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Artículos de revistas sobre el tema "Heliobacteria"

Autor: Grafiati
Publicado: 4 de junio de 2021
Última modificación: 3 de febrero de 2022

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1

Sattley, W. Matthew, Michael T. Madigan, Wesley D. Swingley, et al. "The Genome of Heliobacterium modesticaldum, a Phototrophic Representative of the Firmicutes Containing the Simplest Photosynthetic Apparatus." Journal of Bacteriology 190, no. 13 (2008): 4687–96. http://dx.doi.org/10.1128/jb.00299-08.

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ABSTRACT Despite the fact that heliobacteria are the only phototrophic representatives of the bacterial phylum Firmicutes, genomic analyses of these organisms have yet to be reported. Here we describe the complete sequence and analysis of the genome of Heliobacterium modesticaldum, a thermophilic species belonging to this unique group of phototrophs. The genome is a single 3.1-Mb circular chromosome containing 3,138 open reading frames. As suspected from physiological studies of heliobacteria that have failed to show photoautotrophic growth, genes encoding enzymes for known autotrophic pathway
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2

Dewey, Emma D., Lynn M. Stokes, Brad M. Burchell, et al. "Analysis of the Complete Genome of the Alkaliphilic and Phototrophic Firmicute Heliorestis convoluta Strain HHT." Microorganisms 8, no. 3 (2020): 313. http://dx.doi.org/10.3390/microorganisms8030313.

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Despite significant interest and past work to elucidate the phylogeny and photochemistry of species of the Heliobacteriaceae, genomic analyses of heliobacteria to date have been limited to just one published genome, that of the thermophilic species Heliobacterium (Hbt.) modesticaldum str. Ice1T. Here we present an analysis of the complete genome of a second heliobacterium, Heliorestis (Hrs.) convoluta str. HHT, an alkaliphilic, mesophilic, and morphologically distinct heliobacterium isolated from an Egyptian soda lake. The genome of Hrs. convoluta is a single circular chromosome of 3.22 Mb wit
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3

Gest, Howard. "Discovery of the heliobacteria." Photosynthesis Research 41, no. 1 (1994): 17–21. http://dx.doi.org/10.1007/bf02184140.

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4

Bryantseva, I. A., V. M. Gorlenko, T. P. Tourova, et al. "Heliobacterium sulfidophilum sp. nov. andHeliobacterium undosum sp. nov.: Sulfideoxidizing heliobacteria from thermal sulfidic springs." Microbiology 69, no. 3 (2000): 325–34. http://dx.doi.org/10.1007/bf02756742.

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5

Beer-Romero, Peggy, Jeffrey L. Favinger, and Howard Gest. "Distinctive properties of bacilliform photosynthetic heliobacteria." FEMS Microbiology Letters 49, no. 3 (1988): 451–54. http://dx.doi.org/10.1111/j.1574-6968.1988.tb02774.x.

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6

Kimble, Linda K., Amy K. Stevenson, and Michael T. Madigan. "Chemotrophic growth of heliobacteria in darkness." FEMS Microbiology Letters 115, no. 1 (1994): 51–55. http://dx.doi.org/10.1111/j.1574-6968.1994.tb06613.x.

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7

Oh-oka, Hirozo. "Type 1 Reaction Center of Photosynthetic Heliobacteria†." Photochemistry and Photobiology 83, no. 1 (2007): 177–86. http://dx.doi.org/10.1562/2006-03-29-ir-860.

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8

Takaichi, Shinichi, Hirozo Oh-oka, Takashi Maoka, Deborah O. Jung, and Michael T. Madigan. "Novel carotenoid glucoside esters from alkaliphilic heliobacteria." Archives of Microbiology 179, no. 2 (2002): 95–100. http://dx.doi.org/10.1007/s00203-002-0504-5.

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9

Takaichi, Shinichi, Hirozo Oh-oka, Takashi Maoka, Deborah O. Jung, and Michael T. Madigan. "Novel carotenoid glucoside esters from alkaliphilic heliobacteria." Archives of Microbiology 179, no. 4 (2003): 305. http://dx.doi.org/10.1007/s00203-003-0536-5.

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10

Asao, Marie, and Michael T. Madigan. "Taxonomy, phylogeny, and ecology of the heliobacteria." Photosynthesis Research 104, no. 2-3 (2010): 103–11. http://dx.doi.org/10.1007/s11120-009-9516-1.

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11

Ducluzeau, A. L., E. Chenu, L. Capowiez, and F. Baymann. "The Rieske/cytochrome b complex of Heliobacteria." Biochimica et Biophysica Acta (BBA) - Bioenergetics 1777, no. 9 (2008): 1140–46. http://dx.doi.org/10.1016/j.bbabio.2008.04.026.

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12

Kimble, Linda K., and Michael T. Madigan. "Nitrogen fixation and nitrogen metabolism in heliobacteria." Archives of Microbiology 158, no. 3 (1992): 155–61. http://dx.doi.org/10.1007/bf00290810.

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13

Ormerod, John G., Linda K. Kimble, Tore Nesbakken, Yngve A. Torgersen, Carl R. Woese, and Michael T. Madigan. "Heliophilum fasciatum gen. nov. sp. nov. and Heliobacterium gestii sp. nov.: endospore-forming heliobacteria from rice field soils." Archives of Microbiology 165, no. 4 (1996): 226–34. http://dx.doi.org/10.1007/s002030050320.

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14

Amesz, Jan. "The heliobacteria, a new group of photosynthetic bacteria." Journal of Photochemistry and Photobiology B: Biology 30, no. 2-3 (1995): 89–96. http://dx.doi.org/10.1016/1011-1344(95)07207-i.

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15

Nozawa, Tsunenori. "A Report from ESF Workshop on Green and Heliobacteria." TRENDS IN THE SCIENCES 3, no. 2 (1998): 82–83. http://dx.doi.org/10.5363/tits.3.2_82.

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16

Olson, J. M. "European Science Foundation Workshop on Green Bacteria and Heliobacteria." Photosynthetica 35, no. 1 (1997): 155–57. http://dx.doi.org/10.1023/a:1006898521099.

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17

Francke, Christof, Stephan C. M. Otte, Jos C. van der Heiden, and Jan Amesz. "Spurious circular dichroism signals with intact cells of heliobacteria." Biochimica et Biophysica Acta (BBA) - Bioenergetics 1186, no. 1-2 (1994): 75–80. http://dx.doi.org/10.1016/0005-2728(94)90137-6.

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18

Bryant, Donald A. "Gene nomenclature recommendations for green photosynthetic bacteria and heliobacteria." Photosynthesis Research 41, no. 1 (1994): 27–28. http://dx.doi.org/10.1007/bf02184142.

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19

Vermaas, Wim F. J. "Evolution of heliobacteria: Implications for photosynthetic reaction center complexes." Photosynthesis Research 41, no. 1 (1994): 285–94. http://dx.doi.org/10.1007/bf02184169.

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20

Girija, K. R., B. Vinay, Ch Sasikala, and Ch V. Ramana. "Novel heliobacteria of a few semi-arid tropical soils." Indian Journal of Microbiology 50, S1 (2010): 17–20. http://dx.doi.org/10.1007/s12088-010-0069-y.

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21

Pickett, Mark W., Michael P. Williamson, and David J. Kelly. "An enzyme and13C-NMR study of carbon metabolism in heliobacteria." Photosynthesis Research 41, no. 1 (1994): 75–88. http://dx.doi.org/10.1007/bf02184147.

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22

Kobayashi, Masami, Erik Jan van de Meent, Cornelis Erkelens, Jan Amesz, Isamu Ikegami, and Tadashi Watanabe. "Bacteriochlorophyll g epimer as a possible reaction center component of heliobacteria." Biochimica et Biophysica Acta (BBA) - Bioenergetics 1057, no. 1 (1991): 89–96. http://dx.doi.org/10.1016/s0005-2728(05)80087-8.

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23

Pickett, Mark W., Norbert Weiss, and David J. Kelly. "Gram-positive cell wall structure of the A3γ type in heliobacteria." FEMS Microbiology Letters 122, no. 1-2 (1994): 7–12. http://dx.doi.org/10.1111/j.1574-6968.1994.tb07135.x.

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24

van de Meent, Erik Jan, Frank A. M. Kleinherenbrink, and Jan Amesz. "Purification and properties of an antenna-reaction center complex from heliobacteria." Biochimica et Biophysica Acta (BBA) - Bioenergetics 1015, no. 2 (1990): 223–30. http://dx.doi.org/10.1016/0005-2728(90)90024-x.

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25

Kimble-Long, Linda K., and Michael T. Madigan. "Molecular evidence that the capacity for endosporulation is universal among phototrophic heliobacteria." FEMS Microbiology Letters 199, no. 2 (2001): 191–95. http://dx.doi.org/10.1111/j.1574-6968.2001.tb10673.x.

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26

Lavoie, Noémie C., Daniel S. Grégoire, Bejamin R. Stenzler, and Alexandre J. Poulain. "Reduced sulphur sources favour Hg II reduction during anoxygenic photosynthesis by Heliobacteria." Geobiology 18, no. 1 (2019): 70–79. http://dx.doi.org/10.1111/gbi.12364.

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27

van de Meent, Erik Jan, Masami Kobayashi, Cornelis Erkelens, Peter A. van Veelen, Jan Amesz, and Tadashi Watanabe. "Identification of 81-hydroxychlorophyll a as a functional reaction center pigment in heliobacteria." Biochimica et Biophysica Acta (BBA) - Bioenergetics 1058, no. 3 (1991): 356–62. http://dx.doi.org/10.1016/s0005-2728(05)80131-8.

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28

Grégoire, D. S., N. C. Lavoie, and A. J. Poulain. "Heliobacteria Reveal Fermentation As a Key Pathway for Mercury Reduction in Anoxic Environments." Environmental Science & Technology 52, no. 7 (2018): 4145–53. http://dx.doi.org/10.1021/acs.est.8b00320.

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29

Tang, Kuo-Hsiang, Xueyang Feng, Wei-Qin Zhuang, Lisa Alvarez-Cohen, Robert E. Blankenship, and Yinjie J. Tang. "Carbon Flow of Heliobacteria Is Related More toClostridiathan to the Green Sulfur Bacteria." Journal of Biological Chemistry 285, no. 45 (2010): 35104–12. http://dx.doi.org/10.1074/jbc.m110.163303.

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30

Xiong, Jin, Carl E. Bauer, and Anjly Pancholy. "Insight into the haem d 1 biosynthesis pathway in heliobacteria through bioinformatics analysis." Microbiology 153, no. 10 (2007): 3548–62. http://dx.doi.org/10.1099/mic.0.2007/007930-0.

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31

Enkh-Amgalan, Jigjiddorj, Hiroko Kawasaki, and Tatsuji Seki. "NifH and NifD sequences of heliobacteria: a new lineage in the nitrogenase phylogeny." FEMS Microbiology Letters 243, no. 1 (2005): 73–79. http://dx.doi.org/10.1016/j.femsle.2004.11.044.

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32

van der Est, A., C. Hager-Braun, W. Leibl, G. Hauska, and D. Stehlik. "Transient electron paramagnetic resonance spectroscopy on green-sulfur bacteria and heliobacteria at two microwave frequencies." Biochimica et Biophysica Acta (BBA) - Bioenergetics 1409, no. 2 (1998): 87–98. http://dx.doi.org/10.1016/s0005-2728(98)00152-2.

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33

Kimble-Long, L. K., and M. T. Madigan. "Irradiance Effects on Growth and Bacteriochlorophyll Content of Phototrophic Heliobacteria, Purple and Green Photosynthetic Bacteria." Photosynthetica 40, no. 4 (2002): 629–32. http://dx.doi.org/10.1023/a:1024324707721.

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34

Azai, Chihiro, Yusuke Tsukatani, Shigeru Itoh, and Hirozo Oh-oka. "C-type cytochromes in the photosynthetic electron transfer pathways in green sulfur bacteria and heliobacteria." Photosynthesis Research 104, no. 2-3 (2010): 189–99. http://dx.doi.org/10.1007/s11120-009-9521-4.

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35

Sattley, W. Matthew, and Robert E. Blankenship. "Insights into heliobacterial photosynthesis and physiology from the genome of Heliobacterium modesticaldum." Photosynthesis Research 104, no. 2-3 (2010): 113–22. http://dx.doi.org/10.1007/s11120-010-9529-9.

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36

Asao, Marie, Shinichi Takaichi, and Michael T. Madigan. "Amino acid-assimilating phototrophic heliobacteria from soda lake environments: Heliorestis acidaminivorans sp. nov. and ‘Candidatus Heliomonas lunata’." Extremophiles 16, no. 4 (2012): 585–95. http://dx.doi.org/10.1007/s00792-012-0458-8.

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37

Thamarath, Smitha Surendran, A. Alia, Eugenio Daviso, Deni Mance, John H. Golbeck, and Jörg Matysik. "Whole Cell Nuclear Magnetic Resonance Characterization of Two Photochemically Active States of the Photosynthetic Reaction Center in Heliobacteria." Biochemistry 51, no. 29 (2012): 5763–73. http://dx.doi.org/10.1021/bi300468y.

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38

Noguchi, Takumi. "Fourier transform infrared spectroscopy of special pair bacteriochlorophylls in homodimeric reaction centers of heliobacteria and green sulfur bacteria." Photosynthesis Research 104, no. 2-3 (2010): 321–31. http://dx.doi.org/10.1007/s11120-009-9509-0.

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39

Takaichi, S., Kazuhito Inoue, Mitsuhiro Akaike, Masami Kobayashi, Hirozo Oh-oka, and Michael T. Madigan. "The major carotenoid in all known species of heliobacteria is the C 30 carotenoid 4,4′-diaponeurosporene, not neurosporene." Archives of Microbiology 168, no. 4 (1997): 277–81. http://dx.doi.org/10.1007/s002030050499.

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40

Aase, Brit, Erik Jantzen, Klaus Bryn, and John Ormerod. "Lipids of heliobacteria are characterised by a high proportion of monoenoic fatty acids with variable double bond positions." Photosynthesis Research 41, no. 1 (1994): 67–74. http://dx.doi.org/10.1007/bf02184146.

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41

Heathcote, Peter, Michael R. Jones, and Paul K. Fyfe. "Type I photosynthetic reaction centres: structure and function." Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences 358, no. 1429 (2003): 231–43. http://dx.doi.org/10.1098/rstb.2002.1178.

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We review recent advances in the study of the photosystem I reaction centre, following the determination of a spectacular 2.5 Å resolution crystal structure for this complex of Synechococcus elongatus . Photosystem I is proving different to type II reaction centres in structure and organization, and the mechanism of transmembrane electron transfer, and is providing insights into the control of function in reaction centres that operate at very low redox potentials. The photosystem I complex of oxygenic organisms has a counterpart in non–oxygenic bacteria, the strictly anaerobic phototrophic gre
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42

Trost, Jeffrey T., Daniel C. Brune, and Robert E. Blankenship. "Protein sequences and redox titrations indicate that the electron acceptors in reaction centers from heliobacteria are similar to Photosystem I." Photosynthesis Research 32, no. 1 (1992): 11–22. http://dx.doi.org/10.1007/bf00028794.

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43

Thompson, Mark A., and Jack Fajer. "Calculations of bacteriochlorophyll g primary donors in photosynthetic heliobacteria: how to shift the energy of a phototrap by 2000 cm-1." Journal of Physical Chemistry 96, no. 7 (1992): 2933–35. http://dx.doi.org/10.1021/j100186a031.

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44

Muhiuddin, Irine P., Stephen E. J. Rigby, Michael C. W. Evans, Jan Amesz, and Peter Heathcote. "ENDOR and Special TRIPLE Resonance Spectroscopy of Photoaccumulated Semiquinone Electron Acceptors in the Reaction Centers of Green Sulfur Bacteria and Heliobacteria†." Biochemistry 38, no. 22 (1999): 7159–67. http://dx.doi.org/10.1021/bi982042u.

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45

Kimura, Akihiro, Hirotaka Kitoh-Nishioka, Yasuteru Shigeta, and Shigeru Itoh. "Comparison between the Light-Harvesting Mechanisms of Type-I Photosynthetic Reaction Centers of Heliobacteria and Photosystem I: Pigment Site Energy Distribution and Exciton State." Journal of Physical Chemistry B 125, no. 15 (2021): 3727–38. http://dx.doi.org/10.1021/acs.jpcb.0c09400.

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46

Heinnickel, Mark, and John H. Golbeck. "Heliobacterial photosynthesis." Photosynthesis Research 92, no. 1 (2007): 35–53. http://dx.doi.org/10.1007/s11120-007-9162-4.

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47

Baymann, F., and W. Nitschke. "Heliobacterial Rieske/cytb complex." Photosynthesis Research 104, no. 2-3 (2010): 177–87. http://dx.doi.org/10.1007/s11120-009-9524-1.

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48

Kimble, Linda K., Linda Mandelco, Carl R. Woese, and Michael T. Madigan. "Heliobacterium modesticaldum, sp. nov., a thermophilic heliobacterium of hot springs and volcanic soils." Archives of Microbiology 163, no. 4 (1995): 259–67. http://dx.doi.org/10.1007/bf00393378.

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49

Kimble, Linda K., Linda Mandelco, Carl R. Woese, and M. T. Madigan. "Heliobacterium modesticaldum, sp. nov., a thermophilic heliobacterium of hot springs and volcanic soils." Archives of Microbiology 163, no. 4 (1995): 259–67. http://dx.doi.org/10.1007/s002030050202.

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50

Rexroth, Sascha, David Ranava, Wolfgang Nitschke, and Frauke Baymann. "Butyrate metabolism in Heliobacterium modesticaldum ?" Biochimica et Biophysica Acta (BBA) - Bioenergetics 1857 (August 2016): e90-e91. http://dx.doi.org/10.1016/j.bbabio.2016.04.295.

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