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1

Knaff, David B. "Anoxygenic photosynthetic bacteria." Photosynthesis Research 47, no. 2 (1996): 199–200. http://dx.doi.org/10.1007/bf00016182.

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2

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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3

Ritchie, Raymond J., Anthony W. D. Larkum, and Ignasi Ribas. "Could photosynthesis function on Proxima Centauri b?" International Journal of Astrobiology 17, no. 2 (2017): 147–76. http://dx.doi.org/10.1017/s1473550417000167.

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AbstractCould oxygenic and/or anoxygenic photosynthesis exist on planet Proxima Centauri b? Proxima Centauri (spectral type – M5.5 V, 3050 K) is a red dwarf, whereas the Sun is type G2 V (5780 K). The light regimes on Earth and Proxima Centauri b are compared with estimates of the planet's suitability for Chlorophylla(Chla) and Chld-based oxygenic photosynthesis and for bacteriochlorophyll (BChl)-based anoxygenic photosynthesis. Proxima Centauri b has low irradiance in the oxygenic photosynthesis range (400–749 nm: 64–132 µmol quanta m−2s−1). Much larger amounts of light would be available for
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4

Klatt, Judith M., Mohammad A. A. Al-Najjar, Pelin Yilmaz, Gaute Lavik, Dirk de Beer, and Lubos Polerecky. "Anoxygenic Photosynthesis Controls Oxygenic Photosynthesis in a Cyanobacterium from a Sulfidic Spring." Applied and Environmental Microbiology 81, no. 6 (2015): 2025–31. http://dx.doi.org/10.1128/aem.03579-14.

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ABSTRACTBefore the Earth's complete oxygenation (0.58 to 0.55 billion years [Ga] ago), the photic zone of the Proterozoic oceans was probably redox stratified, with a slightly aerobic, nutrient-limited upper layer above a light-limited layer that tended toward euxinia. In such oceans, cyanobacteria capable of both oxygenic and sulfide-driven anoxygenic photosynthesis played a fundamental role in the global carbon, oxygen, and sulfur cycle. We have isolated a cyanobacterium,Pseudanabaenastrain FS39, in which this versatility is still conserved, and we show that the transition between the two ph
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5

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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6

Eiler, Alexander, Sara Beier, Christin S�wstr�m, 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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7

Oh, Hyun-Myung, Stephen J. Giovannoni, Steve Ferriera, Justin Johnson, and Jang-Cheon Cho. "Complete Genome Sequence of Erythrobacter litoralis HTCC2594." Journal of Bacteriology 191, no. 7 (2009): 2419–20. http://dx.doi.org/10.1128/jb.00026-09.

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ABSTRACT Erythrobacter litoralis has been known as a bacteriochlorophyll a-containing, aerobic, anoxygenic, phototrophic bacterium. Here we announce the complete genome sequence of E. litoralis HTCC2594, which is devoid of phototrophic potential. E. litoralis HTCC2594, isolated by dilution-to-extinction culturing from seawater, could not carry out aerobic anoxygenic phototrophy and lacked genes for bacteriochlorophyll a biosynthesis and photosynthetic reaction center proteins.
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8

Ward, L. M., and Patrick M. Shih. "Phototrophy and carbon fixation in Chlorobi postdate the rise of oxygen." PLOS ONE 17, no. 8 (2022): e0270187. http://dx.doi.org/10.1371/journal.pone.0270187.

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While most productivity on the surface of the Earth today is fueled by oxygenic photosynthesis, for much of Earth history it is thought that anoxygenic photosynthesis—using compounds like ferrous iron or sulfide as electron donors—drove most global carbon fixation. Anoxygenic photosynthesis is still performed by diverse bacteria in niche environments today. Of these, the Chlorobi (formerly green sulfur bacteria) are often interpreted as being particularly ancient and are frequently proposed to have fueled the biosphere during late Archean and early Paleoproterozoic time before the rise of oxyg
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9

Wörmer, Lars, Niroshan Gajendra, Florence Schubotz, et al. "A micrometer‐scale snapshot on phototroph spatial distributions: mass spectrometry imaging of microbial mats in Octopus Spring, Yellowstone National Park." Geobiology 18, no. 6 (2020): 742–59. https://doi.org/10.1111/gbi.12411.

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<strong>Abstract</strong> Microbial mats from alkaline hot springs in the Yellowstone National Park are ideal natural laboratories to study photosynthetic life under extreme conditions, as well as the nuanced interactions of oxygenic and anoxygenic phototrophs. They represent distinctive examples of chlorophototroph (i.e., chlorophyll or bacteriochlorophyll‐based phototroph) diversity, and several novel phototrophs have been first described in these systems, all confined in space, coexisting and competing for niches defined by parameters such as light, oxygen, or temperature. In a novel approa
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10

Zander, Paul D., Stefanie B. Wirth, Adrian Gilli, Sandro Peduzzi, and Martin Grosjean. "Hyperspectral imaging sediment core scanning tracks high-resolution Holocene variations in (an)oxygenic phototrophic communities at Lake Cadagno, Swiss Alps." Biogeosciences 20, no. 12 (2023): 2221–35. http://dx.doi.org/10.5194/bg-20-2221-2023.

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Abstract. Pigments produced by anoxygenic phototrophic bacteria are valuable proxies of past anoxia in lacustrine and marine environments. Pigment measurement typically requires time-consuming and costly chemical extractions and chromatographic analyses, which limits the temporal resolution of paleoenvironmental reconstructions based on sedimentary pigments. Here, we evaluate the potential of in situ hyperspectral imaging (HSI) core scanning as a rapid, non-destructive method to document high-resolution changes in oxygenic and anoxygenic phototrophic communities at meromictic Lake Cadagno, Swi
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11

Kushkevych, I. V., and S. O. Hnatush. "The anoxygenic photosynthetic purple bacteria." Studia Biologica 4, no. 3 (2010): 137–54. http://dx.doi.org/10.30970/sbi.0403.116.

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12

Giraud, Eric, and André Verméglio. "Bacteriophytochromes in anoxygenic photosynthetic bacteria." Photosynthesis Research 97, no. 2 (2008): 141–53. http://dx.doi.org/10.1007/s11120-008-9323-0.

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13

Giraud, Eric, and André Verméglio. "Bacteriophytochromes in anoxygenic photosynthetic bacteria." Photosynthesis Research 97, no. 3 (2008): 263. http://dx.doi.org/10.1007/s11120-008-9362-6.

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14

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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15

Shabana, Effat F., and Gamila H. Ali. "Phytoplankton Activities in Hypersaline, Anoxic Conditions. II—Photosynthetic Activity of some Sulphide Adapted Cyanobacterial Strains Isolated from Solar Lake, Taba, Egypt." Water Science and Technology 40, no. 7 (1999): 127–32. http://dx.doi.org/10.2166/wst.1999.0344.

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Five cyanobacterial strains namely Oscillatoria limnetica, Aphanotheca stagnina, Synechococcus aeruginosus, Spirulina tenissima and Dactylococcopsis salina were isolated from an anaerobic sulphide rich hypersaline Solar Lake, Taba- Egypt. At oxygenic conditions Spirulina was the most tolerant strain to sulphide concentrations, while Aphanotheca and Synechococcus were the most sensitive. Aphanotheca have higher anoxygenic photoassimilation activity under a broad range of sulphide concentrations. The response of the five cyanobacterial strains to sulphide under oxygenic and anoxygenic conditions
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16

Batubara, U. M., R. D. Sibagariang, S. S. Siregar, et al. "Determination of Anoxygenic Photosynthetic Bacteria from Water and Sediment in Dumai Coastal Water, Indonesia." IOP Conference Series: Earth and Environmental Science 1118, no. 1 (2022): 012027. http://dx.doi.org/10.1088/1755-1315/1118/1/012027.

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Abstract Dumai is one of the coastal waters of Indonesia that has the potential for the biodiversity of microorganisms including anoxygenic photosynthetic bacteria (APB). Anoxygenic photosynthetic bacteria are bacteria that carry out decomposition activities even though oxygen levels in water and sediment are very little or even absent. This study aims to determine anoxygenic photosynthetic bacteria from aquatic and sedimentary ecosystems in the coastal waters of Dumai, Indonesia. This research was conducted by an experimental method using modified mineral media. The APB was isolated from six
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17

Wang, Xingzu, Kaiji Xie, Xiang Cheng, Yiwei Ren, and Chunli Wan. "Biofilm formation of anoxygenic photosynthetic bacteria induced by phototaxis for enhancing hydrogen production." Environmental Science: Water Research & Technology 1, no. 3 (2015): 383–93. http://dx.doi.org/10.1039/c5ew00019j.

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18

Ivanovsky, R. N., O. I. Keppen, N. V. Lebedeva, and D. S. Gruzdev. "Carbonic Anhydrase in Anoxygenic Phototrophic Bacteria." Microbiology 89, no. 3 (2020): 266–72. http://dx.doi.org/10.1134/s0026261720020058.

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19

Hanada, Satoshi. "Filamentous Anoxygenic Phototrophs in Hot Springs." Microbes and Environments 18, no. 2 (2003): 51–61. http://dx.doi.org/10.1264/jsme2.18.51.

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20

Sleep, Norman H., and Dennis K. Bird. "Evolutionary ecology during the rise of dioxygen in the Earth's atmosphere." Philosophical Transactions of the Royal Society B: Biological Sciences 363, no. 1504 (2008): 2651–64. http://dx.doi.org/10.1098/rstb.2008.0018.

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Pre-photosynthetic niches were meagre with a productivity of much less than 10 −4 of modern photosynthesis. Serpentinization, arc volcanism and ridge-axis volcanism reliably provided H 2 . Methanogens and acetogens reacted CO 2 with H 2 to obtain energy and make organic matter. These skills pre-adapted a bacterium for anoxygenic photosynthesis, probably starting with H 2 in lieu of an oxygen ‘acceptor’. Use of ferrous iron and sulphide followed as abundant oxygen acceptors, allowing productivity to approach modern levels. The ‘photobacterium’ proliferated rooting much of the bacterial tree. La
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21

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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22

Gest, Howard, and Robert E. Blankenship. "Time Line of Discoveries: Anoxygenic Bacterial Photosynthesis." Photosynthesis Research 80, no. 1-3 (2004): 59–70. http://dx.doi.org/10.1023/b:pres.0000030448.24695.ec.

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23

Widdel, Friedrich, Sylvia Schnell, Silke Heising, Armin Ehrenreich, Bernhard Assmus, and Bernhard Schink. "Ferrous iron oxidation by anoxygenic phototrophic bacteria." Nature 362, no. 6423 (1993): 834–36. http://dx.doi.org/10.1038/362834a0.

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24

Béjà, Oded, Marcelino T. Suzuki, John F. Heidelberg, et al. "Unsuspected diversity among marine aerobic anoxygenic phototrophs." Nature 415, no. 6872 (2002): 630–33. http://dx.doi.org/10.1038/415630a.

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25

Giraud, Eric, Joël Fardoux, Nicolas Fourrier, et al. "Bacteriophytochrome controls photosystem synthesis in anoxygenic bacteria." Nature 417, no. 6885 (2002): 202–5. http://dx.doi.org/10.1038/417202a.

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26

Griffin, B. M., J. Schott, and B. Schink. "Nitrite, an Electron Donor for Anoxygenic Photosynthesis." Science 316, no. 5833 (2007): 1870. http://dx.doi.org/10.1126/science.1139478.

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27

Atamna-Ismaeel, Nof, Omri Finkel, Fabian Glaser, et al. "Bacterial anoxygenic photosynthesis on plant leaf surfaces." Environmental Microbiology Reports 4, no. 2 (2012): 209–16. http://dx.doi.org/10.1111/j.1758-2229.2011.00323.x.

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28

Khanna, P., B. Rajkumar, and N. Jothikumar. "Anoxygenic degradation of aromatic substances byRhodopseudomonas palustris." Current Microbiology 25, no. 2 (1992): 63–67. http://dx.doi.org/10.1007/bf01570961.

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29

Imhoff, Johannes. "True marine and halophilic anoxygenic phototrophic bacteria." Archives of Microbiology 176, no. 4 (2001): 243–54. http://dx.doi.org/10.1007/s002030100326.

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Bundeleva, Irina A., Liudmila S. Shirokova, Pascale Bénézeth, Oleg S. Pokrovsky, Elena I. Kompantseva, and Stéphanie Balor. "Calcium carbonate precipitation by anoxygenic phototrophic bacteria." Chemical Geology 291 (January 2012): 116–31. http://dx.doi.org/10.1016/j.chemgeo.2011.10.003.

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Hiraishi, Akira, and Keizo Shimada. "Aerobic anoxygenic photosynthetic bacteria with zinc-bacteriochlorophyll." Journal of General and Applied Microbiology 47, no. 4 (2001): 161–80. http://dx.doi.org/10.2323/jgam.47.161.

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32

Kushkevych, Ivan, Veronika Bosáková, Monika Vítězová, and Simon K. M. R. Rittmann. "Anoxygenic Photosynthesis in Photolithotrophic Sulfur Bacteria and Their Role in Detoxication of Hydrogen Sulfide." Antioxidants 10, no. 6 (2021): 829. http://dx.doi.org/10.3390/antiox10060829.

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Hydrogen sulfide is a toxic compound that can affect various groups of water microorganisms. Photolithotrophic sulfur bacteria including Chromatiaceae and Chlorobiaceae are able to convert inorganic substrate (hydrogen sulfide and carbon dioxide) into organic matter deriving energy from photosynthesis. This process takes place in the absence of molecular oxygen and is referred to as anoxygenic photosynthesis, in which exogenous electron donors are needed. These donors may be reduced sulfur compounds such as hydrogen sulfide. This paper deals with the description of this metabolic process, repr
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33

Wang, Xingzu, Guihua Xu, Chunli Wan, Yiwei Ren, and Enling Tian. "Improved biomass production by humic analog anthraquinone-2-sulfonate from kitchen waste in a two-phase system." RSC Advances 6, no. 12 (2016): 9554–62. http://dx.doi.org/10.1039/c5ra18240a.

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The volatile fatty acids from kitchen waste were used as substrates of anoxygenic photosynthetic bacteria (APB) in a dark-photo fermentation reactor, and anthraquinone-2-sulfonate (AQS) was firstly applied to boost the biomass yield.
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34

Ward, Lewis M., and Patrick M. Shih. "Granick revisited: Synthesizing evolutionary and ecological evidence for the late origin of bacteriochlorophyll via ghost lineages and horizontal gene transfer." PLOS ONE 16, no. 1 (2021): e0239248. http://dx.doi.org/10.1371/journal.pone.0239248.

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Photosynthesis—both oxygenic and more ancient anoxygenic forms—has fueled the bulk of primary productivity on Earth since it first evolved more than 3.4 billion years ago. However, the early evolutionary history of photosynthesis has been challenging to interpret due to the sparse, scattered distribution of metabolic pathways associated with photosynthesis, long timescales of evolution, and poor sampling of the true environmental diversity of photosynthetic bacteria. Here, we reconsider longstanding hypotheses for the evolutionary history of phototrophy by leveraging recent advances in metagen
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35

Kushkevych, Ivan, Jiří Procházka, Márió Gajdács, Simon K. M. R. Rittmann, and Monika Vítězová. "Molecular Physiology of Anaerobic Phototrophic Purple and Green Sulfur Bacteria." International Journal of Molecular Sciences 22, no. 12 (2021): 6398. http://dx.doi.org/10.3390/ijms22126398.

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There are two main types of bacterial photosynthesis: oxygenic (cyanobacteria) and anoxygenic (sulfur and non-sulfur phototrophs). Molecular mechanisms of photosynthesis in the phototrophic microorganisms can differ and depend on their location and pigments in the cells. This paper describes bacteria capable of molecular oxidizing hydrogen sulfide, specifically the families Chromatiaceae and Chlorobiaceae, also known as purple and green sulfur bacteria in the process of anoxygenic photosynthesis. Further, it analyzes certain important physiological processes, especially those which are charact
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36

Saer, Rafael G., and Robert E. Blankenship. "Light harvesting in phototrophic bacteria: structure and function." Biochemical Journal 474, no. 13 (2017): 2107–31. http://dx.doi.org/10.1042/bcj20160753.

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This review serves as an introduction to the variety of light-harvesting (LH) structures present in phototrophic prokaryotes. It provides an overview of the LH complexes of purple bacteria, green sulfur bacteria (GSB), acidobacteria, filamentous anoxygenic phototrophs (FAP), and cyanobacteria. Bacteria have adapted their LH systems for efficient operation under a multitude of different habitats and light qualities, performing both oxygenic (oxygen-evolving) and anoxygenic (non-oxygen-evolving) photosynthesis. For each LH system, emphasis is placed on the overall architecture of the pigment–pro
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37

R., Saraswathi. "Isolation of Anoxygenic Phototrophic Bacteria from Soil and Water Samples." International Journal of Psychosocial Rehabilitation 23, no. 4 (2019): 1597–603. http://dx.doi.org/10.37200/ijpr/v23i4/pr190484.

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38

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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39

Ma, Jian, Katherine L. French, Xingqian Cui, Donald A. Bryant, and Roger E. Summons. "Carotenoid biomarkers in Namibian shelf sediments: Anoxygenic photosynthesis during sulfide eruptions in the Benguela Upwelling System." Proceedings of the National Academy of Sciences 118, no. 29 (2021): e2106040118. http://dx.doi.org/10.1073/pnas.2106040118.

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Aromatic carotenoid-derived hydrocarbon biomarkers are ubiquitous in ancient sediments and oils and are typically attributed to anoxygenic phototrophic green sulfur bacteria (GSB) and purple sulfur bacteria (PSB). These biomarkers serve as proxies for the environmental growth requirements of PSB and GSB, namely euxinic waters extending into the photic zone. Until now, prevailing models for environments supporting anoxygenic phototrophs include microbial mats, restricted basins and fjords with deep chemoclines, and meromictic lakes with shallow chemoclines. However, carotenoids have been report
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40

Yamada, Mitsunori, Hui Zhang, Satoshi Hanada, Kenji V. P. Nagashima, Keizo Shimada, and Katsumi Matsuura. "Structural and Spectroscopic Properties of a Reaction Center Complex from the Chlorosome-Lacking Filamentous Anoxygenic Phototrophic Bacterium Roseiflexus castenholzii." Journal of Bacteriology 187, no. 5 (2005): 1702–9. http://dx.doi.org/10.1128/jb.187.5.1702-1709.2005.

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ABSTRACT The photochemical reaction center (RC) complex of Roseiflexus castenholzii, which belongs to the filamentous anoxygenic phototrophic bacteria (green filamentous bacteria) but lacks chlorosomes, was isolated and characterized. The genes coding for the subunits of the RC and the light-harvesting proteins were also cloned and sequenced. The RC complex was composed of L, M, and cytochrome subunits. The cytochrome subunit showed a molecular mass of approximately 35 kDa, contained hemes c, and functioned as the electron donor to the photo-oxidized special pair of bacteriochlorophylls in the
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41

Rajasekhar, N., Ch Sasikala, and Ch V. Ramana. "Photoproduction of L‐tryptophan from indole and glycine by Rhodobacter sphaeroides OU5." Biotechnology and Applied Biochemistry 30, no. 3 (1999): 209–12. http://dx.doi.org/10.1111/j.1470-8744.1999.tb00772.x.

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A purple non‐sulphur anoxygenic phototrophic bacterium Rhodobacter sphaeroides could synthesize L‐tryptophan from indole and glycine with intermediate formation of D,L‐alanine and L‐serine. Presence of externally supplied keto acids has enhanced the rate and yields of L‐tryptophan photoproduction.
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42

Hernandez‐Maldonado, Jaime, Benjamin Sanchez‐Sedillo, Brendon Stoneburner, et al. "The genetic basis of anoxygenic photosynthetic arsenite oxidation." Environmental Microbiology 19, no. 1 (2016): 130–41. http://dx.doi.org/10.1111/1462-2920.13509.

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43

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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44

Gaju, N., V. Pavón, I. Marin, I. Esteve, R. Guerrero, and R. Amils. "Chromosome map of the phototrophic anoxygenic bacteriumChromatium vinosum." FEMS Microbiology Letters 126, no. 3 (1995): 241–47. http://dx.doi.org/10.1111/j.1574-6968.1995.tb07425.x.

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45

Hegler, F., and A. Kappler. "Cryopreservation of anoxygenic phototrophic Fe(II)-oxidizing bacteria." Cryobiology 61, no. 1 (2010): 158–60. http://dx.doi.org/10.1016/j.cryobiol.2010.04.001.

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46

Rashby, S. E., A. L. Sessions, R. E. Summons, and D. K. Newman. "Biosynthesis of 2-methylbacteriohopanepolyols by an anoxygenic phototroph." Proceedings of the National Academy of Sciences 104, no. 38 (2007): 15099–104. http://dx.doi.org/10.1073/pnas.0704912104.

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47

Lunina, O. N., I. A. Bryantseva, V. N. Akimov, et al. "Anoxygenic phototrophic bacterial community of Lake Shira (Khakassia)." Microbiology 76, no. 4 (2007): 469–79. http://dx.doi.org/10.1134/s0026261707040133.

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Crowe, S. A., J. A. Maresca, C. Jones, et al. "Deep-water anoxygenic photosythesis in a ferruginous chemocline." Geobiology 12, no. 4 (2014): 322–39. http://dx.doi.org/10.1111/gbi.12089.

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Koblížek, Michal. "Ecology of aerobic anoxygenic phototrophs in aquatic environments." FEMS Microbiology Reviews 39, no. 6 (2015): 854–70. http://dx.doi.org/10.1093/femsre/fuv032.

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Chandaravithoon, Piamsook, Siriporn Nakphet, and Raymond J. Ritchie. "Oxygenic and anoxygenic photosynthesis in a sewage pond." Journal of Applied Phycology 30, no. 6 (2018): 3089–102. http://dx.doi.org/10.1007/s10811-018-1432-3.

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