2014). Industrial production of the cell protectant ectoine: Protection mechanisms, processes, and products. Current Biotechnology, 3(1), 10–25. https://doi.org/10.2174/22115501113026660037
   Google Scholar
• Lang, Y. J., Bai, L., Ren, Y. N., Zhang, L. H., & Nagata, S. (2011). Production of ectoine through a combined process that uses both growing and resting cells of Halomonas salina DSM 5928T. Extremophiles, 15(2), 303–310. https://doi.org/10.1007/s00792-011-0360-9
   PubMed Web of Science ®Google Scholar
• Ling, C., Qiao, G. Q., Shuai, B. W., Olavarria, K., Yin, J., Xiang, R. J., Song, K. N., Shen, Y. H., Guo, Y., & Chen, G. Q. (2018). Engineering NADH/NAD+ ratio in Halomonas bluephagenesis for enhanced production of polyhydroxyalkanoates (PHA). Metabolic Engineering, 49, 275–286. https://doi.org/10.1016/j.ymben.2018.09.007
   PubMed Web of Science ®Google Scholar
• Li, T. T., Qu, A., Yuan, X. N., Tan, F. X., Li, X. W., Wang, T., & Zhang, L. H. (2017). Response surface method optimization of ectoine fermentation medium with moderate halophilic bacteria Halomonas sp. H02. In IOP conference series: Earth and environmental science (Vol. 77, No. 1, p. 12019). IOP Publishing.
   Google Scholar
• Liu, J., Li, F., Liu, L., Jiang, P., & Liu, Z. (2013). Inhibitory activity of an extract from a marine bacterium Halomonas sp. HSB07 against the red-tide microalga Gymnodiniumsp.(pyrrophyta). Chinese Journal of Oceanology and Limnology, 31(6), 1241–1247. https://doi.org/10.1007/s00343-013-3160-5
   Web of Science ®Google Scholar
• Liu, M., Liu, H., Shi, M., Jiang, M., Li, L., & Zheng, Y. (2021). Microbial production of ectoine and hydroxyectoine as high-value chemicals. Microbial Cell Factories, 20(1), 1–11. https://doi.org/10.1186/s12934-021-01567-6
   PubMed Web of Science ®Google Scholar
• Llamas, I., Amjres, H., Mata, J. A., Quesada, E., & Bejar, V. (2012). The potential biotechnological applications of the exopolysaccharide produced by the halophilic bacterium Halomonas almeriensis. Molecules, 17(6), 7103–7120. https://doi.org/10.3390/molecules17067103
   PubMed Web of Science ®Google Scholar
• Ma, H., Zhao, Y., Huang, W., Zhang, L., Wu, F., Ye, J., & Chen, G. Q. (2020). Rational flux-tuning of Halomonas bluephagenesis for co-production of bioplastic PHB and ectoine. Nature Communications, 11(1), 1–12. https://doi.org/10.1038/s41467-020-17223-3
   Google Scholar
• Mabrouk, M. E., Arayes, M. A., & Sabry, S. A. (2014). Hexavalent chromium reduction by chromate-resistant haloalkaliphilic Halomonas sp. M-Cr newly isolated from tannery effluent. Biotechnology & Biotechnological Equipment, 28(4), 659–667. https://doi.org/10.1080/13102818.2014.937092
   PubMed Web of Science ®Google Scholar
• Martin, D., Dodds, K., Butler, I. B., & Ngwenya, B. T. (2013). Carbonate precipitation under pressure for bioengineering in the anaerobic subsurface via denitrification. Environmental Science & Technology, 47(15), 8692–8699. https://doi.org/10.1021/es401270q
   PubMed Web of Science ®Google Scholar
• Martinez-Checa, F., Toledo, F., Vilchez, R., Quesada, E., & Calvo, C. (2002). Yield production, chemical composition, and functional properties of emulsifier H28 synthesized by Halomonas eurihalina strain H-28 in media containing various hydrocarbons. Applied Microbiology and Biotechnology, 58(3), 358–363. https://doi.org/10.1007/s00253-001-0903-6
   PubMed Web of Science ®Google Scholar
• Mata, J. A., Martinez-Canovas, J., Quesada, E., & Bejar, V. (2002). A detailed phenotypic characterisation of the type strains of Halomonas species. Systematic and Applied Microbiology, 25(3), 360–375. https://doi.org/10.1078/0723-2020-00122
   PubMed Web of Science ®Google Scholar
• Matsui, T., & Nishino, T. (2016). Transposon‐mediated random gene disruption with moderate halophilic bacteria and its application for halophilic bacterial siderophore analysis. Journal of Basic Microbiology, 56(12), 1354–1359. https://doi.org/10.1002/jobm.201600121
   PubMed Web of Science ®Google Scholar
• Mitra, R., Xu, T., Xiang, H., & Han, J. (2020). Current developments on polyhydroxyalkanoates synthesis by using halophiles as a promising cell factory. Microbial Cell Factories, 19(1), 1–30. https://doi.org/10.1186/s12934-020-01342-z
   PubMed Web of Science ®Google Scholar
• Mnif, S., Chamkha, M., & Sayadi, S. (2009). Isolation and characterization of Halomonas sp. strain C2SS100, a hydrocarbon-degrading bacterium under hypersaline conditions. Journal of Applied Microbiology, 107(3), 785–794. https://doi.org/10.1111/j.1365-2672.2009.04251.x
   PubMed Web of Science ®Google Scholar
• Moharrery, L., Otadi, M., Miraly, N., Rezaei Zangeneh, M. M., & Amiri, R. (2019). Degradation of toluidine red, an oil soluble azo dye by Halomonas strain IP8 at alkaline condition. Chemical Engineering Communications, 206(1), 61–68. https://doi.org/10.1080/00986445.2018.1472587
   Web of Science ®Google Scholar
• Montanez-Barragan, B., Sanz-Martin, J. L., Gutierrez Macias, P., Morato-Cerro, A., Rodriguez-Vazquez, R., & Barragan-Huerta, B. E. (2020). Azo dyes decolorization under high alkalinity and salinity conditions by Halomonas sp. in batch and packed bed reactor. Extremophiles, 24(2), 239–247. https://doi.org/10.1007/s00792-019-01149-w
   PubMed Web of Science ®Google Scholar
• Monzon, C. G., Nisenbaum, M., Herrera Seitz, M. K., & Murialdo, S. E. (2018). New findings on aromatic compounds’ degradation and their metabolic pathways, the biosurfactant production and motility of the halophilic bacterium Halomonas sp. KHS3. Current Microbiology, 75(8), 1108–1118. https://doi.org/10.1007/s00284-018-1497-x
   PubMed Web of Science ®Google Scholar
• Moreno, M. D. L., Sanchez-Porro, C., Piubeli, F., Frias, L., Garcia, M. T., & Mellado, E. (2011). Cloning, characterization and analysis of cat and ben genes from the phenol degrading halophilic bacterium Halomonas organivorans. PloS One, 6(6), e21049. https://doi.org/10.1371/journal.pone.0021049
   PubMed Web of Science ®Google Scholar
• Mukherjee, P., Mitra, A., & Roy, M. (2019). Halomonas rhizobacteria of Avicennia marina of Indian Sundarbans promote rice growth under saline and heavy metal stresses through exopolysaccharide production. Frontiers in Microbiology, 10, 1207. https://doi.org/10.3389/fmicb.2019.01207
   PubMed Web of Science ®Google Scholar
• Murugavelh, S., & Mohanty, K. (2012). Bioreduction of hexavalent chromium by free cells and cell free extracts of Halomonas sp. Chemical Engineering Journal, 203, 415–422. https://doi.org/10.1016/j.cej.2012.07.069
   Web of Science ®Google Scholar
• Murugavelh, S., & Mohanty, K. (2013). Bioreduction of chromate by immobilized cells of Halomonas sp. International Journal of Energy and Environment, 4(2), 349–356.
   Google Scholar
• Murugavelh, S., & Mohanty, K. (2018). Performance of Halomonas sp. to reduce hexavalent chromium in batch and continuous fixed film reactor. Journal of Environmental Chemical Engineering, 6(2), 2561–2567. https://doi.org/10.1016/j.jece.2018.03.037
   Web of Science ®Google Scholar
• Nanca, C. L., Neri, K. D., Ngo, A. C. R., Bennett, R. M., & Dedeles, G. R. (2018). Degradation of polycyclic aromatic hydrocarbons by moderately halophilic bacteria from luzon salt beds. Journal of Health and Pollution, 8(19). https://doi.org/10.5696/2156-9614-8.19.180915
   PubMedGoogle Scholar
• Nikolova, C., & Gutierrez, T. (2021). Biosurfactants and their applications in the oil and gas industry: Current state of knowledge and future perspectives. Frontiers in Bioengineering and Biotechnology, 9, 46. https://doi.org/10.3389/fbioe.2021.626639
   Web of Science ®Google Scholar
• Ojima, T., Saburi, W., Yamamoto, T., & Kudo, T. (2012). Characterization of Halomonas sp. strain H11 α-glucosidase activated by monovalent cations and its application for efficient synthesis of α-D-glucosylglycerol. Applied and Environmental Microbiology, 78(6), 1836–1845. https://doi.org/10.1128/AEM.07514-11
   PubMed Web of Science ®Google Scholar
• Oncescu, T., Oancea, P., Enache, M., Popescu, G., Dumitru, L., & Kamekura, M. (2007). Halophilic bacteria are able to decontaminate dichlorvos, a pesticide, from saline environments. Open Life Sciences, 2(4), 563–573. https://doi.org/10.2478/s11535-007-0037-7
   Web of Science ®Google Scholar
• Oren, A. (2006). The order Haloanaerobiales. In M. Dworkin, S. Falkow, E. Rosenberg, K.-H. Schleifer, & E. Stackebrandt (Eds.), The Prokaryotes. A handbook on the biology of bacteria (Vol. 4, 3rd ed., pp. 804–817). Springer.
   Google Scholar
• Oueriaghli, N., González-Domenech, C. M., Martínez-Checa, F., Muyzer, G., Ventosa, A., Quesada, E., & Béjar, V. (2014). Diversity and distribution of Halomonas in Rambla Salada, a hypersaline environment in the southeast of Spain. FEMS Microbiology Ecology, 87(2), 460–474. https://doi.org/10.1111/1574-6941.12237
   PubMed Web of Science ®Google Scholar
• Ouyang, P., Wang, H., Hajnal, I., Wu, Q., Guo, Y., & Chen, G. Q. (2018). Increasing oxygen availability for improving poly (3-hydroxybutyrate) production by Halomonas. Metabolic Engineering, 45, 20–31. https://doi.org/10.1016/j.ymben.2017.11.006
   PubMed Web of Science ®Google Scholar
• Pastor, J. M., Salvador, M., Argandona, M., Bernal, V., Reina-Bueno, M., Csonka, L. N., Iborra, J. L., Vargas, C., Nieto, J. J., & Canovas, M. (2010). Ectoines in cell stress protection: Uses and biotechnological production. Biotechnology Advances, 28(6), 782–801. https://doi.org/10.1016/j.biotechadv.2010.06.005
   PubMed Web of Science ®Google Scholar
• Pepi, M., Cesaro, A., Liut, G., & Baldi, F. (2005). An Antarctic psychrotrophic bacterium Halomonas sp. ANT-3b, growing on n-hexadecane, produces a new emulsyfying glycolipid. FEMS Microbiology Ecology, 53(1), 157–166. https://doi.org/10.1016/j.femsec.2004.09.013
   PubMed Web of Science ®Google Scholar
• Pinon-Castillo, H. A., Brito, E. M. S., Goni-Urriza, M., Guyoneaud, R., Duran, R., Nevarez-Moorillon, G. V., Gutierrez-Corona, J. F., Caretta, C. A., & Reyna-Lopez, G. E. (2010). Hexavalent chromium reduction by bacterial consortia and pure strains from an alkaline industrial effluent. Journal of Applied Microbiology, 109(6), 2173–2182. https://doi.org/10.1111/j.1365-2672.2010.04849.x
   PubMed Web of Science ®Google Scholar
• Pleissner, D., Lam, W. C., Han, W., Lau, K. Y., Cheung, L. C., Lee, M. W., Lei, H. M., Lo, K. Y., Ng, W. Y., Sun, Z., Melikoglu, M., & Lin, C. S. K. (2014). Fermentative polyhydroxybutyrate production from a novel feedstock derived from bakery waste. BioMed Research International, 2014, 1–8. https://doi.org/10.1155/2014/819474
   Web of Science ®Google Scholar
• Poli, A., Moriello, V. S., Esposito, E., Lama, L., Gambacorta, A., & Nicolaus, B. (2004). Exopolysaccharide production by a new Halomonas strain CRSS isolated from saline lake Cape Russell in Antarctica growing on complex and defined media. Biotechnology Letters, 26(21), 1635–1643. https://doi.org/10.1007/s10529-004-3187-y
   PubMed Web of Science ®Google Scholar
• Pourbabaee, A. A., Bostani, S., Amozzegar, M. A., & Naddaf, R. (2011). Decolorization of cibacron black w-55 under alkaline conditions by new strain of Halomonas sp. isolated from textile effluent. Iranian Journal of Chemistry and Chemical Engineering, 30(4), 63–70. https://doi.org/10.30492/IJCCE.2011.6091
   Google Scholar
• Prabhu, J., Schauwecker, F., Grammel, N., Keller, U., & Bernhard, M. (2004). Functional expression of the ectoine hydroxylase gene (thpD) from Streptomyces chrysomallus in Halomonas elongata. Applied and Environmental Microbiology, 70(5), 3130–3132. https://doi.org/10.1128/AEM.70.5.3130-3132.2004
   PubMed Web of Science ®Google Scholar
• Qin, Q., Ling, C., Zhao, Y., Yang, T., Yin, J., Guo, Y., & Chen, G. Q. (2018). CRISPR/Cas9 editing genome of extremophile Halomonas spp. Metabolic Engineering, 47, 219–229. https://doi.org/10.1016/j.ymben.2018.03.018
   PubMed Web of Science ®Google Scholar
• Quesada, E., Bejar, V., & Calvo, C. (1993). Exopolysaccharide production by Volcaniella eurihalina. Experientia, 49(12), 1037–1041. https://doi.org/10.1007/BF01929910
   Google Scholar
• Ren, Y., Ling, C., Hajnal, I., Wu, Q., & Chen, G. Q. (2018). Construction of Halomonas bluephagenesis capable of high cell density growth for efficient PHA production. Applied Microbiology and Biotechnology, 102(10), 4499–4510. https://doi.org/10.1007/s00253-018-8931-7
   PubMed Web of Science ®Google Scholar
• Riis, V., Kleinsteuber, S., & Babel, W. (2003). Influence of high salinities on the degradation of diesel fuel by bacterial consortia. Canadian Journal of Microbiology, 49(11), 713–721. https://doi.org/10.1139/w03-083
   PubMed Web of Science ®Google Scholar
• Roberts, M. F. (2005). Organic compatible solutes of halotolerant and halophilic microorganisms. Saline Systems, 1(1), 5. https://doi.org/10.1186/1746-1448-1-5
   PubMedGoogle Scholar
• Robinson, T., McMullan, G., Marchant, R., & Nigam, P. (2001). Remediation of dyes in textile effluent: A critical review on current treatment technologies with a proposed alternative. Bioresource Technology, 77(3), 247–255. https://doi.org/10.1016/S0960-8524(00)00080-8
   PubMed Web of Science ®Google Scholar
• Ruiz-Ruiz, C., Srivastava, G. K., Carranza, D., Mata, J. A., Llamas, I., Santamaria, M., Quesada, E., & Molina, I. J. (2011). An exopolysaccharide produced by the novel halophilic bacterium Halomonas stenophila strain B100 selectively induces apoptosis in human T leukaemia cells. Applied Microbiology and Biotechnology, 89(2), 345–355. https://doi.org/10.1007/s00253-010-2886-7
   PubMed Web of Science ®Google Scholar
• Saglam, R. O., Genc, S., & Oner, E. T. (2020). Evaluation of the potential use of Levan polysaccharide in paper conservation. Advances in Polymer Technology, 2020, 1–9. https://doi.org/10.1155/2020/1416491
   Web of Science ®Google Scholar
• Selvi, S. S., Haskoylu, M. E., Genç, S., & Oner, E. T. (2021). Synthesis and characterization of levan hydrogels and their use for resveratrol release. Journal of Bioactive and Compatible Polymers, 36(6), 464–480. https://doi.org/10.1177/08839115211055725
   Web of Science ®Google Scholar
• Severin, J., Wohlfarth, A., & Galinski, E. A. (1992). The predominant role of recently discovered tetrahydropyrimidines for the osmoadaptation of halophilic eubacteria. Microbiology (Reading, England), 138(8), 1629–1638. https://doi.org/10.1099/00221287-138-8-1629
   Web of Science ®Google Scholar
• Seyedi, Z. S., Zahraei, Z., & Jookar Kashi, F. (2020). Decolorization of reactive black 5 and reactive red 152 Azo dyes by new haloalkaliphilic bacteria isolated from the textile wastewater. Current Microbiology, 77(9), 2084–2092. https://doi.org/10.1007/s00284-020-02039-7
   PubMed Web of Science ®Google Scholar
• Shapovalova, A. A., Khijniak, T. V., Tourova, T. P., & Sorokin, D. Y. (2009). Halomonas chromatireducens sp. nov., a new denitrifying facultatively haloalkaliphilic bacterium from solonchak soil capable of aerobic chromate reduction. Microbiology (Reading, England), 78(1), 102–111. https://doi.org/10.1134/S0026261709010135
   Web of Science ®Google Scholar
• Sharma, D., Bhardwaj, K. K., & Gupta, R. (2022). Immobilization and applications of esterases. Biocatalysis and Biotransformation, 40(3), 153–168. https://doi.org/10.1080/10242422.2021.2013825
   Web of Science ®Google Scholar
• Shekhar, S., Sundaramanickam, A., & Balasubramanian, T. (2015). Biosurfactant producing microbes and their potential applications: A review. Critical Reviews in Environmental Science and Technology, 45(14), 1522–1554. https://doi.org/10.1080/10643389.2014.955631
   Web of Science ®Google Scholar
• Shivanand, P., Mugeraya, G., & Kumar, A. (2013). Utilization of renewable agricultural residues for the production of extracellular halostable cellulase from newly isolated Halomonas sp. strain PS47. Annals of Microbiology, 63(4), 1257–1263. https://doi.org/10.1007/s13213-012-0583-8
   Web of Science ®Google Scholar
• Stanley, A., Punil Kumar, H. N., Mutturi, S., & Vijayendra, S. V. (2018). Fed-batch strategies for production of PHA using a native isolate of Halomonas venusta KT832796 strain. Applied Biochemistry and Biotechnology, 184(3), 935–952. https://doi.org/10.1007/s12010-017-2601-6
   PubMed Web of Science ®Google Scholar
• Tanimura, K., Matsumoto, T., Nakayama, H., Tanaka, T., & Kondo, A. (2016). Improvement of ectoine productivity by using sugar transporter-overexpressing Halomonas elongata. Enzyme and Microbial Technology, 89, 63–68. https://doi.org/10.1016/j.enzmictec.2016.03.006
   PubMed Web of Science ®Google Scholar
• Thomas, T., Sudesh, K., Bazire, A., Elain, A., Tan, H. T., Lim, H., & Bruzaud, S. (2020). PHA production and PHA synthases of the halophilic bacterium Halomonas sp. SF2003. Bioengineering, 7(1), 29. https://doi.org/10.3390/bioengineering7010029
   PubMed Web of Science ®Google Scholar
• Tsuji, A., Takei, Y., & Azuma, Y. (2022). Establishment of genetic tools for genomic DNA engineering of Halomonas sp. KM-1, a bacterium with potential for biochemical production. Microbial Cell Factories, 21(1), 122. https://doi.org/10.1186/s12934-022-01797-2
   PubMed Web of Science ®Google Scholar
• Velmurugan, S., Raman, K., Viji, V. T., Donio, M. B. S., Jenifer, J. A., Babu, M. M., & Citarasu, T. (2013). Screening and characterization of antimicrobial secondary metabolites from Halomonas salifodinae MPM-TC and its in vivo antiviral influence on Indian white shrimp Fenneropenaeus indicus against WSSV challenge. Journal of King Saud University-Science, 25(3), 181–190. https://doi.org/10.1016/j.jksus.2013.03.002
   Google Scholar
• Vijayaraghavan, K., Lee, M. W., & Yun, Y. S. (2008). A new approach to study the decolorization of complex reactive dye bath effluent by biosorption technique. Bioresource Technology, 99(13), 5778–5785. https://doi.org/10.1016/j.biortech.2007.10.012
   PubMed Web of Science ®Google Scholar
• Vreeland, R. H., Litchfield, C. D., Martin, E. L., & Eliot, E. (1980). Halomonas elongata, a new genus and species of extremely salt-tolerant bacteria. International Journal of Systematic Bacteriology, 30(2), 485–495. https://doi.org/10.1099/00207713-30-2-485
   Google Scholar
• Vyrides, I., Agathangelou, M., Dimitriou, R., Souroullas, K., Salamex, A., Ioannou, A., & Koutinas, M. (2015). Novel Halomonas sp. B15 isolated from Larnaca Salt Lake in Cyprus that generates vanillin and vanillic acid from ferulic acid. World Journal of Microbiology & Biotechnology, 31(8), 1291–1296. https://doi.org/10.1007/s11274-015-1876-4
   PubMed Web of Science ®Google Scholar
• Wang, T., Li, J., Zhang, L. H., Yu, Y., & Zhu, Y. M. (2017). Simultaneous heterotrophic nitrification and aerobic denitrification at high concentrations of NaCl and ammonia nitrogen by Halomonas bacteria. Water Science and Technology, 76(2), 386–395. https://doi.org/10.2166/wst.2017.214
   PubMed Web of Science ®Google Scholar
• Wohlfarth, A., Severin, J., & Galinski, E. A. (1990). The spectrum of compatible solutes in heterotrophic halophilic eubacteria of the family Halomonadaceae. Journal of General Microbiology, 136(4), 705–712. https://doi.org/10.1099/00221287-136-4-705
   Google Scholar
• Yang, C., Wang, Z., Li, Y., Niu, Y., Du, M., He, X., Ma, C., Tang, H., & Xu, P. (2010). Metabolic versatility of halotolerant and alkaliphilic strains of Halomonas isolated from alkaline black liquor. Bioresource Technology, 101(17), 6778–6784. https://doi.org/10.1016/j.biortech.2010.03.108
   PubMed Web of Science ®Google Scholar
• Yoo, W., Kim, B., Jeon, S., Kim, K. K., & Kim, T. D. (2020). Identification, characterization, and immobilization of a novel YbfF esterase from Halomonas elongata. International Journal of Biological Macromolecules, 165, 1139–1148. https://doi.org/10.1016/j.ijbiomac.2020.09.247
   PubMed Web of Science ®Google Scholar
• Zhang, J., Jin, B., Hong, K., Lv, Y., Wang, Z., & Chen, T. (2021). Cell catalysis of citrate to itaconate by engineered Halomonas bluephagenesis. ACS Synthetic Biology, 10(11), 3017–3027. https://doi.org/10.1021/acssynbio.1c00320
   PubMed Web of Science ®Google Scholar
• Zhao, Q., Li, S., Lv, P., Sun, S., Ma, C., Xu, P., Su, H., & Yang, C. (2019). High ectoine production by an engineered Halomonas hydrothermalis Y2 in a reduced salinity medium. Microbial Cell Factories, 18(1), 1–12. https://doi.org/10.1186/s12934-019-1230-x
   PubMed Web of Science ®Google Scholar