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Journal articles on the topic 'Aerobic anoxygenic phototrophic bacteria'

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Published: 2 June 2025

Last updated: 31 July 2025

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1

Eiler, Alexander, Sara Beier, Christin Sï¿½wstrï¿½m, Jan Karlsson, and Stefan Bertilsson. "High Ratio of Bacteriochlorophyll Biosynthesis Genes to Chlorophyll Biosynthesis Genes in Bacteria of Humic Lakes." Applied and Environmental Microbiology 75, no. 22 (2009): 7221–28. http://dx.doi.org/10.1128/aem.00960-09.

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ABSTRACT Recent studies highlight the diversity and significance of marine phototrophic microorganisms such as picocyanobacteria, phototrophic picoeukaryotes, and bacteriochlorophyll- and rhodopsin-holding phototrophic bacteria. To assess if freshwater ecosystems also harbor similar phototroph diversity, genes involved in the biosynthesis of bacteriochlorophyll and chlorophyll were targeted to explore oxygenic and aerobic anoxygenic phototroph composition in a wide range of lakes. Partial dark-operative protochlorophyllide oxidoreductase (DPOR) and chlorophyllide oxidoreductase (COR) genes in

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2

Yurkov, Vladimir V., and J. Thomas Beatty. "Aerobic Anoxygenic Phototrophic Bacteria." Microbiology and Molecular Biology Reviews 62, no. 3 (1998): 695–724. http://dx.doi.org/10.1128/mmbr.62.3.695-724.1998.

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SUMMARY The aerobic anoxygenic phototrophic bacteria are a relatively recently discovered bacterial group. Although taxonomically and phylogenetically heterogeneous, these bacteria share the following distinguishing features: the presence of bacteriochlorophyll a incorporated into reaction center and light-harvesting complexes, low levels of the photosynthetic unit in cells, an abundance of carotenoids, a strong inhibition by light of bacteriochlorophyll synthesis, and the inability to grow photosynthetically under anaerobic conditions. Aerobic anoxygenic phototrophic bacteria are classified i

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3

Messner, Katia, and Vladimir Yurkov. "Abundance, Characterization and Diversity of Culturable Anoxygenic Phototrophic Bacteria in Manitoban Marshlands." Microorganisms 12, no. 5 (2024): 1007. http://dx.doi.org/10.3390/microorganisms12051007.

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Marshes are an important ecosystem, acting as a biodiversity hotspot, a carbon sink and a bioremediation site, breaking down anthropogenic waste such as antibiotics, metals and fertilizers. Due to their participation in these metabolic activities and their capability to contribute to primary productivity, the microorganisms in such habitats have become of interest to investigate. Since Proteobacteria were previously found to be abundant and the waters are well aerated and organic-rich, this study on the presence of anoxygenic phototrophic bacteria, purple non-sulfur bacteria and aerobic anoxyg

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4

Imhoff, Johannes F., Tanja Rahn, Sven Künzel, and Sven C. Neulinger. "Phylogeny of Anoxygenic Photosynthesis Based on Sequences of Photosynthetic Reaction Center Proteins and a Key Enzyme in Bacteriochlorophyll Biosynthesis, the Chlorophyllide Reductase." Microorganisms 7, no. 11 (2019): 576. http://dx.doi.org/10.3390/microorganisms7110576.

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Photosynthesis is a key process for the establishment and maintenance of life on earth, and it is manifested in several major lineages of the prokaryote tree of life. The evolution of photosynthesis in anoxygenic photosynthetic bacteria is of major interest as these have the most ancient roots of photosynthetic systems. The phylogenetic relations between anoxygenic phototrophic bacteria were compared on the basis of sequences of key proteins of the type-II photosynthetic reaction center, including PufLM and PufH (PuhA), and a key enzyme of bacteriochlorophyll biosynthesis, the light-independen

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5

ZHANG, Yao. "Method for quantification of aerobic anoxygenic phototrophic bacteria." Chinese Science Bulletin 49, no. 6 (2004): 597. http://dx.doi.org/10.1360/03wc0447.

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6

Cottrell, Matthew T., Antonio Mannino, and David L. Kirchman. "Aerobic Anoxygenic Phototrophic Bacteria in the Mid-Atlantic Bight and the North Pacific Gyre." Applied and Environmental Microbiology 72, no. 1 (2006): 557–64. http://dx.doi.org/10.1128/aem.72.1.557-564.2006.

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ABSTRACT The abundance of aerobic anoxygenic phototrophic (AAP) bacteria, cyanobacteria, and heterotrophs was examined in the Mid-Atlantic Bight and the central North Pacific Gyre using infrared fluorescence microscopy coupled with image analysis and flow cytometry. AAP bacteria comprised 5% to 16% of total prokaryotes in the Atlantic Ocean but only 5% or less in the Pacific Ocean. In the Atlantic, AAP bacterial abundance was as much as 2-fold higher than that of Prochlorococcus spp. and 10-fold higher than that of Synechococcus spp. In contrast, Prochlorococcus spp. outnumbered AAP bacteria 5

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7

Lamy, D., C. Jeanthon, J. Ras, et al. "Ecology of aerobic anoxygenic phototrophic bacteria along an oligotrophic gradient in the Mediterranean Sea." Biogeosciences Discussions 8, no. 1 (2011): 323–54. http://dx.doi.org/10.5194/bgd-8-323-2011.

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Abstract. Aerobic anoxygenic phototrophic (AAP) bacteria are photoheterotrophic prokaryotes able to use both light and organic substrates for energy production. They are widely distributed in coastal and oceanic environments and may contribute significantly to the carbon cycle in the upper ocean. To better understand questions regarding links between the ecology of these photoheterotrophic bacteria and the trophic status of water masses, we examined their horizontal and vertical distribution and the effects of nutrient additions on their growth along an oligotrophic gradient in the Mediterrane

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8

Lamy, D., C. Jeanthon, M. T. Cottrell, et al. "Ecology of aerobic anoxygenic phototrophic bacteria along an oligotrophic gradient in the Mediterranean Sea." Biogeosciences 8, no. 4 (2011): 973–85. http://dx.doi.org/10.5194/bg-8-973-2011.

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Abstract. Aerobic anoxygenic phototrophic (AAP) bacteria are photoheterotrophic prokaryotes able to use both light and organic substrates for energy production. They are widely distributed in coastal and oceanic environments and may contribute significantly to the carbon cycle in the upper ocean. To better understand questions regarding links between the ecology of these photoheterotrophic bacteria and the trophic status of water masses, we examined their horizontal and vertical distribution and the effects of nutrient additions on their growth along an oligotrophic gradient in the Mediterrane

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9

Yutin, Natalya, Marcelino T. Suzuki, and Oded Béjà. "Novel Primers Reveal Wider Diversity among Marine Aerobic Anoxygenic Phototrophs." Applied and Environmental Microbiology 71, no. 12 (2005): 8958–62. http://dx.doi.org/10.1128/aem.71.12.8958-8962.2005.

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ABSTRACT Aerobic anoxygenic phototrophic bacteria (AAnPs) were previously proposed to account for up to 11% of marine bacterioplankton and to potentially have great ecological importance in the world's oceans. Our data show that previously used primers based on the M subunit of anoxygenic photosynthetic reaction center genes (pufM) do not comprehensively identify the diversity of AAnPs in the ocean. We have designed and tested a new set of pufM-specific primers and revealed several new AAnP variants in environmental DNA samples and genomic libraries.

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10

Zhang, Yongyu, та Nianzhi Jiao. "Roseophage RDJLΦ1, Infecting the Aerobic Anoxygenic Phototrophic Bacterium Roseobacter denitrificans OCh114". Applied and Environmental Microbiology 75, № 6 (2009): 1745–49. http://dx.doi.org/10.1128/aem.02131-08.

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ABSTRACT A marine roseophage RDJLΦ1 lytically infecting Roseobacter denitrificans OCh114 was isolated and characterized. RDJLΦ1 can package several host cellular proteins into its virions, and its DNA is refractory to several commonly used restriction enzymes. This paper presents the first report of a bacteriophage isolated from the aerobic anoxygenic phototrophic bacteria.

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11

Ruivo, Mickael, Paulo Cartaxana, Maria Inês Cardoso, Ana Tenreiro, Rogério Tenreiro, and Bruno Jesus. "Extraction and quantification of pigments in aerobic anoxygenic phototrophic bacteria." Limnology and Oceanography: Methods 12, no. 6 (2014): 338–50. http://dx.doi.org/10.4319/lom.2014.12.338.

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12

Koh, Eileen Y., William Phua, and Ken G. Ryan. "Aerobic anoxygenic phototrophic bacteria in Antarctic sea ice and seawater." Environmental Microbiology Reports 3, no. 6 (2011): 710–16. http://dx.doi.org/10.1111/j.1758-2229.2011.00286.x.

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13

JIAO, Nianzhi. "Aerobic anoxygenic phototrophic bacteria and their roles in marine ecosystems." Chinese Science Bulletin 48, no. 11 (2003): 1064. http://dx.doi.org/10.1360/02wc0336.

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14

Jiao, Nianzhi, Michael E. Sieracki, Yao Zhang, and Hailian Du. "Aerobic anoxygenic phototrophic bacteria and their roles in marine ecosystems." Chinese Science Bulletin 48, no. 11 (2003): 1064–68. http://dx.doi.org/10.1007/bf03185754.

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15

Sato-Takabe, Yuki, Setsuko Hirose, Tomoyuki Hori, and Satoshi Hanada. "Abundance and Spatial Distribution of Aerobic Anoxygenic Phototrophic Bacteria in Tama River, Japan." Water 12, no. 1 (2020): 150. http://dx.doi.org/10.3390/w12010150.

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Aerobic anoxygenic phototrophic bacteria (AAnPB) are widely distributed and regarded as key players driving the carbon cycle in surface water of global oceans, coastal and estuary areas and in other freshwater environments (e.g., ponds and lakes). However, the abundance and spatial distribution of AAnPB in rivers is much less well-known. Here we investigated the variation of the absolute cell abundances of the total bacteria, AAnPB and cyanobacteria, at four different sites in Tama River, Japan, and the spatial distribution (i.e., free-living or particle-attached existence form) of AAnPB at tw

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16

Stegman, Monica R., Matthew T. Cottrell, and David L. Kirchman. "Leucine incorporation by aerobic anoxygenic phototrophic bacteria in the Delaware estuary." ISME Journal 8, no. 11 (2014): 2339–48. http://dx.doi.org/10.1038/ismej.2014.75.

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17

Zhang, Yao, and Nianzhi Jiao. "Dynamics of aerobic anoxygenic phototrophic bacteria in the East China Sea." FEMS Microbiology Ecology 61, no. 3 (2007): 459–69. http://dx.doi.org/10.1111/j.1574-6941.2007.00355.x.

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18

Csotonyi, Julius T., Jolantha Swiderski, Erko Stackebrandt, and Vladimir Yurkov. "A new environment for aerobic anoxygenic phototrophic bacteria: biological soil crusts." Environmental Microbiology Reports 2, no. 5 (2010): 651–56. http://dx.doi.org/10.1111/j.1758-2229.2010.00151.x.

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19

Zheng, Qiang, Rui Zhang, Michal Koblížek, et al. "Diverse Arrangement of Photosynthetic Gene Clusters in Aerobic Anoxygenic Phototrophic Bacteria." PLoS ONE 6, no. 9 (2011): e25050. http://dx.doi.org/10.1371/journal.pone.0025050.

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20

Sato‐Takabe, Yuki, Koji Hamasaki, and Satoru Suzuki. "High temperature accelerates growth of aerobic anoxygenic phototrophic bacteria in seawater." MicrobiologyOpen 8, no. 5 (2018): e00710. http://dx.doi.org/10.1002/mbo3.710.

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21

Boeuf, Dominique, Matthew T. Cottrell, David L. Kirchman, et al. "Summer community structure of aerobic anoxygenic phototrophic bacteria in the western Arctic Ocean." FEMS microbiology ecology 85, no. 3 (2013): 1–16. https://doi.org/10.1111/1574-6941.12130.

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Aerobic anoxygenic phototrophic (AAP) bacteria are found in a range of aquatic and terrestrial environments, potentially playing unique roles in biogeochemical cycles. Although known to occur in the Arctic Ocean, their ecology and the factors that govern their community structure and distribution in this extreme environment are poorly understood. Here, we examined summer AAP abundance and diversity in the North East Pacific and the Arctic Ocean with emphasis on the southern Beaufort Sea. AAP bacteria comprised up to 10 and 14% of the prokaryotic community in the bottom nepheloid layer and surf

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22

Lami, Raphaël, Matthew T. Cottrell, Joséphine Ras, et al. "High Abundances of Aerobic Anoxygenic Photosynthetic Bacteria in the South Pacific Ocean." Applied and Environmental Microbiology 73, no. 13 (2007): 4198–205. http://dx.doi.org/10.1128/aem.02652-06.

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ABSTRACT Little is known about the abundance, distribution, and ecology of aerobic anoxygenic phototrophic (AAP) bacteria, particularly in oligotrophic environments, which represent 60% of the ocean. We investigated the abundance of AAP bacteria across the South Pacific Ocean, including the center of the gyre, the most oligotrophic water body of the world ocean. AAP bacteria, Prochlorococcus, and total prokaryotic abundances, as well as bacteriochlorophyll a (BChl a) and divinyl-chlorophyll a concentrations, were measured at several depths in the photic zone along a gradient of oligotrophic co

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23

Bachar, Ami, Enoma Omoregie, Rutger de Wit, and Henk M. Jonkers. "Diversity and Function of Chloroflexus-Like Bacteria in a Hypersaline Microbial Mat: Phylogenetic Characterization and Impact on Aerobic Respiration." Applied and Environmental Microbiology 73, no. 12 (2007): 3975–83. http://dx.doi.org/10.1128/aem.02532-06.

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ABSTRACT We studied the diversity of Chloroflexus-like bacteria (CLB) in a hypersaline phototrophic microbial mat and assayed their near-infrared (NIR) light-dependent oxygen respiration rates. PCR with primers that were reported to specifically target the 16S rRNA gene from members of the phylum Chloroflexi resulted in the recovery of 49 sequences and 16 phylotypes (sequences of the same phylotype share more than 96% similarity), and 10 of the sequences (four phylotypes) appeared to be related to filamentous anoxygenic phototrophic members of the family Chloroflexaceae. Photopigment analysis

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24

Hauruseu, Dzmitry, and Michal Koblížek. "Influence of Light on Carbon Utilization in Aerobic Anoxygenic Phototrophs." Applied and Environmental Microbiology 78, no. 20 (2012): 7414–19. http://dx.doi.org/10.1128/aem.01747-12.

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ABSTRACTAerobic anoxygenic phototrophs contain photosynthetic reaction centers composed of bacteriochlorophyll. These organisms are photoheterotrophs, as they require organic carbon substrates for their growth whereas light-derived energy has only an auxiliary function. To establish the contribution of light energy to their metabolism, we grew the phototrophic strainErythrobactersp. NAP1 in a carbon-limited chemostat regimen on defined carbon sources (glutamate, pyruvate, acetate, and glucose) under conditions of different light intensities. When grown in a light-dark cycle, these bacteria acc

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25

Mašín, M., Z. Čuperová, E. Hojerová, I. Salka, HP Grossart, and M. Koblížek. "Distribution of aerobic anoxygenic phototrophic bacteria in glacial lakes of northern Europe." Aquatic Microbial Ecology 66, no. 1 (2012): 77–86. http://dx.doi.org/10.3354/ame01558.

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26

Sato-Takabe, Yuki, Koji Hamasaki, and Koji Suzuki. "Photosynthetic characteristics of marine aerobic anoxygenic phototrophic bacteria Roseobacter and Erythrobacter strains." Archives of Microbiology 194, no. 5 (2011): 331–41. http://dx.doi.org/10.1007/s00203-011-0761-2.

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27

Waidner, Lisa A., and David L. Kirchman. "Aerobic Anoxygenic Phototrophic Bacteria Attached to Particles in Turbid Waters of the Delaware and Chesapeake Estuaries." Applied and Environmental Microbiology 73, no. 12 (2007): 3936–44. http://dx.doi.org/10.1128/aem.00592-07.

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ABSTRACT Aerobic anoxygenic phototrophic (AAP) bacteria are photoheterotrophs that, if abundant, may be biogeochemically important in the oceans. We used epifluorescence microscopy and quantitative PCR (qPCR) to examine the abundance of these bacteria by enumerating cells with bacteriochlorophyll a (bChl a) and the light-reaction center gene pufM, respectively. In the surface waters of the Delaware estuary, AAP bacteria were abundant, comprising up to 34% of prokaryotes, although the percentage varied greatly with location and season. On average, AAP bacteria made up 12% of the community as me

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Ritchie, Anna E., and Zackary I. Johnson. "Abundance and Genetic Diversity of Aerobic Anoxygenic Phototrophic Bacteria of Coastal Regions of the Pacific Ocean." Applied and Environmental Microbiology 78, no. 8 (2012): 2858–66. http://dx.doi.org/10.1128/aem.06268-11.

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ABSTRACTAerobic anoxygenic phototrophic (AAP) bacteria are photoheterotrophic microbes that are found in a broad range of aquatic environments. Although potentially significant to the microbial ecology and biogeochemistry of marine ecosystems, their abundance and genetic diversity and the environmental variables that regulate these properties are poorly understood. Using samples along nearshore/offshore transects from five disparate islands in the Pacific Ocean (Oahu, Molokai, Futuna, Aniwa, and Lord Howe) and off California, we show that AAP bacteria, as quantified by thepufMgene biomarker, a

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Boldareva-Nuianzina, Ekaterina N., Zuzana Bláhová, Roman Sobotka, and Michal Koblížek. "Distribution and Origin of Oxygen-Dependent and Oxygen-Independent Forms of Mg-Protoporphyrin Monomethylester Cyclase among Phototrophic Proteobacteria." Applied and Environmental Microbiology 79, no. 8 (2013): 2596–604. http://dx.doi.org/10.1128/aem.00104-13.

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ABSTRACTMagnesium-protoporphyrin IX monomethylester cyclase is one of the key enzymes of the bacteriochlorophyll biosynthesis pathway. There exist two fundamentally different forms of this enzyme. The oxygen-dependent form, encoded by the geneacsF, catalyzes the formation of the bacteriochlorophyll fifth ring using oxygen, whereas the oxygen-independent form encoded by the genebchEutilizes an oxygen atom extracted from water. The presence ofacsFandbchEgenes was surveyed in various phototrophicProteobacteriausing the available genomic data and newly designed degenerated primers. It was found th

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Ferrera, Isabel, Olga Sánchez, Eva Kolářová, Michal Koblížek, and Josep M. Gasol. "Light enhances the growth rates of natural populations of aerobic anoxygenic phototrophic bacteria." ISME Journal 11, no. 10 (2017): 2391–93. http://dx.doi.org/10.1038/ismej.2017.79.

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31

Rontani, J. F., S. Christodoulou, and M. Koblizek. "GC-MS structural characterization of fatty acids from marine aerobic anoxygenic phototrophic bacteria." Lipids 40, no. 1 (2005): 97–108. http://dx.doi.org/10.1007/s11745-005-1364-6.

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32

Boeuf, Dominique, Matthew T. Cottrell, David L. Kirchman, Philippe Lebaron, and Christian Jeanthon. "Summer community structure of aerobic anoxygenic phototrophic bacteria in the western Arctic Ocean." FEMS Microbiology Ecology 85, no. 3 (2013): 417–32. http://dx.doi.org/10.1111/1574-6941.12130.

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33

Davenport, Emily J., and Arpita Bose. "Taxonomic Re-Evaluation and Genomic Comparison of Novel Extracellular Electron Uptake-Capable Rhodovulum visakhapatnamense and Rhodovulum sulfidophilum Isolates." Microorganisms 10, no. 6 (2022): 1235. http://dx.doi.org/10.3390/microorganisms10061235.

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Rhodovulum spp. are anoxygenic phototrophic purple bacteria with versatile metabolisms, including the ability to obtain electrons from minerals in their environment to drive photosynthesis, a relatively novel process called phototrophic extracellular electron uptake (pEEU). A total of 15 strains of Rhodovulum sulfidophilum were isolated from a marine estuary to observe these metabolisms in marine phototrophs. One representative strain, Rhodovulum sulfidophilum strain AB26, can perform phototrophic iron oxidation (photoferrotrophy) and couples carbon dioxide fixation to pEEU. Here, we reclassif

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Ferrera, Isabel, Josep M. Gasol, Marta Sebastián, Eva Hojerová, and Michal Koblížek. "Comparison of Growth Rates of Aerobic Anoxygenic Phototrophic Bacteria and Other Bacterioplankton Groups in Coastal Mediterranean Waters." Applied and Environmental Microbiology 77, no. 21 (2011): 7451–58. http://dx.doi.org/10.1128/aem.00208-11.

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ABSTRACTGrowth is one of the basic attributes of any living organism. Surprisingly, the growth rates of marine bacterioplankton are only poorly known. Current data suggest that marine bacteria grow relatively slowly, having generation times of several days. However, some bacterial groups, such as the aerobic anoxygenic phototrophic (AAP) bacteria, have been shown to grow much faster. Two manipulation experiments, in which grazing, viruses, and resource competition were reduced, were conducted in the coastal Mediterranean Sea (Blanes Bay Microbial Observatory). The growth rates of AAP bacteria

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35

Ye, Yu-Qi, Ji-Ru Han, Jin-Xin Zhao, Meng-Qi Ye, and Zong-Jun Du. "Genomic Analysis and Characterization of Pseudotabrizicola formosa sp. nov., a Novel Aerobic Anoxygenic Phototrophic Bacterium, Isolated from Sayram Lake Water." Microorganisms 10, no. 11 (2022): 2154. http://dx.doi.org/10.3390/microorganisms10112154.

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Aerobic anoxygenic photosynthetic bacteria (AAPB) are a kind of heterotrophic prokaryote that can use bacteriochlorophyll (BChl) for photosynthesis without oxygen production and they are widely distributed in aquatic environments, including oceans, lakes, and rivers. A novel aerobic anoxygenic photosynthetic bacterium strain XJSPT was isolated during a study of water microbial diversity in Sayram Lake, Xinjiang Province, China. Strain XJSPT was found to grow optimally at 33 °C, pH 7.5 with 1.0% (w/v) NaCl, and to produce bacteriochlorophyll a and carotenoids. Phylogenetic analysis based on 16S

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Kopejtka, Karel, Yonghui Zeng, David Kaftan, et al. "Characterization of the Aerobic Anoxygenic Phototrophic Bacterium Sphingomonas sp. AAP5." Microorganisms 9, no. 4 (2021): 768. http://dx.doi.org/10.3390/microorganisms9040768.

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An aerobic, yellow-pigmented, bacteriochlorophyll a-producing strain, designated AAP5 (=DSM 111157=CCUG 74776), was isolated from the alpine lake Gossenköllesee located in the Tyrolean Alps, Austria. Here, we report its description and polyphasic characterization. Phylogenetic analysis of the 16S rRNA gene showed that strain AAP5 belongs to the bacterial genus Sphingomonas and has the highest pairwise 16S rRNA gene sequence similarity with Sphingomonas glacialis (98.3%), Sphingomonas psychrolutea (96.8%), and Sphingomonas melonis (96.5%). Its genomic DNA G + C content is 65.9%. Further, in sil

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Lami, R., Z. âuperová, J. Ras, P. Lebaron, and M. KoblíÏek. "Distribution of free-living and particle-attached aerobic anoxygenic phototrophic bacteria in marine environments." Aquatic Microbial Ecology 55 (March 18, 2009): 31–38. http://dx.doi.org/10.3354/ame01282.

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38

Sato-Takabe, Yuki. "A highly eff ective survival strategy of aerobic anoxygenic phototrophic bacteria in the ocean." Oceanography in Japan 29, no. 6 (2020): 189–216. http://dx.doi.org/10.5928/kaiyou.29.6_189.

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39

Cottrell, Matthew T., Josephine Ras, and David L. Kirchman. "Bacteriochlorophyll and community structure of aerobic anoxygenic phototrophic bacteria in a particle-rich estuary." ISME Journal 4, no. 7 (2010): 945–54. http://dx.doi.org/10.1038/ismej.2010.13.

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40

Chen, Yao, Yao Zhang, and Nianzhi Jiao. "Responses of aerobic anoxygenic phototrophic bacteria to algal blooms in the East China Sea." Hydrobiologia 661, no. 1 (2010): 435–43. http://dx.doi.org/10.1007/s10750-010-0553-8.

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41

Hirose, Setsuko, Katsumi Matsuura, and Shin Haruta. "Phylogenetically Diverse Aerobic Anoxygenic Phototrophic Bacteria Isolated from Epilithic Biofilms in Tama River, Japan." Microbes and Environments 31, no. 3 (2016): 299–306. http://dx.doi.org/10.1264/jsme2.me15209.

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42

Sato-Takabe, Yuki, Koji Hamasaki, and Koji Suzuki. "Erratum to: Photosynthetic characteristics of marine aerobic anoxygenic phototrophic bacteria Roseobacter and Erythrobacter strains." Archives of Microbiology 194, no. 5 (2011): 343. http://dx.doi.org/10.1007/s00203-011-0772-z.

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43

Gorlenko, V. M., and M. B. Vainshtein. "Microbiological Characteristics of Three Stratified Lakes in the Nizhny Novgorod Region." Микробиология 92, no. 2 (2023): 160–70. http://dx.doi.org/10.31857/s0026365622600699.

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Abstract—Three karst lakes were investigated in the Nizhny Novgorod region: Staropustynskie lakes Svyato and Nekrasov Bay and Lake Svetloyar. The studied lakes belonged to the mesotrophic-eutrophic polyhumous type and were characterized by stable stratification with signs of meromixia. Their water columns were divided into aerobic and anaerobic zones, with the bottom water containing sulfide. Fe(II) compounds were also present in the Staropustynskie lakes. In the Lake Nekrasov Bay, the mixolimnion showed a high rate of oxygenic photosynthesis, up to 1.2 µg С L–1 day–1, as well as a maximum of

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44

Aprilyanto, Victor, Tjut Sugandawaty Djohan, and Langkah Sembiring. "DISTRIBUTION AND ABUNDANCE OF AEROBIC ANOXYGENIC PHOTOTROPHIC BACTERIA IN THE TROPICAL COASTAL WATERS OF GUNUNGKIDUL, YOGYAKARTA." KnE Life Sciences 2, no. 1 (2015): 244. http://dx.doi.org/10.18502/kls.v2i1.150.

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<p>This research was conducted to reveal the distribution and abundance of aerobic anoxygenic phototrophic (AAP) in the tropical coastal waters of Gunungkidul, Yogyakarta. Sampling site was determined at the coastal fish catchment area. We sampled and enumerated total bacterioplankton and AAP bacteria at four sampling depth which are 0, 4, 6, and 20 metre with five replicates each. Several dissolved nutrients such as nitrate, ammonium, phosphate, and sulfate in each respective depths were also measured. Several fluctuations in the nutrient distributions were observed and hypothesized as

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45

Jeanthon, C., D. Boeuf, O. Dahan, et al. "Diversity of cultivated and metabolically active aerobic anoxygenic phototrophic bacteria along an oligotrophic gradient in the Mediterranean Sea." Biogeosciences Discussions 8, no. 3 (2011): 4421–57. http://dx.doi.org/10.5194/bgd-8-4421-2011.

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Abstract. Aerobic anoxygenic phototrophic (AAP) bacteria play significant roles in the bacterioplankton productivity and biogeochemical cycles of the surface ocean. In this study, we applied both cultivation and mRNA-based molecular methods to explore the diversity of AAP bacteria along an oligotrophic gradient in the Mediterranean Sea in early summer 2008. Colony-forming units obtained on three different agar media were screened for the production of bacteriochlorophyll-a (BChl-a), the light-harvesting pigment of AAP bacteria. BChl-a-containing colonies represented a low part of the cultivabl

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Jeanthon, C., D. Boeuf, O. Dahan, et al. "Diversity of cultivated and metabolically active aerobic anoxygenic phototrophic bacteria along an oligotrophic gradient in the Mediterranean Sea." Biogeosciences 8, no. 7 (2011): 1955–70. http://dx.doi.org/10.5194/bg-8-1955-2011.

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Abstract:

Abstract. Aerobic anoxygenic phototrophic (AAP) bacteria play significant roles in the bacterioplankton productivity and biogeochemical cycles of the surface ocean. In this study, we applied both cultivation and mRNA-based molecular methods to explore the diversity of AAP bacteria along an oligotrophic gradient in the Mediterranean Sea in early summer 2008. Colony-forming units obtained on three different agar media were screened for the production of bacteriochlorophyll-a (BChl-a), the light-harvesting pigment of AAP bacteria. BChl-a-containing colonies represented a low part of the cultivabl

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Jiang, Hongchen, Hailiang Dong, Bingsong Yu, et al. "Abundance and diversity of aerobic anoxygenic phototrophic bacteria in saline lakes on the Tibetan plateau." FEMS Microbiology Ecology 67, no. 2 (2009): 268–78. http://dx.doi.org/10.1111/j.1574-6941.2008.00616.x.

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Garcia-Chaves, Maria C., Matthew T. Cottrell, David L. Kirchman, Clara Ruiz-González, and Paul A. del Giorgio. "Single-cell activity of freshwater aerobic anoxygenic phototrophic bacteria and their contribution to biomass production." ISME Journal 10, no. 7 (2016): 1579–88. http://dx.doi.org/10.1038/ismej.2015.242.

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Sato-Takabe, Yuki, Shotaro Suzuki, Ryuki Shishikura, et al. "Spatial distribution and cell size of aerobic anoxygenic phototrophic bacteria in the Uwa Sea, Japan." Journal of Oceanography 71, no. 1 (2014): 151–59. http://dx.doi.org/10.1007/s10872-014-0267-z.

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Gribben, Deborah L., Gavin N. Rees, and Roger L. Croome. "Anoxygenic phototrophic bacteria and aerobic phototrophs in Normans Lagoon, a ‘billabong’ adjacent to the Murray River, south-eastern Australia." Lakes & Reservoirs: Research & Management 8, no. 2 (2003): 95–104. http://dx.doi.org/10.1046/j.1320-5331.2003.00219.x.

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