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1

Oren, Aharon. "Bioenergetic Aspects of Halophilism." Microbiology and Molecular Biology Reviews 63, no. 2 (June 1, 1999): 334–48. http://dx.doi.org/10.1128/mmbr.63.2.334-348.1999.

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SUMMARY Examinination of microbial diversity in environments of increasing salt concentrations indicates that certain types of dissimilatory metabolism do not occur at the highest salinities. Examples are methanogenesis for H2 + CO2 or from acetate, dissimilatory sulfate reduction with oxidation of acetate, and autotrophic nitrification. Occurrence of the different metabolic types is correlated with the free-energy change associated with the dissimilatory reactions. Life at high salt concentrations is energetically expensive. Most bacteria and also the methanogenic archaea produce high intrace
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2

Loo, C. Y., D. A. Corliss, and N. Ganeshkumar. "Streptococcus gordonii Biofilm Formation: Identification of Genes that Code for Biofilm Phenotypes." Journal of Bacteriology 182, no. 5 (March 1, 2000): 1374–82. http://dx.doi.org/10.1128/jb.182.5.1374-1382.2000.

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ABSTRACT Viridans streptococci, which include Streptococcus gordonii, are pioneer oral bacteria that initiate dental plaque formation. Sessile bacteria in a biofilm exhibit a mode of growth that is distinct from that of planktonic bacteria. Biofilm formation ofS. gordonii Challis was characterized using an in vitro biofilm formation assay on polystyrene surfaces. The same assay was used as a nonbiased method to screen isogenic mutants generated by Tn916 transposon mutagenesis for defective biofilm formation. Biofilms formed optimally when bacteria were grown in a minimal medium under anaerobic
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3

St-Arnaud, S., J. G. Bisaillon, and R. Beaudet. "Microbiological aspects of ammonia oxidation of swine waste." Canadian Journal of Microbiology 37, no. 12 (December 1, 1991): 918–23. http://dx.doi.org/10.1139/m91-159.

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Ammonia-oxidizing bacteria were present at 102 MPN/mL (most probable number per millilitre) in swine waste, and they were outnumbered by a factor of 105 by the heterotrophs of the indigenous flora. To study these ammonia-oxidizing bacteria we attempted to isolate them in pure culture. We succeeded in increasing the concentration of these bacteria by successive transfers to an inorganic medium, but the heterotrophs were always dominant. To overcome this problem Nitrosomonas europaea ATCC 19718 was adapted to grow in stabilized swine waste. With this adapted strain it was shown that the number o
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4

Anandkumar, Balakrishnan, Rani P. George, Sundaram Maruthamuthu, Natarajan Parvathavarthini, and Uthandi Kamachi Mudali. "Corrosion characteristics of sulfate-reducing bacteria (SRB) and the role of molecular biology in SRB studies: an overview." Corrosion Reviews 34, no. 1-2 (March 1, 2016): 41–63. http://dx.doi.org/10.1515/corrrev-2015-0055.

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AbstractSulfate-reducing bacteria (SRB), an anaerobic bacterial group, are found in many environments like freshwater, marine sediments, agricultural soil, and oil wells where sulfate is present. SRB derives energy from electron donors such as sulfate, elemental sulfur or metals, and fermenting nitrate. It is the major bacterial group involved in the microbiologically influenced corrosion (MIC), souring, and biofouling problems in oil-gas-producing facilities as well as transporting and storage facilities. SRB utilizes sulfate ions as an electron acceptor and produce H2S, which is an agent of
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5

Damianovic, M. H. R. Z., I. K. Sakamoto, and E. Foresti. "Biofilm adaptation to sulfate reduction in anaerobic immobilized biomass reactors sujected to different COD/sulfate ratios." Water Science and Technology 54, no. 2 (July 1, 2006): 119–26. http://dx.doi.org/10.2166/wst.2006.494.

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Various aspects of biofilm adaptation to sulfate reduction in horizontal-flow anaerobic immobilized biomass (HAIB) reactors subjected to increasing sulfate concentrations and different COD/sulfate ratios are presented and discussed. Four bench-scale HAIB reactors filled with vegetal carbon (R1 and R2) and polyurethane foam matrices (R3 and R4) were utilized. Influent sulfate concentrations ranging from 500 to 3000 mg/L were applied at COD/sulfate ratios ranging from 5.0 to 1.7. Reactors R1 and R4 were operated with higher sulfate loads than those applied to R2 and R3. For the same COD/sulfate
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6

Katsenos, Stamatis, Iosif Galinos, Panagiota Styliara, Nikoletta Galanopoulou, and Konstantinos Psathakis. "Primary Bronchopulmonary Actinomycosis Masquerading as Lung Cancer: Apropos of Two Cases and Literature Review." Case Reports in Infectious Diseases 2015 (2015): 1–5. http://dx.doi.org/10.1155/2015/609637.

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Actinomycosis is a rare and slowly progressive infectious disease that can affect a variety of organ systems including the lung. It is caused by filamentous Gram-positive anaerobic bacteria of the genusActinomyces. Despite its rarity, pulmonary actinomycosis can involve lung parenchyma, bronchial structures, and chest wall. The disease can mimic lung malignancy given its nonspecific clinical and radiological presentation, thus posing a diagnostic dilemma to the attending physician. In this paper, we describe two patients with pulmonary actinomycosis mimicking bronchogenic carcinoma; the former
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7

Kelm, Matthias, Simon Kusan, Güzin Surat, Friedrich Anger, Joachim Reibetanz, Christoph-Thomas Germer, Nicolas Schlegel, and Sven Flemming. "Disease- and Medication-Specific Differences of the Microbial Spectrum in Perianal Fistulizing Crohn’s Disease—Relevant Aspects for Antibiotic Therapy." Biomedicines 10, no. 11 (October 23, 2022): 2682. http://dx.doi.org/10.3390/biomedicines10112682.

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Perianal fistulizing Crohn’s Disease (CD) with abscess formation represents an aggressive phenotype in Inflammatory Bowel Disease (IBD) with increased morbidity. Treatment is multidisciplinary and includes antibiotics, but knowledge about the microbial spectrum is rare often resulting in inadequate antimicrobial therapy. In this single center retrospective study, all patients who were operated due to perianal abscess formation were retrospectively analyzed and the microbial spectrum evaluated. Patients were divided into a CD and non-CD group with further subgroup analysis. 138 patients were fi
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8

Ksembaev, Said, Elena Nesterova, Ol'ga Torgashova, Elima Agatieva, and Dinar Busheev. "ETHIOPATHOGENETIC ASPECTS ACUTE ODONTOGENIC INFECTION." Actual problems in dentistry 17, no. 2 (August 12, 2021): 19–26. http://dx.doi.org/10.18481/2077-7566-20-17-2-19-26.

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Subject. A review of the literature on the topical problem of dentistry — the etiology and pathogenesis of acute odontogenic purulent-inflammatory diseases is presented.
 The purpose of the research is to study the materials of publications. dedicated to the etiopathogenetic aspects of acute odontogenic infection.
 Methodology. The etiology and pathogenesis of acute odontogenic purulent-inflammatory diseases are described in detail, in the light of modern concepts.
 Results. The unfavorable factors influencing the increase in the frequency of acute odontogenic purulent-inflammat
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9

Bauer, Carl, Sylvie Elsen, Lee R. Swem, Danielle L. Swem, and Shinji Masuda. "Redox and light regulation of gene expression in photosynthetic prokaryotes." Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences 358, no. 1429 (January 29, 2003): 147–54. http://dx.doi.org/10.1098/rstb.2002.1189.

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All photosynthetic organisms control expression of photosynthesis genes in response to alterations in light intensity as well as to changes in cellular redox potential. Light regulation in plants involves a well–defined set of red– and blue–light absorbing photoreceptors called phytochrome and cryptochrome. Less understood are the factors that control synthesis of the plant photosystem in response to changes in cellular redox. Among a diverse set of photosynthetic bacteria the best understood regulatory systems are those synthesized by the photosynthetic bacterium Rhodobacter capsulatus . This
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10

Vinga, S., A. R. Neves, H. Santos, B. W. Brandt, and S. A. L. M. Kooijman. "Subcellular metabolic organization in the context of dynamic energy budget and biochemical systems theories." Philosophical Transactions of the Royal Society B: Biological Sciences 365, no. 1557 (November 12, 2010): 3429–42. http://dx.doi.org/10.1098/rstb.2010.0156.

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The dynamic modelling of metabolic networks aims to describe the temporal evolution of metabolite concentrations in cells. This area has attracted increasing attention in recent years owing to the availability of high-throughput data and the general development of systems biology as a promising approach to study living organisms. Biochemical Systems Theory (BST) provides an accurate formalism to describe biological dynamic phenomena. However, knowledge about the molecular organization level, used in these models, is not enough to explain phenomena such as the driving forces of these metabolic
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11

Thorakkattu, Priyamvada, Anandu Chandra Khanashyam, Kartik Shah, Karthik Sajith Babu, Anjaly Shanker Mundanat, Aiswariya Deliephan, Gitanjali S. Deokar, Chalat Santivarangkna, and Nilesh Prakash Nirmal. "Postbiotics: Current Trends in Food and Pharmaceutical Industry." Foods 11, no. 19 (October 5, 2022): 3094. http://dx.doi.org/10.3390/foods11193094.

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Postbiotics are non-viable bacterial products or metabolic byproducts produced by probiotic microorganisms that have biologic activity in the host. Postbiotics are functional bioactive compounds, generated in a matrix during anaerobic fermentation of organic nutrients like prebiotics, for the generation of energy in the form of adenosine triphosphate. The byproducts of this metabolic sequence are called postbiotics, these are low molecular weight soluble compounds either secreted by live microflora or released after microbial cell lysis. A few examples of widely studied postbiotics are short-c
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12

Maas, Lori K., and Thomas L. Glass. "Cellobiose uptake by the cellulolytic ruminai anaerobe Fibrobacter (Bacteroides) succinogenes." Canadian Journal of Microbiology 37, no. 2 (February 1, 1991): 141–47. http://dx.doi.org/10.1139/m91-021.

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Cellobiose transport by the cellulolytic ruminal anaerobe Fibrobacter (Bacteroides) succinogenes was measured using randomly tritiated cellobiose. When assayed at the same concentration (1 mM), total cellobiose uptake was one-fourth to one-third that of total glucose uptake. The abilities of F. succinogenes to transport cellobiose or glucose were not affected by the sugar on which the cells were grown. Aspects of the simultaneous transport of [14C(U)]glucose and [3H(G)]cellobiose, the failure of high concentrations of cold glucose to compete with hypothetical [3H(G)] glucose (derived externall
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13

Krüger, Larissa, Christina Herzberg, Hermann Rath, Tiago Pedreira, Till Ischebeck, Anja Poehlein, Jan Gundlach, et al. "Essentiality of c-di-AMP in Bacillus subtilis: Bypassing mutations converge in potassium and glutamate homeostasis." PLOS Genetics 17, no. 1 (January 22, 2021): e1009092. http://dx.doi.org/10.1371/journal.pgen.1009092.

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In order to adjust to changing environmental conditions, bacteria use nucleotide second messengers to transduce external signals and translate them into a specific cellular response. Cyclic di-adenosine monophosphate (c-di-AMP) is the only known essential nucleotide second messenger. In addition to the well-established role of this second messenger in the control of potassium homeostasis, we observed that glutamate is as toxic as potassium for a c-di-AMP-free strain of the Gram-positive model bacterium Bacillus subtilis. In this work, we isolated suppressor mutants that allow growth of a c-di-
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14

Finegold, Sydney M., and Hannele Jousimies–Somer. "Recently Described Clinically Important Anaerobic Bacteria: Medical Aspects." Clinical Infectious Diseases 25, s2 (September 1997): S88—S93. http://dx.doi.org/10.1086/516237.

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15

Kapatral, Vinayak, Iain Anderson, Natalia Ivanova, Gary Reznik, Tamara Los, Athanasios Lykidis, Anamitra Bhattacharyya, et al. "Genome Sequence and Analysis of the Oral Bacterium Fusobacterium nucleatum Strain ATCC 25586." Journal of Bacteriology 184, no. 7 (April 1, 2002): 2005–18. http://dx.doi.org/10.1128/jb.184.7.2005-2018.2002.

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ABSTRACT We present a complete DNA sequence and metabolic analysis of the dominant oral bacterium Fusobacterium nucleatum. Although not considered a major dental pathogen on its own, this anaerobe facilitates the aggregation and establishment of several other species including the dental pathogens Porphyromonas gingivalis and Bacteroides forsythus. The F. nucleatum strain ATCC 25586 genome was assembled from shotgun sequences and analyzed using the ERGO bioinformatics suite (http://www.integratedgenomics.com ). The genome contains 2.17 Mb encoding 2,067 open reading frames, organized on a sing
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16

Srečnik, Špela, Irena Zdovc, Urška Javoršek, Tina Pirš, Zlatko Pavlica, and Ana Nemec. "Microbiological Aspects of Naturally Occurring Primary Endodontic Infections in Dogs." Journal of Veterinary Dentistry 36, no. 2 (June 2019): 124–28. http://dx.doi.org/10.1177/0898756419873639.

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Dental fractures are common in dogs, but data on microbiology of naturally occurring primary endodontic infections, and their relation to clinical and radiographic signs, are lacking. Samples were obtained from root canals of 32 periodontally healthy fractured teeth under aseptic conditions and immediately cultured for aerobic and anaerobic bacteria. Cultures were further identified by matrix-assisted laser desorption/ionization, time of flight technology. Sixty-one bacteria (30 bacterial species) were isolated from root canals; 54% were Gram-negative bacteria, 53% were facultative anaerobic,
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17

Jousimies–Somer, Hannele. "Recently Described Clinically Important Anaerobic Bacteria: Taxonomic Aspects and Update." Clinical Infectious Diseases 25, s2 (September 1997): S78—S87. http://dx.doi.org/10.1086/516227.

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18

Zhilina, Tatyana N., and George A. Zavarzin. "Extremely halophilic, methylotrophic, anaerobic bacteria." FEMS Microbiology Letters 87, no. 3-4 (December 1990): 315–22. http://dx.doi.org/10.1111/j.1574-6968.1990.tb04930.x.

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19

Buckel, Wolfgang. "Unusual dehydrations in anaerobic bacteria." FEMS Microbiology Letters 88, no. 3-4 (June 1992): 211–32. http://dx.doi.org/10.1111/j.1574-6968.1992.tb04989.x.

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20

Antranikian, Garabed, and Friedrich Giffhorn. "Citrate metabolism in anaerobic bacteria." FEMS Microbiology Letters 46, no. 2 (June 1987): 175–98. http://dx.doi.org/10.1111/j.1574-6968.1987.tb02458.x.

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21

Oh, Herin, Maria Hedberg, David Wade, and Charlotta Edlund. "Activities of Synthetic Hybrid Peptides against Anaerobic Bacteria: Aspects of Methodology and Stability." Antimicrobial Agents and Chemotherapy 44, no. 1 (January 1, 2000): 68–72. http://dx.doi.org/10.1128/aac.44.1.68-72.2000.

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ABSTRACT The increasing problem of antibiotic resistance among pathogenic bacteria requires development of new antimicrobial agents. One line of investigation is the synthesis of antimicrobial hybrid peptides. The aim of the present investigation was to determine the in vitro activities of 16 cecropin-melittin hybrid peptides (CAMEL analogues) against 60 anaerobic bacterial strains, to compare their activities with those of seven clinically used antimicrobial agents, and to compare different methods for anaerobic susceptibility testing of these peptides. The stability of one of the peptides, t
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22

Kato, Naoki, and Haru Kato. "Molecular Detection and Identification of Anaerobic Bacteria." Journal of Infection and Chemotherapy 3, no. 1 (1997): 5–14. http://dx.doi.org/10.1007/bf02489178.

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23

Zhao, Tianyuan, Jungyul Song, Yuzhuo Ping, and Meihua Li. "The Application of Antimicrobial Photodynamic Therapy (aPDT) in the Treatment of Peri-Implantitis." Computational and Mathematical Methods in Medicine 2022 (May 12, 2022): 1–8. http://dx.doi.org/10.1155/2022/3547398.

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Background. This literature review evaluates the mechanisms and efficacy of different types of antimicrobial photodynamic therapy (aPDT) for treating peri-implantitis by reviewing existing experimental studies to provide guidance for the clinical application of antibacterial photodynamic therapy (aPDT) in oral implants. Materials and Methods. From February 2001 to February 2021, we have collected 152 randomized controlled trials of aPDT for peri-implantitis by searching the experimental studies and clinical trials published in PubMed, Embase, Web of Science, and Google Scholar databases via on
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24

Urbán, Edit, and Márió Gajdács. "Microbiological and Clinical Aspects of Actinomyces Infections: What Have We Learned?" Antibiotics 10, no. 2 (February 3, 2021): 151. http://dx.doi.org/10.3390/antibiotics10020151.

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25

Cervantes, Francisco J., and André B. Dos Santos. "Reduction of azo dyes by anaerobic bacteria: microbiological and biochemical aspects." Reviews in Environmental Science and Bio/Technology 10, no. 2 (January 19, 2011): 125–37. http://dx.doi.org/10.1007/s11157-011-9228-9.

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26

Ramos, Antonio. "Sternoclavicular Joint Infection Caused by Anaerobic Bacteria." JONA's Healthcare Law, Ethics, and Regulation 1, no. 4 (December 1999): 309–10. http://dx.doi.org/10.1097/00128488-199912000-00009.

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27

Diekert, Gabriele. "CO2reduction to acetate in anaerobic bacteria." FEMS Microbiology Letters 87, no. 3-4 (December 1990): 391–96. http://dx.doi.org/10.1111/j.1574-6968.1990.tb04942.x.

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28

Andersen, I., and H. P. Olesen. "Anaerobic bacteria in rheumatoid arthritis." Annals of the Rheumatic Diseases 49, no. 7 (July 1, 1990): 568. http://dx.doi.org/10.1136/ard.49.7.568-b.

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29

Morris, J. Gareth. "Obligately anaerobic bacteria in biotechnology." Applied Biochemistry and Biotechnology 48, no. 2 (August 1994): 75–106. http://dx.doi.org/10.1007/bf02796164.

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30

Lubbe, Maria M., Kim Stanley, and Lynda J. Chalkley. "Prevalence ofnimgenes in anaerobic/facultative anaerobic bacteria isolated in South Africa." FEMS Microbiology Letters 172, no. 1 (March 1999): 79–83. http://dx.doi.org/10.1111/j.1574-6968.1999.tb13453.x.

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31

Fernandez, Fresia, and Matthew D. Collins. "Vitamin K composition of anaerobic gut bacteria." FEMS Microbiology Letters 41, no. 2 (April 1987): 175–80. http://dx.doi.org/10.1111/j.1574-6968.1987.tb02191.x.

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32

Buckel, Wolfgang, Berta M. Martins, Albrecht Messerschmidt, and Bernard T. Golding. "Radical-mediated dehydration reactions in anaerobic bacteria." Biological Chemistry 386, no. 10 (October 1, 2005): 951–59. http://dx.doi.org/10.1515/bc.2005.111.

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AbstractMost dehydratases catalyse the elimination of water from β-hydroxy ketones, β-hydroxy carboxylic acids or β-hydroxyacyl-CoA. The electron-withdrawing carbonyl functionalities acidify the α-hydrogens to enable their removal by basic amino acid side chains. Anaerobic bacteria, however, ferment amino acids via α- or γ-hydroxyacyl-CoA, dehydrations of which involve the abstraction of a β-hydrogen, which is ostensibly non-acidic (pKca. 40). Evidence is accumulating that β-hydrogens are acidified via transient conversion of the CoA derivatives to enoxy radicals by one-electron transfers, whi
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33

van Bruggen, J. J. A., K. B. Zwart, C. K. Stumm, and G. D. Vogels. "Symbiosis of methanogenic bacteria and anaerobic ciliates." Antonie van Leeuwenhoek 51, no. 4 (July 1985): 452–53. http://dx.doi.org/10.1007/bf02275078.

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34

LAMM, Lydia, Gernot HECKMANN, and Paul RENZ. "Biosynthesis of Vitamin B12 in Anaerobic Bacteria." European Journal of Biochemistry 122, no. 3 (March 3, 2005): 569–71. http://dx.doi.org/10.1111/j.1432-1033.1982.tb06476.x.

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35

van Bruggen, J. J. A., C. K. Stumm, and G. D. Vogels. "A novel anaerobic amoeba with endosymbiotic bacteria." Antonie van Leeuwenhoek 51, no. 5-6 (September 1985): 578–79. http://dx.doi.org/10.1007/bf00404564.

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36

Odelson, David A., Jeanette L. Rasmussen, C. Jeffrey Smith, and Francis L. Macrina. "Extrachromosomal systems and gene transmission in anaerobic bacteria." Plasmid 17, no. 2 (March 1987): 87–109. http://dx.doi.org/10.1016/0147-619x(87)90016-3.

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37

Bilynets, Tetyana, Igor Vysekantsev, and Tatyana M. Gurina. "105. Cryopreservation of asporogenic anaerobic bacteria." Cryobiology 53, no. 3 (December 2006): 412. http://dx.doi.org/10.1016/j.cryobiol.2006.10.106.

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38

Yu, Ying-Cui, Yu Tao, and Da-Wen Gao. "Effects of HRT and nitrite/ammonia ratio on anammox discovered in a sequencing batch biofilm reactor." RSC Adv. 4, no. 97 (2014): 54798–804. http://dx.doi.org/10.1039/c4ra06148a.

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There are three key aspects of substrate effect on anaerobic ammonia oxidizing (anammox) bacteria: (1) substrate concentration-based nitrogen loading rate (NLR), (2) hydraulic retention time (HRT)-based NLR and (3) nitrite/ammonia ratio.
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39

Rudolphi, Angelika, Andreas Tschech, and Georg Fuchs. "Anaerobic degradation of cresols by denitrifying bacteria." Archives of Microbiology 155, no. 3 (February 1991): 238–48. http://dx.doi.org/10.1007/bf00252207.

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40

Dangel, Werner, Andreas Tschech, and Georg Fuchs. "Anaerobic metabolism of cyclohexanol by denitrifying bacteria." Archives of Microbiology 150, no. 4 (August 1988): 358–62. http://dx.doi.org/10.1007/bf00408307.

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41

Tsarev, V. N., E. N. Nikolaeva, M. V. Vitovich, M. S. Podporin, and E. V. Ippolitov. "Morphological aspects of microbial biofilm formation on atherosclerotic plaque fragments." Bacteriology 5, no. 2 (2020): 8–17. http://dx.doi.org/10.20953/2500-1027-2020-2-8-17.

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Modern research indicates the presence of living bacteria in atherosclerotic plaques. However, the potential of microbes in the formation of biofilms in arterial plaques has not been studied. Purpose of the study. Identification of biofilms on fragments of arterial vessels with atherosclerotic plaques. Materials and methods. Fragments of atherosclerotic plaques isolated during coronary artery bypass grafting in patients with coronary artery disease were cultured in an exhaustive fluid system under anaerobic conditions in vitro for 1 or 14 days. The presence of biofilms was evaluated using scan
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Cotta, Michael A., Matthew B. Wheeler, and Terence R. Whitehead. "Cyclic AMP in ruminal and other anaerobic bacteria." FEMS Microbiology Letters 124, no. 3 (December 1994): 355–59. http://dx.doi.org/10.1111/j.1574-6968.1994.tb07308.x.

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43

Raffi, Fatemeh, and Carl E. Cerniglia. "An anaerobic nondenaturing gel assay for the detection of azoreductase from anaerobic bacteria." Journal of Microbiological Methods 12, no. 2 (September 1990): 139–48. http://dx.doi.org/10.1016/0167-7012(90)90024-z.

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Jones, C. P., F. B. Carter, W. L. Thomas, C. H. Peete, and W. L. Cherny. "NONSPORE-FORMING ANAEROBIC BACTERIA OF THE VAGINA." Annals of the New York Academy of Sciences 83, no. 2 (December 15, 2006): 259–64. http://dx.doi.org/10.1111/j.1749-6632.1960.tb40899.x.

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Davidova, M. N., N. B. Tarasova, F. K. Mukhitova, and I. U. Karpilova. "Carbon monoxide in metabolism of anaerobic bacteria." Canadian Journal of Microbiology 40, no. 6 (June 1, 1994): 417–25. http://dx.doi.org/10.1139/m94-069.

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46

Unden, G., S. Becker, J. Bongaerts, J. Schirawski, and S. Six. "Oxygen regulated gene expression in facultatively anaerobic bacteria." Antonie van Leeuwenhoek 66, no. 1-3 (1994): 3–22. http://dx.doi.org/10.1007/bf00871629.

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Stams, Alfons J. M. "Metabolic interactions between anaerobic bacteria in methanogenic environments." Antonie van Leeuwenhoek 66, no. 1-3 (1994): 271–94. http://dx.doi.org/10.1007/bf00871644.

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48

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 (June 15, 2021): 6398. http://dx.doi.org/10.3390/ijms22126398.

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Анотація:
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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49

Boquet, Patrice, Patrick Munro, Carla Fiorentini, and Ingo Just. "Toxins from anaerobic bacteria: specificity and molecular mechanisms of action." Current Opinion in Microbiology 1, no. 1 (February 1998): 66–74. http://dx.doi.org/10.1016/s1369-5274(98)80144-6.

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Baumgartner, A., Th Giger, and P. Rohner. "Antibiotic susceptibility of anaerobic bacteria determined by agar dilution." Experientia 42, no. 1 (January 1986): 98. http://dx.doi.org/10.1007/bf01975962.

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