Journal articles on the topic 'Actinomycetales'

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1

Safo-Sampah, Stephen, and John G. Torrey. "Polysaccharide-hydrolyzing enzymes ofFrankia (Actinomycetales)." Plant and Soil 112, no. 1 (November 1988): 89–97. http://dx.doi.org/10.1007/bf02181757.

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2

Stanford, John L. "Interview: Investigating immunomodulators among the Actinomycetales." Immunotherapy 5, no. 5 (May 2013): 449–52. http://dx.doi.org/10.2217/imt.13.27.

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3

Kalakoutskii, L. V. "Ray Fungi and Related Organisms (Actinomycetales)." Microbiology 73, no. 5 (September 2004): 523–30. http://dx.doi.org/10.1023/b:mici.0000044243.92023.1f.

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4

LECHEVALIER, M. P. "Taxonomy of the Genus Frankia (Actinomycetales)." International Journal of Systematic Bacteriology 44, no. 1 (January 1, 1994): 1–8. http://dx.doi.org/10.1099/00207713-44-1-1.

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5

HOLTZ, HOWARD A. "Actinomycetales Infection in the Acquired Immunodeficiency Syndrome." Annals of Internal Medicine 102, no. 2 (February 1, 1985): 203. http://dx.doi.org/10.7326/0003-4819-102-2-203.

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6

Hasegawa, Toru. "Actinokineospora: A new genus of the Actinomycetales." Actinomycetologica 2, no. 1 (1988): 31–45. http://dx.doi.org/10.3209/saj.2_31.

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7

Kirby, Ralph. "Chromosome diversity and similarity within the Actinomycetales." FEMS Microbiology Letters 319, no. 1 (March 29, 2011): 1–10. http://dx.doi.org/10.1111/j.1574-6968.2011.02242.x.

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8

Hugonnet, Jean-Emmanuel, Nabila Haddache, Carole Veckerlé, Lionel Dubost, Arul Marie, Noriyasu Shikura, Jean-Luc Mainardi, Louis B. Rice, and Michel Arthur. "Peptidoglycan Cross-Linking in Glycopeptide-Resistant Actinomycetales." Antimicrobial Agents and Chemotherapy 58, no. 3 (January 6, 2014): 1749–56. http://dx.doi.org/10.1128/aac.02329-13.

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ABSTRACTSynthesis of peptidoglycan precursors ending ind-lactate (d-Lac) is thought to be responsible for glycopeptide resistance in members of the orderActinomycetalesthat produce these drugs and in related soil bacteria. More recently, the peptidoglycan of several members of the orderActinomycetaleswas shown to be cross-linked byl,d-transpeptidases that use tetrapeptide acyl donors devoid of the target of glycopeptides. To evaluate the contribution of these resistance mechanisms, we have determined the peptidoglycan structure ofStreptomyces coelicolorA(3)2, which harbors avanHAXgene cluster for the production of precursors ending ind-Lac, andNonomuraeasp. strain ATCC 39727, which is devoid ofvanHAXand produces the glycopeptide A40296. Vancomycin retained residual activity againstS. coelicolorA(3)2 despite efficient incorporation ofd-Lac into cytoplasmic precursors. This was due to ad,d-transpeptidase-catalyzed reaction that generated a stem pentapeptide recognized by glycopeptides by the exchange ofd-Lac ford-Ala and Gly. The contribution ofl,d-transpeptidases to resistance was limited by the supply of tetrapeptide acyl donors, which are essential for the formation of peptidoglycan cross-links by these enzymes. In the absence of a cytoplasmic metallo-d,d-carboxypeptidase, the tetrapeptide substrate was generated by hydrolysis of the C-terminald-Lac residue of the stem pentadepsipeptide in the periplasm in competition with the exchange reaction catalyzed byd,d-transpeptidases. InNonomuraeasp. strain ATCC 39727, the contribution ofl,d-transpeptidases to glycopeptide resistance was limited by the incomplete conversion of pentapeptides into tetrapeptides despite the production of a cytoplasmic metallo-d,d-carboxypeptidase. Since the level of drug production exceeds the level of resistance, we propose thatl,d-transpeptidases merely act as a tolerance mechanism in this bacterium.
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9

Meyertons, Janise L., Bruce C. Tilley, Mary P. Lechevalier, and Hubert A. Lechevalier. "Actinophages and restriction enzymes fromMicromonospora species (Actinomycetales)." Journal of Industrial Microbiology 2, no. 5 (December 1987): 293–303. http://dx.doi.org/10.1007/bf01569432.

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10

KOBAYASHI, Kenzoh, Masahiro YOSHIDA, Takenori NAKAYAMA, and Seiji KOGA. "Root tumor of melon caused by Actinomycetales." Japanese Journal of Phytopathology 53, no. 4 (1987): 562–65. http://dx.doi.org/10.3186/jjphytopath.53.562.

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11

MIYADOH, S., H. TOHYAMA, S. AMANO, T. SHOMURA, and T. NIIDA. "Microbispora viridis, a New Species of Actinomycetales." International Journal of Systematic Bacteriology 35, no. 3 (July 1, 1985): 281–84. http://dx.doi.org/10.1099/00207713-35-3-281.

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12

LABEDA, D. P., R. T. TESTA, M. P. LECHEVALIER, and H. A. LECHEVALIER. "Glycomyces, a New Genus of the Actinomycetales." International Journal of Systematic Bacteriology 35, no. 4 (October 1, 1985): 417–21. http://dx.doi.org/10.1099/00207713-35-4-417.

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13

Asano, K., and I. Kawamoto. "Catellatospora, a New Genus of the Actinomycetales." International Journal of Systematic Bacteriology 36, no. 4 (October 1, 1986): 512–17. http://dx.doi.org/10.1099/00207713-36-4-512.

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14

Hund, Hilda-K., Brigitte Keller, and Franz Lingens. "Phenylalanine and Tyrosine Biosynthesis in Sporeforming Members of the Order Actinomycetales." Zeitschrift für Naturforschung C 42, no. 4 (April 1, 1987): 387–93. http://dx.doi.org/10.1515/znc-1987-0410.

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Abstract The enzymes of the terminal steps of phenylalanine and tyrosine biosynthesis, chorismate mutase, prephenate dehydratase, arogenate dehydratase, prephenate dehydrogenase and aroge­ nate dehydrogenase were studied in 13 sporeforming members of the order Actinomycetales. In these organisms tyrosine is synthesized exclusively via arogenate, phenylalanine, however, via phenylpyruvate. The regulation pattern of the corresponding enzymes was determined: No feed­ back inhibition of arogenate dehydrogenase by L-phenylalanine and ʟ-tyrosine was observed. Chorismate mutase was found to be inhibited in all organisms by ʟ-tyrosine and in most organisms by ʟ-tryptophan. ʟ-Phenylalanine was shown to inhibit prephenate dehydratase in the majority of bacteria tested and ʟ-tyrosine activated this enzyme in most cases. The elution profiles for the phenylalanine and tyrosine biosynthetic enzymes were studied in three members of the order Actinomycetales by anion exchange chromatography on DEAE-cellulose.
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15

Bruns, Alke, Ulrich Nübel, Heribert Cypionka, and Jörg Overmann. "Effect of Signal Compounds and Incubation Conditions on the Culturability of Freshwater Bacterioplankton." Applied and Environmental Microbiology 69, no. 4 (April 2003): 1980–89. http://dx.doi.org/10.1128/aem.69.4.1980-1989.2003.

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ABSTRACT The effect of signal compounds and of different incubation conditions on the culturability (i.e., the fraction of all cells capable of growth) of natural bacterioplankton from the eutrophic lake Zwischenahner Meer was investigated over a period of 20 months. Numbers of growing cells were determined by the most-probable-number technique in liquid media containing low concentrations (10 μM) of the signal compounds N-(oxohexanoyl)-dl-homoserine lactone, N-(butyryl)-dl-homoserine lactone, cyclic AMP (cAMP), or ATP. cAMP was the most effective signal compound, leading to significantly increased cultivation efficiencies of up to 10% of the total bacterial counts. Microautoradiography with [2,8-3H]cAMP, combined with fluorescence in situ hybridization, demonstrated that cAMP was taken up by 18% of all cells. The bacterial cAMP uptake systems had a very low Km value of ≤1 nM. Analysis of the cultured bacteria by 16S rRNA gene fingerprinting showed that different bacterial phylotypes were recovered in the presence and in the absence of cAMP. Consequently, the addition of cAMP caused a stimulation of otherwise nonculturable bacteria. Phylogenetically different bacteria were also recovered at different temperatures and oxygen partial pressures. Throughout the study period, mainly members of the β-subclass of the Proteobacteria were cultivated. In addition, some members of the Actinomycetales were enriched. Quantification by culture-independent fluorescence in situ hybridization demonstrated that β-Proteobacteria and Actinomycetales also dominated the natural bacterioplankton assemblage. Sequence comparison revealed that two members of the Actinomycetales which reached high numbers in the natural bacterioplankton assemblage could actually be enriched by our cultivation approach.
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16

Miyadoh, S., S. Amano, H. Tohyama, and T. Shomura. "Actinomadura atramentaria, a New Species of the Actinomycetales." International Journal of Systematic Bacteriology 37, no. 4 (October 1, 1987): 342–46. http://dx.doi.org/10.1099/00207713-37-4-342.

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17

Jiang, C., L. Xu, Y. R. Yang, G. Y. Guo, J. Ma, and Y. Liu. "Actinobispora, a New Genus of the Order Actinomycetales." International Journal of Systematic Bacteriology 41, no. 4 (October 1, 1991): 526–28. http://dx.doi.org/10.1099/00207713-41-4-526.

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18

Beyazova, M., and M. P. Lechevalier. "Low-Frequency Restriction Fragment Analysis of Frankia Strains (Actinomycetales." International Journal of Systematic Bacteriology 42, no. 3 (July 1, 1992): 422–33. http://dx.doi.org/10.1099/00207713-42-3-422.

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19

Luo, Yan, Zuo Ming Xie, Yi Fang Zhou, and Yan Xin Wang. "Bacterial Diversity in the High Arsenic Groundwater Systems of Jianghan Plain and Datong Basin by 16S rDNA Clone Library." Advanced Materials Research 726-731 (August 2013): 35–38. http://dx.doi.org/10.4028/www.scientific.net/amr.726-731.35.

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To compare the difference bacterial diversity between Jianghan plain and Datong basin. The high arsenic sediment samples in this study were collected from different depths of borehole. The bacterial diversity in high arsenic aquifer sediments was studied by 16S rDNA clone library. The dominant bacterial community included Burkholderiales, Pseudomonadales, and Enterobacteriales in Jianghan plain, and Burkholderiales,Enterobacteriales and Actinomycetales in Datong basin.
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20

Ablanedo-Terrazas, Yuria, Christopher E. Ormsby, and Gustavo Reyes-Terán. "Palatal Actinomycosis and Kaposi Sarcoma in an HIV-Infected Subject with DisseminatedMycobacterium avium-intracellulareInfection." Case Reports in Medicine 2012 (2012): 1–3. http://dx.doi.org/10.1155/2012/679728.

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ActinomycesandMycobacterium avium-intracellulareare facultative intracellular organisms, members of the bacterial order actinomycetales. AlthoughActinomycescan behave as copathogen when anatomic barriers are compromised, its coinfection withMycobacterium avium-intracellularehas not previously been reported. We present the first reported case of palatal actinomycosis co-infection with disseminated MAC, in an HIV-infected subject with Kaposi sarcoma and diabetes. We discuss the pathogenesis of the complex condition of this subject.
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21

Marro, Alicia, Mónica Pirles, Laura Schiaffino, Liliana Bin, Héctor Dávila, Oscar A. Bottasso, Graham McIntyre, Paul R. Ripley, Cynthia A. Stanford, and John L. Stanford. "Successful immunotherapy of canine flea allergy with injected Actinomycetales preparations." Immunotherapy 3, no. 8 (August 2011): 971–78. http://dx.doi.org/10.2217/imt.11.93.

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22

TAKAHASHI, YOKO, YOSHITAKE TANAKA, YUZURU IWAI, and SATOSHI OMURA. "Promicromonospora sukumoe sp. nov., a new species of the Actinomycetales." Journal of General and Applied Microbiology 33, no. 6 (1987): 507–19. http://dx.doi.org/10.2323/jgam.33.507.

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23

Pridham, Thomas G. "Physiological characteristics and the species concept in Actinomycetales , (Volume 18)." Journal of Industrial Microbiology and Biotechnology 22, no. 4-5 (April 1, 1999): 361–71. http://dx.doi.org/10.1038/sj.jim.2900649.

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24

Labeda, D. P., R. T. Testa, M. P. Lechevalier, and H. A. Lechevalier. "Saccharothrix: a New Genus of the Actinomycetales Related to Nocardiopsis." International Journal of Systematic Bacteriology 35, no. 1 (January 1, 1985): 126. http://dx.doi.org/10.1099/00207713-35-1-126b.

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25

IINUMA, S., A. YOKOTA, T. HASEGAWA, and T. KANAMARU. "Actinocorallia gen. nov., a New Genus of the Order Actinomycetales." International Journal of Systematic Bacteriology 44, no. 2 (April 1, 1994): 230–34. http://dx.doi.org/10.1099/00207713-44-2-230.

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26

YASSIN, A. F., F. A. RAINEY, H. BRZEZINKA, K. D. JAHNKE, H. WEISSBRODT, H. BUDZIKIEWICZ, E. STACKEBRANDT, and K. P. SCHAAL. "Lentzea gen. nov., a New Genus of the Order Actinomycetales." International Journal of Systematic Bacteriology 45, no. 2 (April 1, 1995): 357–63. http://dx.doi.org/10.1099/00207713-45-2-357.

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27

Lee, S. D., S. O. Kang, and Y. C. Hah. "Hongia gen. nov., a new genus of the order Actinomycetales." International Journal of Systematic and Evolutionary Microbiology 50, no. 1 (January 1, 2000): 191–99. http://dx.doi.org/10.1099/00207713-50-1-191.

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28

Tamura, T., S. Suzuki, and K. Hatano. "Acrocarpospora gen. nov., a new genus of the order Actinomycetales." International Journal of Systematic and Evolutionary Microbiology 50, no. 3 (May 1, 2000): 1163–71. http://dx.doi.org/10.1099/00207713-50-3-1163.

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29

Kinde, Hailu, Richard L. Walker, Virginia A. Skinner, Barbara M. Daft, and Roberta L. Hughes. "Actinomycetales infections in slender-horned gazelles: Six cases (1987-1989)." Journal of the American Veterinary Medical Association 200, no. 11 (June 1, 1992): 1719–22. http://dx.doi.org/10.2460/javma.1992.200.11.1719.

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Summary Disseminated Actinomycetales infections were diagnosed in 6 slender-horned gazelles at a zoologic park over a 17-month period. Nocardia and Mycobacterium spp were isolated. Possible predisposing causes leading to infection were investigated. Environmental contamination where the gazelles were housed was not high, and other breeds of gazelles at the park did not become infected, indicating that environmental exposure was not the sole factor involved. Information gathered from questionnaires sent to other zoologic parks and personnel communications indicated that this was not an isolated incident. Investigation into the genetic lineage of the gazelles revealed substantial inbreeding in prior generations. These findings suggested inbreeding may have been an important predisposing factor leading to infection. Careful scrutiny to ensure maximal heterozygosity of future breedings is warranted.
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30

Chazen, Geoffrey. "Nocardia." Infection Control 8, no. 6 (June 1987): 260–63. http://dx.doi.org/10.1017/s0195941700066169.

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In 1888, Nocard isolated the microorganism responsible for a disease in cattle known as farcy. Eppinger, in 1890, isolated the same pathogen from man. With time, this aerobic gram-positive, partially acid-fast, branching rod became known as Nocardia. Whether Nocardia is a bacterium or fungus was debated for some years. Nocardia has now been classified according to Bergey's system as a bacterium in group 17, order 1: Actinomycetales, family VI: Nocardiaceae.
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31

Desouky, Said E., Mohammed Abu-Elghait, Eman A. Fayed, Samy Selim, Basit Yousuf, Yasuhiro Igarashi, Basel A. Abdel-Wahab, Amnah Mohammed Alsuhaibani, Kenji Sonomoto, and Jiro Nakayama. "Secondary Metabolites of Actinomycetales as Potent Quorum Sensing Inhibitors Targeting Gram-Positive Pathogens: In Vitro and In Silico Study." Metabolites 12, no. 3 (March 15, 2022): 246. http://dx.doi.org/10.3390/metabo12030246.

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Anti-virulence agents are non-bacteriostatic and non-bactericidal emerging therapeutic options which hamper the production of virulence factors in pathogenic flora. In Staphylococcus aureus and Enterococcus faecalis, regulation of virulence genes’ expression occurs through the cyclic peptide-mediated accessory gene regulator (agr) and its ortholog fsr quorum sensing systems, respectively. In the present study, we screened a set of 54 actinomycetales secondary metabolites as novel anti-virulence compounds targeting quorum sensing system of the Gram-positive bacteria. The results indicated that four compounds, Phenalinolactones A–D, BU–4664LMe, 4,5-dehydrogeldamycin, and Questinomycin A, potentially inhibit the agr quorum sensing system and hemolytic activity of S. aureus. On the other hand, Decatromicin A and B, Okilactomycin, Rishirilide A, Abyssomicin I, and Rebeccamycin selectively blocked the fsr quorum sensing system and the gelatinase production in E. faecalis at sub-lethal concentrations. Interestingly, Synerazol uniquely showed the capability to inhibit both fsr and agr quorum sensing systems. Further, in silico molecular docking studies were performed which provided closer insights into the mode of action of these compounds and proposed that the inhibitory activity of these compounds could be attributed to their potential ability to bind to the ATP-active site of S. aureus AgrA. Taken together, our study highlights the potential of actinomycetales secondary metabolites with diverse structures as anti-virulence quorum sensing inhibitors.
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32

Yamada, Yuuki, Mamoru Komatsu, and Haruo Ikeda. "Chemical diversity of labdane-type bicyclic diterpene biosynthesis in Actinomycetales microorganisms." Journal of Antibiotics 69, no. 7 (January 27, 2016): 515–23. http://dx.doi.org/10.1038/ja.2015.147.

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33

SHEARER, M. C., P. M. COLMAN, R. M. FERRIN, L. J. NISBET, and C. H. NASH. "New Genus of the Actinomycetales: Kibdelosporangium aridum gen. nov., sp. nov." International Journal of Systematic Bacteriology 36, no. 1 (January 1, 1986): 47–54. http://dx.doi.org/10.1099/00207713-36-1-47.

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34

Sharp, Jonathan O., Christopher M. Sales, and Lisa Alvarez-Cohen. "Functional characterization of propane-enhanced N-nitrosodimethylamine degradation by two actinomycetales." Biotechnology and Bioengineering 107, no. 6 (November 4, 2010): 924–32. http://dx.doi.org/10.1002/bit.22899.

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35

Wachowska, U., and B. Majchrzak. "Microorganisms colonising the rhizosphere of winter wheat protected with Impact Super 347 SC fungicide and Bion 50 WG plant resistance stimulator." Plant Protection Science 38, SI 2 - 6th Conf EFPP 2002 (December 31, 2017): 442–45. http://dx.doi.org/10.17221/10518-pps.

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In a field experiment, the effect of plant protection agents on fungal colonies colonising the rhizoplane and the rhizosphere of Elena winter wheat was determined. Impact super 347 SC (flutriafol and chlorotalonil) limited the number of fungi representing Trichoderma, promoted the growth of both fungi from the Fusarium gene and bacteria of Pseudomonas in addition to tricalcium phosphate hydrolysing bacteria. The plant resistance stimulator Bion 50 WG (acybenzolar-s-methyl) strongly reduced the population of Actinomycetales. Bacteria representing Azotobacter did not respond to the applied agents.
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36

Kurtböke, Ipek. "From Actinomycin onwards: Actinomycete success stories." Microbiology Australia 33, no. 3 (2012): 108. http://dx.doi.org/10.1071/ma12108.

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The discovery, development and exploitation of antibiotics was one of the most significant advances in medicine in the 20th century. In a golden era lasting from the 1940s to the late 1960s, antibiotic research provided mankind with a wide range of structurally diverse and effective agents for the treatment of microbial infections. Since then, the members of the order Actinomycetales, most notably the genus Streptomyces have proved to be a particularly rich source of antibiotics (Table 1) with extensive therapeutic applications, possibly because of the extra-large DNA complement of these bacteria.
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37

Davila, Hector, Griselda Didoli, Oscar Bottasso, and John Stanford. "Maternal immunization with actinomycetales immunomodulators reduces parasitemias in offspring challenged withTrypanosoma cruzi." Immunotherapy 3, no. 4 (April 2011): 577–83. http://dx.doi.org/10.2217/imt.11.14.

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38

Phelps, T. J., K. Malachowsky, R. M. Schram, and D. C. White. "Aerobic mineralization of vinyl chloride by a bacterium of the order Actinomycetales." Applied and Environmental Microbiology 57, no. 4 (1991): 1252–54. http://dx.doi.org/10.1128/aem.57.4.1252-1254.1991.

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39

Rainey, Frederick A., Peter Schumann, Helmut Prauser, Rosemary Toalster, and Erko Stackebrandt. "Sporichthya polymorpha represents a novel line of descent within the order Actinomycetales." FEMS Microbiology Letters 109, no. 2-3 (May 1993): 263–67. http://dx.doi.org/10.1111/j.1574-6968.1993.tb06178.x.

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40

Cheng, Xing C., Paul R. Jensen, and William Fenical. "Arenaric Acid, a New Pentacyclic Polyether Produced by a Marine Bacterium (Actinomycetales)." Journal of Natural Products 62, no. 4 (April 1999): 605–7. http://dx.doi.org/10.1021/np9801357.

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41

Mokni-Tlili, Sonia, Inès Mehri, Manel Ghorbel, Wafa Hassen, Abdennaceur Hassen, Naceur Jedidi, and Helmi Hamdi. "Community-level genetic profiles of actinomycetales in long-term biowaste-amended soils." Archives of Microbiology 202, no. 10 (July 20, 2020): 2607–17. http://dx.doi.org/10.1007/s00203-020-01935-7.

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42

Barry, Daniel P., and Blaine L. Beaman. "Modulation of eukaryotic cell apoptosis by members of the bacterial order Actinomycetales." Apoptosis 11, no. 10 (July 15, 2006): 1695–707. http://dx.doi.org/10.1007/s10495-006-9236-3.

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43

KAMIUNTEN, Hiroshi, and Nobuo MORI. "Studies on the isolation and inoculation of Actinomycetales causing root tumor of melon." Kyushu Plant Protection Research 34 (1988): 38–40. http://dx.doi.org/10.4241/kyubyochu.34.38.

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44

Lapalikar, Gauri V., Matthew C. Taylor, Andrew C. Warden, Colin Scott, Robyn J. Russell, and John G. Oakeshott. "F420H2-Dependent Degradation of Aflatoxin and other Furanocoumarins Is Widespread throughout the Actinomycetales." PLoS ONE 7, no. 2 (February 27, 2012): e30114. http://dx.doi.org/10.1371/journal.pone.0030114.

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45

Hardt, Ingo H., Paul R. Jensen, and William Fenical. "Neomarinone, and new cytotoxic marinone derivatives, produced by a marine filamentous bacterium (actinomycetales)." Tetrahedron Letters 41, no. 13 (March 2000): 2073–76. http://dx.doi.org/10.1016/s0040-4039(00)00117-9.

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46

Singh, Pratik Raj, Harsha Bajaj, Roland Benz, Mathias Winterhalter, and Kozhinjampara R. Mahendran. "Transport across the outer membrane porin of mycolic acid containing actinomycetales: Nocardia farcinica." Biochimica et Biophysica Acta (BBA) - Biomembranes 1848, no. 2 (February 2015): 654–61. http://dx.doi.org/10.1016/j.bbamem.2014.11.020.

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47

Asano, K., and I. Kawamoto. "Catellatospora citrea subsp. methionotrophica subsp. nov., a Methionine-Deficient Auxotroph of the Actinomycetales." International Journal of Systematic Bacteriology 38, no. 3 (July 1, 1988): 326–27. http://dx.doi.org/10.1099/00207713-38-3-326.

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48

Salar-Vidal, Llanos, Marta Martín-García, Alicia Macías-Valcayo, Ana Ponz, and Jaime Esteban. "Epidemiology and in vitro antimicrobial susceptibility of aerobic Actinomycetales in a clinical setting." Enfermedades infecciosas y microbiologia clinica (English ed.) 40, no. 10 (December 2022): 562–67. http://dx.doi.org/10.1016/j.eimce.2021.02.014.

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49

Breton, Gérard. "The Actinomycetales of the Sparnacian amber from Corbières (Aude, France): taphonomy and diversity." Annales de la Société Géologique du Nord, no. 17 (December 1, 2010): 3–22. http://dx.doi.org/10.54563/asgn/1207.

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Les sédiments sparnaciens de Douzens (Aude, France) ont livré de nombreux fragments d’ambre. L’examen au microscope optique de cet ambre a révélé la présence d’actinomycètes nombreux et variés. Deux genres nouveaux, Thermomonosporopsis et Thermomonosporites et huit espèces nouvelles, Thermomonosporopsis waggoneri, T. tenuis, Thermomonospora corbarica, Thermomonosporites arcuatus, Nocardia ? cousini, N. ? crispa, Actinoplanes ? girardi, et Streptomyces vizcainoi sont décrits sur la base de caractères morphologiques, de la préservation de structures reproductrices (spores, sporanges, rameaux sporifères), de la dualité éventuelle des mycéliums et de structures de multiplication (fragmentation du mycélium). A côté du piégeage dans la résine, un processus taphonomique original est décrit : au moins une espèce a été capable de coloniser la surface de la résine et de croître dans cette résine.
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Kirby, Ralph, Paul Herron, and Paul Hoskisson. "Analysis of developmental gene conservation in the Actinomycetales using DNA/DNA microarray comparisons." Antonie van Leeuwenhoek 99, no. 2 (June 30, 2010): 159–77. http://dx.doi.org/10.1007/s10482-010-9473-x.

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