Journal articles: 'Marine microbiology'

1

Finlay, B. J., and B. Austin. "Marine Microbiology." Journal of Animal Ecology 58, no. 2 (June 1989): 727. http://dx.doi.org/10.2307/4859.

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Bunt, J. S. "Marine microbiology." Aquatic Botany 36, no. 1 (December 1989): 103–5. http://dx.doi.org/10.1016/0304-3770(89)90098-3.

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3

Wakefield, S. J. "Marine microbiology." Endeavour 14, no. 2 (January 1990): 102. http://dx.doi.org/10.1016/0160-9327(90)90095-9.

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4

Yayanos, Aristides. "Marine Microbiology at Scripps." Oceanography 16, no. 3 (2003): 67–75. http://dx.doi.org/10.5670/oceanog.2003.33.

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5

Fenchel, Tom. "Marine Microbiology. B. Austin." Quarterly Review of Biology 64, no. 3 (September 1989): 357. http://dx.doi.org/10.1086/416416.

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Thomas Millington, J., and Peggt Wilhelm. "Marine microbiology of Rocas Alijos." Journal of Wilderness Medicine 4, no. 4 (November 1993): 384–90. http://dx.doi.org/10.1580/0953-9859-4.4.384.

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7

Lane, Nick. "Marine microbiology: Origins of Death." Nature 453, no. 7195 (May 2008): 583–85. http://dx.doi.org/10.1038/453583a.

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8

Gram, Lone. "Microbiology of marine food products." Trends in Food Science & Technology 2 (January 1991): 259–60. http://dx.doi.org/10.1016/0924-2244(91)90711-q.

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Hobbs, G. "Microbiology of marine food products." Fisheries Research 12, no. 2 (October 1991): 183–84. http://dx.doi.org/10.1016/0165-7836(91)90042-e.

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10

MacLeod, Robert A. "Marine Microbiology Far From the Sea." Annual Review of Microbiology 39, no. 1 (October 1985): 1–21. http://dx.doi.org/10.1146/annurev.mi.39.100185.000245.

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11

KOGURE, KAZUTAKA. "On future image of marine microbiology." Bulletin of Japanese Society of Microbial Ecology 5, no. 2 (1990): 45–50. http://dx.doi.org/10.1264/microbes1986.5.45.

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12

Wilson, Jean. "Marine microbiology: ecology and applications (2nd Edn)." Journal of Biological Education 46, no. 2 (June 2012): 120. http://dx.doi.org/10.1080/00219266.2011.645856.

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13

Williams, Beth T., and Jonathan D. Todd. "Publisher Correction: Marine microbiology: A day in the life of marine sulfonates." Nature Microbiology 4, no. 12 (October 18, 2019): 2580–81. http://dx.doi.org/10.1038/s41564-019-0606-3.

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HARTZ, AARON J., BARRY F. SHERR, and EVELYN B. SHERR. "Photoresponse in the Heterotrophic Marine Dinoflagellate Oxyrrhis marina." Journal of Eukaryotic Microbiology 58, no. 2 (February 18, 2011): 171–77. http://dx.doi.org/10.1111/j.1550-7408.2011.00529.x.

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15

Mixter, Phil. "A Review of Marine Microbiology: Ecology and Applications." Journal of Microbiology & Biology Education 12, no. 2 (December 1, 2011): 212–13. http://dx.doi.org/10.1128/jmbe.v12i2.336.

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16

Jannasch, Holger W. "Marine Microbiology Microbes in the Sea M. A. Sleigh." BioScience 38, no. 10 (November 1988): 711–12. http://dx.doi.org/10.2307/1310886.

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17

Emerson, David. "Biogeochemistry and microbiology of microaerobic Fe(II) oxidation." Biochemical Society Transactions 40, no. 6 (November 21, 2012): 1211–16. http://dx.doi.org/10.1042/bst20120154.

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Today high Fe(II) environments are relegated to oxic–anoxic habitats with opposing gradients of O2 and Fe(II); however, during the late Archaean and early Proterozoic eons, atmospheric O2 concentrations were much lower and aqueous Fe(II) concentrations were significantly higher. In current Fe(II)-rich environments, such as hydrothermal vents, mudflats, freshwater wetlands or the rhizosphere, rusty mat-like deposits are common. The presence of abundant biogenic microtubular or filamentous iron oxyhydroxides readily reveals the role of FeOB (iron-oxidizing bacteria) in iron mat formation. Cultivation and cultivation-independent techniques, confirm that FeOB are abundant in these mats. Despite remarkable similarities in morphological characteristics between marine and freshwater FeOB communities, the resident populations of FeOB are phylogenetically distinct, with marine populations related to the class Zetaproteobacteria, whereas freshwater populations are dominated by members of the Gallionallaceae, a family within the Betaproteobacteria. Little is known about the mechanism of how FeOB acquire electrons from Fe(II), although it is assumed that it involves electron transfer from the site of iron oxidation at the cell surface to the cytoplasmic membrane. Comparative genomics between freshwater and marine strains reveals few shared genes, except for a suite of genes that include a class of molybdopterin oxidoreductase that could be involved in iron oxidation via extracellular electron transport. Other genes are implicated as well, and the overall genomic analysis reveals a group of organisms exquisitely adapted for growth on iron.

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Dawson, RA, AT Crombie, P. Pichon, M. Steinke, TJ McGenity, and JC Murrell. "The microbiology of isoprene cycling in aquatic ecosystems." Aquatic Microbial Ecology 87 (July 15, 2021): 79–98. http://dx.doi.org/10.3354/ame01972.

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Isoprene (2-methyl-1,3-butadiene) is emitted in vast quantities (>500 Tg C yr-1). Most isoprene is emitted by trees, but there is still incomplete understanding of the diversity of isoprene sources. The reactivity of isoprene in the atmosphere has potential implications for both global warming and global cooling, with human health implications also arising from isoprene-induced ozone formation in urban areas. Isoprene emissions from terrestrial environments have been studied for many years, but our understanding of aquatic isoprene emissions is less complete. Several abundant phytoplankton taxa produced isoprene in the laboratory, and the relationship between chlorophyll a and isoprene production has been used to estimate emissions from marine environments. The aims of this review are to highlight the role of aquatic environments in the biological cycling of isoprene and to stimulate further study of isoprene metabolism in marine and freshwater environments. From a microbial ecology perspective, the isoprene metabolic gene cluster, first identified in Rhodococcus sp. AD45 (isoGHIJABCDEF) and subsequently found in every genome-sequenced isoprene-degrader, provides the ideal basis for molecular studies on the distribution and diversity of isoprene-degrading communities. Further investigations of isoprene-emitting microbes, such as the influence of environmental factors and geographical location, must also be considered when attempting to constrain estimates of the flux of isoprene in aquatic ecosystems. We also report isoprene emission by the scleractinian coral Acropora horrida and the degradation of isoprene by the same coral holobiont, which highlights the importance of better understanding the cycling of isoprene in marine environments.

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Fajarningsih, Nurrahmi Dewi. "AN EMERGING MARINE BIOTECHNOLOGY: MARINE DRUG DISCOVERY." Squalen Bulletin of Marine and Fisheries Postharvest and Biotechnology 7, no. 2 (May 23, 2013): 89. http://dx.doi.org/10.15578/squalen.v7i2.19.

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Marine natural resources offer an opportunity to discover a novel chemical diversity withinterest ing pharmacologically active compounds to treat many diseases such as cancer,inflammation, bacterial and parasitic infections, and many other diseases. Marine drug discoveryis a rising area in marine biotechnology. Several hits of marine-derived drug compounds wereapproved; two of them are Ziconotide and Trabectedin. In 2004, Ziconotide was approved as paintreatment drugs in the United States and Europe. Then, in 2007, Trabectedin was also approvedas anticancer drug in Europe. The main problem in marine drug discovery research is materialsupply problem. Up till now, strategies to overcome the problem are “Pharmaceutical aquaculture”of biologically active marine biota and chemical synthesis approach. Chemical synthesis approachis feasible solution to be used, especially when working with less complex structure of compounds.However, when working with structurally complex compounds where total or even semi synthesiswas very difficult to be provided, aquaculture can be a solution. Currently, the use of microbiology,biochemistry, genetic, bioinformatics, genomic and meta-genomic has been intensifying in orderto have a better result in marine natural product drug discovery. As chemical synthesis needs anexpensive investment of advanced technology and highly skilled human resources, thuspharmaceutical aquaculture is more practicable to overcome the material supply insufficiency inIndonesia. Up till now, many Indonesian marine bioprospectors have been working with culturablemarine microorganism to produce bioactive compounds and some others starting to work withgenomic and metagenomic-based drug discovery.

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Zhang, Yu, Jan B. A. Arends, Tom Van de Wiele, and Nico Boon. "Bioreactor technology in marine microbiology: From design to future application." Biotechnology Advances 29, no. 3 (May 2011): 312–21. http://dx.doi.org/10.1016/j.biotechadv.2011.01.004.

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Christie-Oleza, Joseph A., and Jean Armengaud. "Proteomics of theRoseobacterclade, a window to the marine microbiology landscape." PROTEOMICS 15, no. 23-24 (November 23, 2015): 3928–42. http://dx.doi.org/10.1002/pmic.201500222.

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Kim, Minji, Ki-Eun Lee, In-Tae Cha, Eui Tae Kim, and Soo-Je Park. "Salinimonas marina sp. nov. Isolated from Jeju Island Marine Sediment." Current Microbiology 78, no. 8 (June 25, 2021): 3321–27. http://dx.doi.org/10.1007/s00284-021-02576-9.

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23

Williams, Peter J. le B., and Hugh W. Ducklow. "The microbial loop concept: A history, 1930–1974." Journal of Marine Research 77, no. 2 (December 15, 2019): 23–81. http://dx.doi.org/10.1357/002224019828474359.

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The microbial loop as a leading concept in marine microbiology gained wide recognition in the 1980s, but it has roots extending back to the 1930s when microbiologists first began to take a more dynamic approach to investigating the roles of bacteria in ocean food webs and biogeochemical cycles. Here we present a history of the microbial loop concept with emphasis on the period starting in 1930, when marine bacteriologists in Russia and the West began to study explicitly the roles of marine bacteria in the sea. Selman Waksman at Woods Hole and Claude ZoBell at La Jolla relied on colony counts on agar plates as the basis of their work. We suggest that failure to accept direct microscopic evidence of high numbers of bacteria in seawater retarded conceptual development in the West well into the 1970s. Easterners pioneered direct count and radioisotopic techniques and created a dynamic marine microbiology integrating bacteria as important components of marine food webs by the 1960s. Yurii Sorokin and colleagues carried out extensive experimental studies of bacteria as food for marine grazers and provided data for Mikhail Vinogradov and his group to write the first numerical simulation models of ocean ecosystems incorporating microbial components. It had little impact on the Western modeling community, as other Russian work of the times. In spite of continuing technical shortcomings in the field, Lawrence Pomeroy constructed a new conceptual model, providing a synthesis pointing the way toward a modern view of marine microbial ecology that finally matured technically and conceptually in the West in the early 1980s.

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Silkin, Vladimir A. "The main directions of scientific research in the seas of the Mediterranean basin (Based on materials from the 42nd Congress of CIESM, October 7-11, 2019, Cascais, Portugal)." Hydrosphere Еcology (Экология гидросферы), no. 2(4) (2019): 52–58. http://dx.doi.org/10.33624/2587-9367-2019-2(4)-52-58.

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Based on the proceeding of the 42nd CIESM Congress, reports are considered in such direction as “Physics and Climate of the Ocean”, “Marine Biogeochemistry”, “Marine Microbiology and Biotechnology” and “Biological Resources and Marine Ecosystems”. Compared to the previous congress, the number of sessions has significantly increased, the subject and structure of research have expanded. A large number of reports were presented at such sessions as Microplastic, Bioinvasion. The national structure of participants has changed towards an increase in the share of North African countries.

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25

Mosyagin, Igor G. "Role and place of maritime medicine." Marine Medicine 9, no. 3 (November 20, 2023): 7–12. http://dx.doi.org/10.22328/2413-5747-2023-9-3-7-12.

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The article considers the role and place of maritime medicine as science, as a separate health care industry and as the academic discipline. Maritime medicine is at the crossroads of 2 vast areas of human knowledge – medicine and oceanology. As medical science, maritime medicine explores the impact of Ocean on human health in order to develop means and methods of preserving the Earth’s human potential, first of all, the one of maritime industry and coastal territories. Maritime medicine includes a set of private medical sciences, such as marine hygiene, marine epidemiology, medicine for ships, diving medicine, naval medicine, marine ergonomics, marine physiology and pathophysiology, marine therapy, marine surgery, marine toxicology, marine pharmacy, history of marine medicine, marine health care organizations and some other disciplines. The article discusses the relationship of maritime medicine with other fields of knowledge, sciences and academic disciplines.

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Numberger, Daniela, Ursula Siebert, Marcus Fulde, and Peter Valentin-Weigand. "Streptococcal Infections in Marine Mammals." Microorganisms 9, no. 2 (February 10, 2021): 350. http://dx.doi.org/10.3390/microorganisms9020350.

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Marine mammals are sentinels for the marine ecosystem and threatened by numerous factors including infectious diseases. One of the most frequently isolated bacteria are beta-hemolytic streptococci. However, knowledge on ecology and epidemiology of streptococcal species in marine mammals is very limited. This review summarizes published reports on streptococcal species, which have been detected in marine mammals. Furthermore, we discuss streptococcal transmission between and adaptation to their marine mammalian hosts. We conclude that streptococci colonize and/or infect marine mammals very frequently, but in many cases, streptococci isolated from marine mammals have not been further identified. How these bacteria disseminate and adapt to their specific niches can only be speculated due to the lack of respective research. Considering the relevance of pathogenic streptococci for marine mammals as part of the marine ecosystem, it seems that they have been neglected and should receive scientific interest in the future.

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27

GRIFFIN, DALE W., ERIN K. LIPP, MOLLY R. McLAUGHLIN, and JOAN B. ROSE. "Marine Recreation and Public Health Microbiology: Quest for the Ideal Indicator." BioScience 51, no. 10 (2001): 817. http://dx.doi.org/10.1641/0006-3568(2001)051[0817:mraphm]2.0.co;2.

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Adler, Antony, and Erik Dücker. "When Pasteurian Science Went to Sea: The Birth of Marine Microbiology." Journal of the History of Biology 51, no. 1 (April 5, 2017): 107–33. http://dx.doi.org/10.1007/s10739-017-9477-8.

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29

Lowe, Chris D., David J. S. Montagnes, Laura E. Martin, and Phillip C. Watts. "Patterns of Genetic Diversity in the Marine Heterotrophic Flagellate Oxyrrhis marina (Alveolata: Dinophyceae)." Protist 161, no. 2 (April 2010): 212–21. http://dx.doi.org/10.1016/j.protis.2009.11.003.

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30

C., Pedrós-Alió, and Simó R. "Studying marine microorganisms from space." International Microbiology 5, no. 4 (December 1, 2002): 195–200. http://dx.doi.org/10.1007/s10123-002-0087-7.

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31

Wemheuer, Bernd. "A Collection of 13 Archaeal and 46 Bacterial Genomes Reconstructed from Marine Metagenomes Derived from the North Sea." Data 5, no. 1 (February 4, 2020): 15. http://dx.doi.org/10.3390/data5010015.

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Marine bacteria are key drivers of ocean biogeochemistry. Despite the increasing number of studies, the complex interaction of marine bacterioplankton communities with their environment is still not fully understood. Additionally, our knowledge about prominent marine lineages is mostly based on genomic information retrieved from single isolates, which do not necessarily represent these groups. Consequently, deciphering the ecological contributions of single bacterioplankton community members is one major challenge in marine microbiology. In the present study, we reconstructed 13 archaeal and 46 bacterial metagenome-assembled genomes (MAGs) from four metagenomic data sets derived from the North Sea. Archaeal MAGs were affiliated to Marine Group II within the Euryarchaeota. Bacterial MAGs mainly belonged to marine groups within the Bacteroidetes as well as alpha- and gammaproteobacteria. In addition, two bacterial MAGs were classified as members of the Actinobacteria and Verrucomicrobiota, respectively. The reconstructed genomes contribute to our understanding of important marine lineages and may serve as a basis for further research on functional traits of these groups.

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Feng, Xiaoyuan, and Peng Xing. "Genomics of Yoonia sp. Isolates (Family Roseobacteraceae) from Lake Zhangnai on the Tibetan Plateau." Microorganisms 11, no. 11 (November 20, 2023): 2817. http://dx.doi.org/10.3390/microorganisms11112817.

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Understanding the genomic differentiation between marine and non-marine aquatic microbes remains a compelling question in ecology. While previous research has identified several lacustrine lineages within the predominantly marine Roseobacteraceae family, limited genomic data have constrained our understanding of their ecological adaptation mechanisms. In this study, we isolated four novel Yoonia strains from a brackish lake on the Tibetan Plateau. These strains have diverged from their marine counterparts within the same genus, indicating a recent habitat transition event from marine to non-marine environments. Metabolic comparisons and ancestral genomic reconstructions in a phylogenetic framework reveal metabolic shifts in salinity adaptation, compound transport, aromatics degradation, DNA repair, and restriction systems. These findings not only corroborate the metabolic changes commonly observed in other non-marine Roseobacters but also unveil unique adaptations, likely reflecting the localized metabolic changes in responses to Tibetan Plateau environments. Collectively, our study expands the known genomic diversity of non-marine Roseobacteraceae lineages and enhances our understanding of microbial adaptations to lacustrine ecosystems.

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Santoro, A. E., M. Kellom, and S. M. Laperriere. "Contributions of single-cell genomics to our understanding of planktonic marine archaea." Philosophical Transactions of the Royal Society B: Biological Sciences 374, no. 1786 (October 7, 2019): 20190096. http://dx.doi.org/10.1098/rstb.2019.0096.

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Single-cell genomics has transformed many fields of biology, marine microbiology included. Here, we consider the impact of single-cell genomics on a specific group of marine microbes—the planktonic marine archaea. Despite single-cell enabled discoveries of novel metabolic function in the marine thaumarchaea, population-level investigations are hindered by an overall lower than expected recovery of thaumarchaea in single-cell studies. Metagenome-assembled genomes have so far been a more useful method for accessing genome-resolved insights into the Marine Group II euryarchaea. Future progress in the application of single-cell genomics to archaeal biology in the ocean would benefit from more targeted sorting approaches, and a more systematic investigation of potential biases against archaea in single-cell workflows including cell lysis, genome amplification and genome screening. This article is part of a discussion meeting issue ‘Single cell ecology’.

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Huo, Ying-Yi, Xue-Wei Xu, Xue Li, Chen Liu, Heng-Lin Cui, Chun-Sheng Wang, and Min Wu. "Ruegeria marina sp. nov., isolated from Marine Sediment." International Journal of Systematic and Evolutionary Microbiology 61, no. 2 (February 1, 2011): 347–50. http://dx.doi.org/10.1099/ijs.0.022400-0.

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A Gram-negative, neutrophilic and rod-shaped bacterium, strain ZH17T, was isolated from a marine sediment of the East China Sea and subjected to a polyphasic taxonomic characterization. The isolate grew in the presence of 0–7.5 % (w/v) NaCl and at pH 6.5–9.0; optimum growth was observed with 0.5–3.0 % (w/v) NaCl and at pH 7.5. Chemotaxonomic analysis showed ubiquinone-10 as predominant respiratory quinone and C18 : 1 ω7c, 11-methyl C18 : 1 ω7c, C16 : 0, C12 : 0 3-OH and C16 : 0 2-OH as major fatty acids. The genomic DNA G+C content was 63.5 mol%. Comparative 16S rRNA gene sequence analysis revealed that the isolate belongs to the genus Ruegeria. Strain ZH17T exhibited the closest phylogenetic affinity to the type strain of Ruegeria pomeroyi, with 97.2 % sequence similarity, and less than 97 % sequence similarity with respect to other described species of the genus Ruegeria. The DNA–DNA reassociation value between strain ZH17T and R. pomeroyi DSM 15171T was 50.7 %. On the basis of phenotypic and genotypic data, strain ZH17T represents a novel species of the genus Ruegeria, for which the name Ruegeria marina sp. nov. (type strain ZH17T =CGMCC 1.9108T =JCM 16262T) is proposed.

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35

Maldonado-Ruiz, Karina, Ruth Pedroza-Islas, and Lorena Pedraza-Segura. "Blue Biotechnology: Marine Bacteria Bioproducts." Microorganisms 12, no. 4 (March 29, 2024): 697. http://dx.doi.org/10.3390/microorganisms12040697.

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The ocean is the habitat of a great number of organisms with different characteristics. Compared to terrestrial microorganisms, marine microorganisms also represent a vast and largely unexplored reservoir of bioactive compounds with diverse industrial applications like terrestrial microorganisms. This review examines the properties and potential applications of products derived from marine microorganisms, including bacteriocins, enzymes, exopolysaccharides, and pigments, juxtaposing them in some cases against their terrestrial counterparts. We discuss the distinct characteristics that set marine-derived products apart, including enhanced stability and unique structural features such as the amount of uronic acid and sulfate groups in exopolysaccharides. Further, we explore the uses of these marine-derived compounds across various industries, ranging from food and pharmaceuticals to cosmetics and biotechnology. This review also presents a broad description of biotechnologically important compounds produced by bacteria isolated from marine environments, some of them with different qualities compared to their terrestrial counterparts.

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36

Hopkinson, Brian M., Kelly L. Roe, and Katherine A. Barbeau. "Heme Uptake by Microscilla marina and Evidence for Heme Uptake Systems in the Genomes of Diverse Marine Bacteria." Applied and Environmental Microbiology 74, no. 20 (August 29, 2008): 6263–70. http://dx.doi.org/10.1128/aem.00964-08.

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ABSTRACT The ability to acquire diverse and abundant forms of iron would be expected to confer a survival advantage in the marine environment, where iron is scarce. Marine bacteria are known to use siderophores and inorganic iron, but their ability to use heme, an abundant intracellular iron form, has only been examined preliminarily. Microscilla marina, a cultured relative of a bacterial group frequently found on marine particulates, was used as a model organism to examine heme uptake. Searches of the genome revealed analogs to known heme transport proteins, and reverse transcription-quantitative PCR analysis of these genes showed that they were expressed and upregulated under iron stress and during growth on heme. M. marina was found to take up heme-bound iron and could grow on heme as a sole iron source, supporting the genetic evidence for heme transport. Similar putative heme transport components were identified in the genomes of diverse marine bacteria. These systems were found in the genomes of many bacteria thought to be particle associated but were lacking in known free-living organisms (e.g., Pelagibacter ubique and marine cyanobacteria). This distribution of transporters is consistent with the hydrophobic, light-sensitive nature of heme, suggesting that it is primarily available on phytoplankton or detritus or in nutrient-rich environments.

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BAKER, J. M., M. W. GRIFFITHS, and D. L. COLLINS-THOMPSON. "Bacterial Bioluminescence: Applications in Food Microbiology." Journal of Food Protection 55, no. 1 (January 1, 1992): 62–70. http://dx.doi.org/10.4315/0362-028x-55.1.62.

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Many marine microorganisms (Vibrio, Photobacterium) are capable of emitting light, that is, they are bioluminescent. The light-yielding reaction is catalyzed by a luciferase, and it involves the oxidation of reduced riboflavin phosphate and a long-chain aldehyde in the presence of oxygen to produce a blue green light. The genes responsible for the luciferase production, (lux A and lux B), aldehyde synthesis (lux C, D, and E), and regulation of luminescence (lux I and lux R) have all been identified, and recent research has resulted in the discovery of three new genes (lux F, G, and H). The ability to genetically engineer dark microorganisms to become light emitting by introducing the lux genes into them has opened up a wide range of applications of bioluminescence. Assays using bacterial bioluminescence for the detection and enumeration of microorganisms are rapid, sensitive, accurate, and can be made specific. It is these attributes that are making in vivo bioluminescent assays so attractive to the food industry.

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Choi, Ahyoung, Kyung-Mi Kim, Ilnam Kang, Seok-Hyun Youn, Young-Sang Suh, Yoon Lee, and Jang-Cheon Cho. "Grimontia marina sp. nov., a marine bacterium isolated from the Yellow Sea." Journal of Microbiology 50, no. 1 (February 2012): 170–74. http://dx.doi.org/10.1007/s12275-012-1615-6.

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39

Dolan, John R. "Marine Protists: Diversity and Dynamics." Journal of Eukaryotic Microbiology 63, no. 3 (March 2, 2016): 410. http://dx.doi.org/10.1111/jeu.12297.

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40

Solanki, Renu, Monisha Khanna, and Rup Lal. "Bioactive compounds from marine actinomycetes." Indian Journal of Microbiology 48, no. 4 (December 2008): 410–31. http://dx.doi.org/10.1007/s12088-008-0052-z.

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41

Hall, Ailsa J. "Morbilliviruses in marine mammals." Trends in Microbiology 3, no. 1 (January 1995): 4–9. http://dx.doi.org/10.1016/s0966-842x(00)88861-7.

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42

Janvier, M., C. Frehel, F. Grimont, and F. Gasser. "Methylophaga marina gen. nov., sp. nov. and Methylophaga thalassica sp. nov., Marine Methylotrophs." International Journal of Systematic Bacteriology 35, no. 2 (April 1, 1985): 131–39. http://dx.doi.org/10.1099/00207713-35-2-131.

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43

Fenchel, Tom. "Marine microbiology: ecology and applications Colin Munn (with foreword by Farooq Azam)." Marine Biology Research 8, no. 1 (January 2012): 100. http://dx.doi.org/10.1080/17451000.2011.626054.

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44

Yamamoto, Haruki, Kazuma Uesaka, Yuki Tsuzuki, Hisanori Yamakawa, Shigeru Itoh, and Yuichi Fujita. "Comparative Genomic Analysis of the Marine Cyanobacterium Acaryochloris marina MBIC10699 Reveals the Impact of Phycobiliprotein Reacquisition and the Diversity of Acaryochloris Plasmids." Microorganisms 10, no. 7 (July 7, 2022): 1374. http://dx.doi.org/10.3390/microorganisms10071374.

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Acaryochloris is a marine cyanobacterium that synthesizes chlorophyll d, a unique chlorophyll that absorbs far-red lights. Acaryochloris is also characterized by the loss of phycobiliprotein (PBP), a photosynthetic antenna specific to cyanobacteria; however, only the type-strain A. marina MBIC11017 retains PBP, suggesting that PBP-related genes were reacquired through horizontal gene transfer (HGT). Acaryochloris is thought to have adapted to various environments through its huge genome size and the genes acquired through HGT; however, genomic information on Acaryochloris is limited. In this study, we report the complete genome sequence of A. marina MBIC10699, which was isolated from the same area of ocean as A. marina MBIC11017 as a PBP-less strain. The genome of A. marina MBIC10699 consists of a 6.4 Mb chromosome and four large plasmids totaling about 7.6 Mb, and the phylogenic analysis shows that A. marina MBIC10699 is the most closely related to A. marina MBIC11017 among the Acaryochloris species reported so far. Compared with A. marina MBIC11017, the chromosomal genes are highly conserved between them, while the genes encoded in the plasmids are significantly diverse. Comparing these genomes provides clues as to how the genes for PBPs were reacquired and what changes occurred in the genes for photosystems during evolution.

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Cecchi, Grazia, Laura Cutroneo, Simone Di Piazza, Giovanni Besio, Marco Capello, and Mirca Zotti. "Port Sediments: Problem or Resource? A Review Concerning the Treatment and Decontamination of Port Sediments by Fungi and Bacteria." Microorganisms 9, no. 6 (June 11, 2021): 1279. http://dx.doi.org/10.3390/microorganisms9061279.

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Contamination of marine sediments by organic and/or inorganic compounds represents one of the most critical problems in marine environments. This issue affects not only biodiversity but also ecosystems, with negative impacts on sea water quality. The scientific community and the European Commission have recently discussed marine environment and ecosystem protection and restoration by sustainable green technologies among the main objectives of their scientific programmes. One of the primary goals of sustainable restoration and remediation of contaminated marine sediments is research regarding new biotechnologies employable in the decontamination of marine sediments, to consider sediments as a resource in many fields such as industry. In this context, microorganisms—in particular, fungi and bacteria—play a central and crucial role as the best tools of sustainable and green remediation processes. This review, carried out in the framework of the Interreg IT-FR Maritime GEREMIA Project, collects and shows the bioremediation and mycoremediation studies carried out on marine sediments contaminated with ecotoxic metals and organic pollutants. This work evidences the potentialities and limiting factors of these biotechnologies and outlines the possible future scenarios of the bioremediation of marine sediments, and also highlights the opportunities of an integrated approach that involves fungi and bacteria together.

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Levine, Naomi M., and Suzana G. Leles. "Marine plankton metabolisms revealed." Nature Microbiology 6, no. 2 (January 28, 2021): 147–48. http://dx.doi.org/10.1038/s41564-020-00856-x.

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de Oliveira, Bruno Francesco Rodrigues, and Yahyah Yusuff. "Culturing enigmatic marine bacteria." Nature Microbiology 9, no. 1 (January 4, 2024): 6–7. http://dx.doi.org/10.1038/s41564-023-01567-9.

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Dann, Lisa M., Stephanie Rosales, Jody McKerral, James S. Paterson, Renee J. Smith, Thomas C. Jeffries, Rod L. Oliver, and James G. Mitchell. "Marine and giant viruses as indicators of a marine microbial community in a riverine system." MicrobiologyOpen 5, no. 6 (August 9, 2016): 1071–84. http://dx.doi.org/10.1002/mbo3.392.

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Liu, Pan, Haiting Zhang, Yongqiang Fan, and Dake Xu. "Microbially Influenced Corrosion of Steel in Marine Environments: A Review from Mechanisms to Prevention." Microorganisms 11, no. 9 (September 12, 2023): 2299. http://dx.doi.org/10.3390/microorganisms11092299.

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Microbially influenced corrosion (MIC) is a formidable challenge in the marine industry, resulting from intricate interactions among various biochemical reactions and microbial species. Many preventions used to mitigate biocorrosion fail due to ignorance of the MIC mechanisms. This review provides a summary of the current research on microbial corrosion in marine environments, including corrosive microbes and biocorrosion mechanisms. We also summarized current strategies for inhibiting MIC and proposed future research directions for MIC mechanisms and prevention. This review aims to comprehensively understand marine microbial corrosion and contribute to novel strategy developments for biocorrosion control in marine environments.

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Kueh, C. S. W., P. Kutarski, and M. Brunton. "Contaminated marine wounds-the risk of acquiring acute bacterial infection from marine recreational beaches." Journal of Applied Bacteriology 73, no. 5 (November 1992): 412–20. http://dx.doi.org/10.1111/j.1365-2672.1992.tb04997.x.

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Journal articles on the topic 'Marine microbiology'

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