Comparison of bacterial communities associated with Prorocentrum donghaiense and Karenia mikimotoi strains from Chinese coastal waters
Ruoyu Guo A , Pengbin Wang
A B C , Douding Lu A and Xinfeng Dai A C
+ Author Affiliations
- Author Affiliations
A Key Laboratory of Marine Ecosystem Dynamics, Second Institute of Oceanography, Ministry of Natural Resources, 36 Baochubei Road, Hangzhou, 310012, PR China.
B Fourth Institute of Oceanography, Ministry of Natural Resources, 26 New Century Avenue, Beihai, 536000, PR China.
C Corresponding authors. Email: algae@sio.org.cn; xinfengdai@sio.org.cn
Marine and Freshwater Research 71(12) 1662-1671 https://doi.org/10.1071/MF20035
Submitted: 6 February 2020 Accepted: 23 June 2020 Published: 27 August 2020
Abstract
The dinoflagellates Karenia mikimotoi (toxic) and Prorocentrum donghaiense (non-toxic) have caused serious blooms in Chinese coastal waters. Although many studies have investigated the mechanisms underlying the harmful algal blooms of these two species, research on bacterial communities associated with K. mikimotoi and P. donghaiense is still limited. In this study, the composition of associated bacterial communities of K. mikimotoi and P. donghaiense were investigated in cultured strains. The genera with the highest relative abundance in K. mikimotoi and P. donghaiense cultures were Balneola and Marinobacter respectively. There were 26 genera specifically present in K. mikimotoi cultures, including Alteromonas, Methylophaga and Thalassospira. Sixteen genera were specifically present in P. donghaiense cultures, including an unclassified genus belonging to Nannocystaceae, Loktanella and Roseivirga. Various aromatic hydrocarbons capable of degrading bacteria were detected in the K. mikimotoi culture, but not in the P. donghaiense culture; this may contribute to the toxicity or toxin synthesis of K. mikimotoi. The results of this study provide further insights into bloom formation mechanisms and elucidate the different characteristics of K. mikimotoi and P. donghaiense blooms.
References
Aharonovich, D., and Sher, D. (2016). Transcriptional response of Prochlorococcus to co-culture with a marine Alteromonas: differences between strains and the involvement of putative infochemicals. The ISME Journal 10, 2892–2906.| Transcriptional response of Prochlorococcus to co-culture with a marine Alteromonas: differences between strains and the involvement of putative infochemicals.Crossref | GoogleScholarGoogle Scholar | 27128996PubMed |
Amin, S. A., Green, D. H., Hart, M. C., Kupper, F. C., Sunda, W. G., and Carrano, C. J. (2009). Photolysis of iron-siderophore chelates promotes bacterial–algal mutualism. Proceedings of the National Academy of Sciences of the United States of America 106, 17071–17076.
| Photolysis of iron-siderophore chelates promotes bacterial–algal mutualism.Crossref | GoogleScholarGoogle Scholar | 19805106PubMed |
Amin, S. A., Parker, M. S., and Armbrust, E. V. (2012). Interactions between diatoms and bacteria. Microbiology and Molecular Biology Reviews 76, 667–684.
| Interactions between diatoms and bacteria.Crossref | GoogleScholarGoogle Scholar | 22933565PubMed |
Amin, S. A., Hmelo, L. R., van Tol, H. M., Durham, B. P., Carlson, L. T., Heal, K. R., Morales, R. L., Berthiaume, C. T., Parker, M. S., Djunaedi, B., Ingalls, A. E., Parsek, M. R., Moran, M. A., and Armbrust, E. V. (2015). Interaction and signalling between a cosmopolitan phytoplankton and associated bacteria. Nature 522, 98–101.
| Interaction and signalling between a cosmopolitan phytoplankton and associated bacteria.Crossref | GoogleScholarGoogle Scholar | 26017307PubMed |
Anderson, D. M., Cembella, A. D., and Hallegraeff, G. M. (2012). Progress in understanding harmful algal blooms: paradigm shifts and new technologies for research, monitoring, and management. Annual Review of Marine Science 4, 143–176.
| Progress in understanding harmful algal blooms: paradigm shifts and new technologies for research, monitoring, and management.Crossref | GoogleScholarGoogle Scholar | 22457972PubMed |
Bertrand, E. M., McCrow, J. P., Moustafa, A., Zheng, H., McQuaid, J. B., Delmont, T. O., Post, A. F., Sipler, R. E., Spackeen, J. L., Xu, K., Bronk, D. A., Hutchins, D. A., and Allen, A. E. (2015). Phytoplankton–bacterial interactions mediate micronutrient colimitation at the coastal Antarctic sea ice edge. Proceedings of the National Academy of Sciences of the United States of America 112, 9938–9943.
| Phytoplankton–bacterial interactions mediate micronutrient colimitation at the coastal Antarctic sea ice edge.Crossref | GoogleScholarGoogle Scholar | 26221022PubMed |
Bloh, A. H., Usup, G., and Ahmad, A. (2016). Loktanella spp. Gb03 as an algicidal bacterium, isolated from the culture of dinoflagellate Gambierdiscus belizeanus. Veterinary World 9, 142–146.
| Loktanella spp. Gb03 as an algicidal bacterium, isolated from the culture of dinoflagellate Gambierdiscus belizeanus.Crossref | GoogleScholarGoogle Scholar | 27051199PubMed |
Bolch, C. J. S., Bejoy, T. A., and Green, D. H. (2017). Bacterial associates modify growth dynamics of the dinoflagellate Gymnodinium catenatum. Frontiers in Microbiology 8, 670.
| Bacterial associates modify growth dynamics of the dinoflagellate Gymnodinium catenatum.Crossref | GoogleScholarGoogle Scholar |
Bolger, A. M., Lohse, M., and Usadel, B. (2014). Trimmomatic: a flexible trimmer for Illumina sequence data. Bioinformatics 30, 2114–2120.
| Trimmomatic: a flexible trimmer for Illumina sequence data.Crossref | GoogleScholarGoogle Scholar | 24695404PubMed |
Boopathi, T., Faria, D. G., Lee, M. D., Lee, J., Chang, M., and Ki, J. S. (2015). A molecular survey of freshwater microeukaryotes in an Arctic reservoir (Svalbard, 79°N) in summer by using next-generation sequencing. Polar Biology 38, 179–187.
| A molecular survey of freshwater microeukaryotes in an Arctic reservoir (Svalbard, 79°N) in summer by using next-generation sequencing.Crossref | GoogleScholarGoogle Scholar |
Buchan, A., LeCleir, G. R., Gulvik, C. A., and Gonzalez, J. M. (2014). Master recyclers: features and functions of bacteria associated with phytoplankton blooms. Nature Reviews. Microbiology 12, 686–698.
| Master recyclers: features and functions of bacteria associated with phytoplankton blooms.Crossref | GoogleScholarGoogle Scholar | 25134618PubMed |
Chang, F. H., Zeldis, J., Gall, M., and Hall, J. (2003). Seasonal and spatial variation of phytoplankton assemblages, biomass and cell size from spring to summer across the north-eastern New Zealand continental shelf. Journal of Plankton Research 25, 737–758.
| Seasonal and spatial variation of phytoplankton assemblages, biomass and cell size from spring to summer across the north-eastern New Zealand continental shelf.Crossref | GoogleScholarGoogle Scholar |
Croft, M. T., Lawrence, A. D., Raux-Deery, E., Warren, M. J., and Smith, A. G. (2005). Algae acquire vitamin B12 through a symbiotic relationship with bacteria. Nature 438, 90–93.
| Algae acquire vitamin B12 through a symbiotic relationship with bacteria.Crossref | GoogleScholarGoogle Scholar | 16267554PubMed |
Cruz-López, R., and Maske, H. (2016). The vitamin B1 and B12 required by the marine dinoflagellate Lingulodinium polyedrum can be provided by its associated bacterial community in culture. Frontiers in Microbiology 7, 560.
| The vitamin B1 and B12 required by the marine dinoflagellate Lingulodinium polyedrum can be provided by its associated bacterial community in culture.Crossref | GoogleScholarGoogle Scholar | 27199906PubMed |
Dang, L. X., Li, Y., Liu, F., Zhang, Y., Yang, W. D., Li, H. Y., and Liu, J. S. (2015). Chemical response of the toxic dinoflagellate Karenia mikimotoi against grazing by three species of zooplankton. The Journal of Eukaryotic Microbiology 62, 470–480.
| Chemical response of the toxic dinoflagellate Karenia mikimotoi against grazing by three species of zooplankton.Crossref | GoogleScholarGoogle Scholar | 25523905PubMed |
Demuez, M., Gonzalez-Fernandez, C., and Ballesteros, M. (2015). Algicidal microorganisms and secreted algicides: new tools to induce microalgal cell disruption. Biotechnology Advances 33, 1615–1625.
| Algicidal microorganisms and secreted algicides: new tools to induce microalgal cell disruption.Crossref | GoogleScholarGoogle Scholar | 26303095PubMed |
Edgar, R. C. (2010). Search and clustering orders of magnitude faster than BLAST. Bioinformatics 26, 2460.
| Search and clustering orders of magnitude faster than BLAST.Crossref | GoogleScholarGoogle Scholar | 20709691PubMed |
Fandino, L. B., Riemann, L., Steward, G. F., Long, R. A., and Azam, F. (2001). Variations in bacterial community structure during a dinoflagellate bloom. Aquatic Microbial Ecology 23, 119–130.
| Variations in bacterial community structure during a dinoflagellate bloom.Crossref | GoogleScholarGoogle Scholar |
Fernández-Gómez, B., Richter, M., Schuler, M., Pinhassi, J., Acinas, S. G., Gonzalez, J. M., and Pedros-Alio, C. (2013). Ecology of marine Bacteroidetes: a comparative genomics approach. The ISME Journal 7, 1026–1037.
| Ecology of marine Bacteroidetes: a comparative genomics approach.Crossref | GoogleScholarGoogle Scholar | 23303374PubMed |
Garson, M. J. (2001). Ecological perspectives on marine natural product biosynthesis. In ‘Marine Chemical Ecology’. (Eds J. B. McClintock and B. J. Baker.) pp 75–80. (CRC Press: Boca Raton, FL, USA.)
Green, D. H., Llewellyn, L. E., Negri, A. P., Blackburn, S. I., and Bolch, C. J. S. (2004). Phylogenetic and functional diversity of the cultivable bacterial community associated with the paralytic shellfish poisoning dinoflagellate Gymnodinium catenatum. FEMS Microbiology Ecology 47, 345–357.
| Phylogenetic and functional diversity of the cultivable bacterial community associated with the paralytic shellfish poisoning dinoflagellate Gymnodinium catenatum.Crossref | GoogleScholarGoogle Scholar | 19712323PubMed |
Gutierrez, T., Nichols, P. D., Whitman, W. B., and Aitken, M. D. (2012). Porticoccus hydrocarbonoclasticus sp. nov., an aromatic hydrocarbon-degrading bacterium identified in laboratory cultures of marine phytoplankton. Applied and Environmental Microbiology 78, 628–637.
| Porticoccus hydrocarbonoclasticus sp. nov., an aromatic hydrocarbon-degrading bacterium identified in laboratory cultures of marine phytoplankton.Crossref | GoogleScholarGoogle Scholar | 22139001PubMed |
Hennon, G. M., Morris, J. J., Haley, S. T., Zinser, E. R., Durrant, A. R., Entwistle, E., Dokland, T., and Dyhrman, S. T. (2018). The impact of elevated CO2 on Prochlorococcus and microbial interactions with ‘helper’ bacterium Alteromonas. The ISME Journal 12, 520–531.
| The impact of elevated CO2 on Prochlorococcus and microbial interactions with ‘helper’ bacterium Alteromonas.Crossref | GoogleScholarGoogle Scholar |
Landa, M., Blain, S., Harmand, J., Monchy, S., Rapaport, A., and Obernosterer, I. (2018). Major changes in the composition of a Southern Ocean bacterial community in response to diatom-derived dissolved organic matter. FEMS Microbiology Ecology 94, fiy067.
| Major changes in the composition of a Southern Ocean bacterial community in response to diatom-derived dissolved organic matter.Crossref | GoogleScholarGoogle Scholar | 29931341PubMed |
Lawson, C. A., Raina, J. B., Kahlke, T., Seymour, J. R., and Suggett, D. J. (2018). Defining the core microbiome of the symbiotic dinoflagellate, Symbiodinium. Environmental Microbiology Reports 10, 7–11.
| Defining the core microbiome of the symbiotic dinoflagellate, Symbiodinium.Crossref | GoogleScholarGoogle Scholar | 29124895PubMed |
Li, D.-X., Zhang, H., Chen, X.-H., Xie, Z.-X., Zhang, Y., Zhang, S.-F., Lin, L., Chen, F., and Wang, D.-Z. (2018). Metaproteomics reveals major microbial players and their metabolic activities during the blooming period of a marine dinoflagellate Prorocentrum donghaiense. Environmental Microbiology 20, 632–644.
| Metaproteomics reveals major microbial players and their metabolic activities during the blooming period of a marine dinoflagellate Prorocentrum donghaiense.Crossref | GoogleScholarGoogle Scholar | 29124849PubMed |
Li, X., Yan, T., Yu, R., and Zhou, M. (2019). A review of Karenia mikimotoi: bloom events, physiology, toxicity and toxic mechanism. Harmful Algae 90, 101702.
| A review of Karenia mikimotoi: bloom events, physiology, toxicity and toxic mechanism.Crossref | GoogleScholarGoogle Scholar | 31806160PubMed |
Lo, N., Kang, H. J., and Jeon, C. O. (2014). Zhongshania aliphaticivorans sp. nov., an aliphatic hydrocarbon-degrading bacterium isolated from marine sediment, and transfer of Spongiibacter borealis Jang et al. 2011 to the genus Zhongshania as Zhongshania borealis comb. nov. International Journal of Systematic and Evolutionary Microbiology 64, 3768–3774.
| Zhongshania aliphaticivorans sp. nov., an aliphatic hydrocarbon-degrading bacterium isolated from marine sediment, and transfer of Spongiibacter borealis Jang et al. 2011 to the genus Zhongshania as Zhongshania borealis comb. nov.Crossref | GoogleScholarGoogle Scholar | 25122615PubMed |
Lu, D., Goebel, J., Qi, Y., Zou, J., Han, X., Gao, Y., and Li, Y. (2005). Morphological and genetic study of Prorocentrum donghaiense Lu from the East China Sea, and comparison with some related Prorocentrum species. Harmful Algae 4, 493–505.
| Morphological and genetic study of Prorocentrum donghaiense Lu from the East China Sea, and comparison with some related Prorocentrum species.Crossref | GoogleScholarGoogle Scholar |
Lu, D., Wang, H., Huang, H., Xia, P., Dai, X.-F., Gobel, J., and Jeong, H.-J. (2011). Morphological and genetic comparison of two strains of a Prorocentrum species isolated from Zhejiang coastal water of China and Masan Bay of Korea. Chinese Journal of Oceanology and Limnology 29, 832–839.
| Morphological and genetic comparison of two strains of a Prorocentrum species isolated from Zhejiang coastal water of China and Masan Bay of Korea.Crossref | GoogleScholarGoogle Scholar |
Lupette, J., Lami, R., Krasovec, M., Grimsley, N., Moreau, H., Piganeau, G., and Sanchez-Ferandin, S. (2016). Marinobacter dominates the bacterial community of the Ostreococcus tauri phycosphere in culture. Frontiers in Microbiology 7, 1414.
| Marinobacter dominates the bacterial community of the Ostreococcus tauri phycosphere in culture.Crossref | GoogleScholarGoogle Scholar | 27656176PubMed |
Magoc, T., and Salzberg, S. L. (2011). FLASH: fast length adjustment of short reads to improve genome assemblies. Bioinformatics 27, 2957–2963.
| FLASH: fast length adjustment of short reads to improve genome assemblies.Crossref | GoogleScholarGoogle Scholar | 21903629PubMed |
Mayali, X., and Azam, F. (2004). Algicidal bacteria in the sea and their impact on algal blooms. The Journal of Eukaryotic Microbiology 51, 139–144.
| Algicidal bacteria in the sea and their impact on algal blooms.Crossref | GoogleScholarGoogle Scholar | 15134248PubMed |
Mayali, X., Franks, P. J. S., and Burton, R. S. (2011). Temporal attachment dynamics by distinct bacterial taxa during a dinoflagellate bloom. Aquatic Microbial Ecology 63, 111–122.
| Temporal attachment dynamics by distinct bacterial taxa during a dinoflagellate bloom.Crossref | GoogleScholarGoogle Scholar |
Mishamandani, S., Gutierrez, T., and Aitken, M. D. (2014). DNA-based stable isotope probing coupled with cultivation methods implicates Methylophaga in hydrocarbon degradation. Frontiers in Microbiology 5, 76.
| DNA-based stable isotope probing coupled with cultivation methods implicates Methylophaga in hydrocarbon degradation.Crossref | GoogleScholarGoogle Scholar | 24578702PubMed |
Mishamandani, S., Gutierrez, T., Berry, D., and Aitken, M. D. (2016). Response of the bacterial community associated with a cosmopolitan marine diatom to crude oil shows a preference for the biodegradation of aromatic hydrocarbons. Environmental Microbiology 18, 1817–1833.
| Response of the bacterial community associated with a cosmopolitan marine diatom to crude oil shows a preference for the biodegradation of aromatic hydrocarbons.Crossref | GoogleScholarGoogle Scholar | 26184578PubMed |
Neufeld, J. D., Boden, R., Moussard, H., Schäfer, H., and Murrell, J. C. (2008). Substrate-specific clades of active marine methylotrophs associated with a phytoplankton bloom in a temperate coastal environment. Applied and Environmental Microbiology 74, 7321–7328.
| Substrate-specific clades of active marine methylotrophs associated with a phytoplankton bloom in a temperate coastal environment.Crossref | GoogleScholarGoogle Scholar | 18849453PubMed |
Oh, C., Heo, S. J., De Zoysa, M., Affan, A., Jung, W. K., Park, H. S., Lee, Y., Lee, J., Yoon, K. T., and Kang, D. H. (2011). Whole-genome sequence of the xylanase-producing Mesoflavibacter zeaxanthinifaciens strain S86. Journal of Bacteriology 193, 5557.
| Whole-genome sequence of the xylanase-producing Mesoflavibacter zeaxanthinifaciens strain S86.Crossref | GoogleScholarGoogle Scholar | 21914876PubMed |
Ohkubo, N., Tomaru, Y., Yamaguchi, H., Kitatsuji, S., and Mochida, K. (2017). Development of a method to assess the ichthyotoxicity of the harmful marine microalgae Karenia spp. using gill cell cultures from red sea bream (Pagrus major). Fish Physiology and Biochemistry 43, 1603–1612.
| Development of a method to assess the ichthyotoxicity of the harmful marine microalgae Karenia spp. using gill cell cultures from red sea bream (Pagrus major).Crossref | GoogleScholarGoogle Scholar | 28695381PubMed |
Okai, M., Kihara, I., Yokoyama, Y., Ishida, M., and Urano, N. (2015). Isolation and characterization of benzo[a]pyrene-degrading bacteria from the Tokyo Bay area and Tama River in Japan. FEMS Microbiology Letters 362, fnv143.
| Isolation and characterization of benzo[a]pyrene-degrading bacteria from the Tokyo Bay area and Tama River in Japan.Crossref | GoogleScholarGoogle Scholar | 26316544PubMed |
Park, B. S., Guo, R., Lim, W.-A., and Ki, J.-S. (2017). Pyrosequencing reveals specific associations of bacterial clades Roseobacter and Flavobacterium with the harmful dinoflagellate Cochlodinium polykrikoides growing in culture. Marine Ecology (Berlin) 38, e12474.
| Pyrosequencing reveals specific associations of bacterial clades Roseobacter and Flavobacterium with the harmful dinoflagellate Cochlodinium polykrikoides growing in culture.Crossref | GoogleScholarGoogle Scholar |
Park, B. S., Guo, R., Lim, W. A., and Ki, J. S. (2018). Importance of free-living and particle-associated bacteria for the growth of the harmful dinoflagellate Prorocentrum minimum: evidence in culture stages. Marine and Freshwater Research 69, 290–299.
| Importance of free-living and particle-associated bacteria for the growth of the harmful dinoflagellate Prorocentrum minimum: evidence in culture stages.Crossref | GoogleScholarGoogle Scholar |
Pinhassi, J., Sala, M. M., Havskum, H., Peters, F., Guadayol, O., Malits, A., and Marrasé, C. (2004). Changes in bacterioplankton composition under different phytoplankton regimens. Applied and Environmental Microbiology 70, 6753–6766.
| Changes in bacterioplankton composition under different phytoplankton regimens.Crossref | GoogleScholarGoogle Scholar | 15528542PubMed |
Quast, C., Pruesse, E., Yilmaz, P., Gerken, J., Schweer, T., Yarza, P., Peplies, J., and Glöckner, F. O. (2013). The SILVA ribosomal RNA gene database project: improved data processing and web-based tools. Nucleic Acids Research 41, D590–D596.
| The SILVA ribosomal RNA gene database project: improved data processing and web-based tools.Crossref | GoogleScholarGoogle Scholar | 23193283PubMed |
Ramanan, R., Kim, B. H., Cho, D. H., Oh, H. M., and Kim, H. S. (2016). Algae–bacteria interactions: evolution, ecology and emerging applications. Biotechnology Advances 34, 14–29.
| Algae–bacteria interactions: evolution, ecology and emerging applications.Crossref | GoogleScholarGoogle Scholar | 26657897PubMed |
Reintjes, G., Arnosti, C., Fuchs, B. M., and Amann, R. (2017). An alternative polysaccharide uptake mechanism of marine bacteria. The ISME Journal 11, 1640–1650.
| An alternative polysaccharide uptake mechanism of marine bacteria.Crossref | GoogleScholarGoogle Scholar | 28323277PubMed |
Rink, B., Seeberger, S., Martens, T., Duerselen, C.-D., Simon, M., and Brinkhoff, T. (2007). Effects of phytoplankton bloom in a coastal ecosystem on the composition of bacterial communities. Aquatic Microbial Ecology 48, 47–60.
| Effects of phytoplankton bloom in a coastal ecosystem on the composition of bacterial communities.Crossref | GoogleScholarGoogle Scholar |
Sharma, G., Khatri, I., and Subramanian, S. (2016). Complete genome of the starch-degrading Myxobacteria Sandaracinus amylolyticus DSM 53668T. Genome Biology and Evolution 8, 2520–2529.
| Complete genome of the starch-degrading Myxobacteria Sandaracinus amylolyticus DSM 53668T.Crossref | GoogleScholarGoogle Scholar | 27358428PubMed |
Shi, R., Huang, H., Qi, Z., Hu, W., Tian, Z., and Dai, M. (2013). Algicidal activity against Skeletonema costatum by marine bacteria isolated from a high frequency harmful algal blooms area in southern Chinese coast. World Journal of Microbiology & Biotechnology 29, 153–162.
| Algicidal activity against Skeletonema costatum by marine bacteria isolated from a high frequency harmful algal blooms area in southern Chinese coast.Crossref | GoogleScholarGoogle Scholar |
Shi, X., Liu, L., Li, Y., Xiao, Y., Ding, G., Lin, S., and Chen, J. (2018). Isolation of an algicidal bacterium and its effects against the harmful-algal-bloom dinoflagellate Prorocentrum donghaiense (Dinophyceae). Harmful Algae 80, 72–79.
| Isolation of an algicidal bacterium and its effects against the harmful-algal-bloom dinoflagellate Prorocentrum donghaiense (Dinophyceae).Crossref | GoogleScholarGoogle Scholar | 30502814PubMed |
Suleiman, M., Zecher, K., Yucel, O., Jagmann, N., and Philipp, B. (2016). Interkingdom cross-feeding of ammonium from marine methylamine-degrading bacteria to the diatom Phaeodactylum tricornutum. Applied and Environmental Microbiology 82, 7113–7122.
| Interkingdom cross-feeding of ammonium from marine methylamine-degrading bacteria to the diatom Phaeodactylum tricornutum.Crossref | GoogleScholarGoogle Scholar | 27694241PubMed |
Teeling, H., Fuchs, B. M., Becher, D., Klockow, C., Gardebrecht, A., Bennke, C. M., Kassabgy, M., Huang, S., Mann, A. J., Waldmann, J., Weber, M., Klindworth, A., Otto, A., Lange, J., Bernhardt, J., Reinsch, C., Hecker, M., Peplies, J., Bockelmann, F. D., Callies, U., Gerdts, G., Wichels, A., Wiltshire, K. H., Glockner, F. O., Schweder, T., and Amann, R. (2012). Substrate-controlled succession of marine bacterioplankton populations induced by a phytoplankton bloom. Science 336, 608–611.
| Substrate-controlled succession of marine bacterioplankton populations induced by a phytoplankton bloom.Crossref | GoogleScholarGoogle Scholar | 22556258PubMed |
Thompson, H., Angelova, A., Bowler, B., Jones, M., and Gutierrez, T. (2017). Enhanced crude oil biodegradative potential of natural phytoplankton-associated hydrocarbonoclastic bacteria. Environmental Microbiology 19, 2843–2861.
| Enhanced crude oil biodegradative potential of natural phytoplankton-associated hydrocarbonoclastic bacteria.Crossref | GoogleScholarGoogle Scholar | 28585283PubMed |
Uribe-Flores, M. M., Cerqueda-Garcia, D., Hernandez-Nunez, E., Cadena, S., Garcia-Cruz, N. U., Trejo-Hernandez, M. R., Aguirre-Macedo, M. L., and Garcia-Maldonado, J. Q. (2019). Bacterial succession and co-occurrence patterns of an enriched marine microbial community during light crude oil degradation in a batch reactor. Journal of Applied Microbiology 127, 495–507.
| Bacterial succession and co-occurrence patterns of an enriched marine microbial community during light crude oil degradation in a batch reactor.Crossref | GoogleScholarGoogle Scholar | 31077511PubMed |
Wang, K., and Brown, R. C. (2013). Catalytic pyrolysis of microalgae for production of aromatics and ammonia. Green Chemistry 15, 675.
| Catalytic pyrolysis of microalgae for production of aromatics and ammonia.Crossref | GoogleScholarGoogle Scholar |
Wang, C., Lin, X., Li, L., Lin, L., and Lin, S. (2017). Glyphosate shapes a dinoflagellate-associated bacterial community while supporting algal growth as sole phosphorus source. Frontiers in Microbiology 8, 2530.
| Glyphosate shapes a dinoflagellate-associated bacterial community while supporting algal growth as sole phosphorus source.Crossref | GoogleScholarGoogle Scholar | 29312222PubMed |
Wang, P., Joo, J.-H., Park, B. S., Kim, J.-H., Kim, J. H., and Han, M.-S. (2017b). Relationship between dissolved organic carbon and bacterial community in the coastal waters of Incheon, Korea. Oceanological and Hydrobiological Studies 46, 50–61.
| Relationship between dissolved organic carbon and bacterial community in the coastal waters of Incheon, Korea.Crossref | GoogleScholarGoogle Scholar |
Wang, H., Niu, X., Feng, X., Goncalves, R. J., and Guan, W. (2019a). Effects of ocean acidification and phosphate limitation on physiology and toxicity of the dinoflagellate Karenia mikimotoi. Harmful Algae 87, 101621.
| Effects of ocean acidification and phosphate limitation on physiology and toxicity of the dinoflagellate Karenia mikimotoi.Crossref | GoogleScholarGoogle Scholar | 31349890PubMed |
Wang, P., Dai, X.-F., and Lu, D.-D. (2019b). Co-culture bacterial community of Karenia mikimotoi (KM-02). Oceanologia et Limnologia Sinica 50, 644–651.
| Co-culture bacterial community of Karenia mikimotoi (KM-02).Crossref | GoogleScholarGoogle Scholar |
Wietz, M., Wemheuer, B., Simon, H., Giebel, H. A., Seibt, M. A., Daniel, R., Brinkhoff, T., and Simon, M. (2015). Bacterial community dynamics during polysaccharide degradation at contrasting sites in the Southern and Atlantic Oceans. Environmental Microbiology 17, 3822–3831.
| Bacterial community dynamics during polysaccharide degradation at contrasting sites in the Southern and Atlantic Oceans.Crossref | GoogleScholarGoogle Scholar | 25753990PubMed |
Xu, N., Duan, S., Li, A., Zhang, C., Cai, Z., and Hu, Z. (2010). Effects of temperature, salinity and irradiance on the growth of the harmful dinoflagellate Prorocentrum donghaiense Lu. Harmful Algae 9, 13–17.
| Effects of temperature, salinity and irradiance on the growth of the harmful dinoflagellate Prorocentrum donghaiense Lu.Crossref | GoogleScholarGoogle Scholar |
Yang, C., Yi, L., Zhou, B., Zhou, Y., Wei, Z., Yun, T., Nostrand, J. D. V., Wu, L., He, Z., and Zhou, J. (2015). Illumina sequencing-based analysis of free-living bacterial community dynamics during an Akashiwo sanguine bloom in Xiamen sea, China. Scientific Reports 5, 8476.
| Illumina sequencing-based analysis of free-living bacterial community dynamics during an Akashiwo sanguine bloom in Xiamen sea, China.Crossref | GoogleScholarGoogle Scholar | 25684124PubMed |
Yang, S., Li, M., Lai, Q., Li, G., and Shao, Z. (2018). Alcanivorax mobilis sp. nov., a new hydrocarbon-degrading bacterium isolated from deep-sea sediment. International Journal of Systematic and Evolutionary Microbiology 68, 1639–1643.
| Alcanivorax mobilis sp. nov., a new hydrocarbon-degrading bacterium isolated from deep-sea sediment.Crossref | GoogleScholarGoogle Scholar | 29620491PubMed |
Zhou, J., Chen, G. F., Ying, K. Z., Jin, H., Song, J. T., and Cai, Z. H. (2019). Phycosphere microbial succession patterns and assembly mechanisms in a marine dinoflagellate bloom. Applied and Environmental Microbiology 85, e00349-19.
| Phycosphere microbial succession patterns and assembly mechanisms in a marine dinoflagellate bloom.Crossref | GoogleScholarGoogle Scholar | 31540986PubMed |
Zou, Y., Yamasaki, Y., Matsuyama, Y., Yamaguchi, K., Honjo, T., and Oda, T. (2010). Possible involvement of hemolytic activity in the contact-dependent lethal effects of the dinoflagellate Karenia mikimotoi on the rotifer Brachionus plicatilis. Harmful Algae 9, 367–373.
| Possible involvement of hemolytic activity in the contact-dependent lethal effects of the dinoflagellate Karenia mikimotoi on the rotifer Brachionus plicatilis.Crossref | GoogleScholarGoogle Scholar |
