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Showing results for pseudo bacterium rufum. Your search for Pseudobacterium rufum retrieved no results.

Select item 61136281.

Genome-Based Taxonomic Classification of the Phylum Actinobacteria

Imen Nouioui, Lorena Carro, Marina García-López, Jan P. Meier-Kolthoff, Tanja Woyke, Nikos C. Kyrpides, Rüdiger Pukall, Hans-Peter Klenk, Michael Goodfellow, Markus Göker

Front Microbiol. 2018; 9: 2007. Published online 2018 Aug 22. doi: 10.3389/fmicb.2018.02007

PMCID:: PMC6113628

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Phylogenomics and Comparative Genomic Studies Robustly Support Division of the Genus Mycobacterium into an Emended Genus Mycobacterium and Four Novel Genera

Radhey S. Gupta, Brian Lo, Jeen Son

Front Microbiol. 2018; 9: 67. Published online 2018 Feb 13. doi: 10.3389/fmicb.2018.00067

Correction in:: Front Microbiol. 2019; 10: 714.

PMCID:: PMC5819568

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Select item 52093073.

Microbial communities in pyrene amended soil–compost mixture and fertilized soil

Iris K. U. Adam, Márcia Duarte, Jananan Pathmanathan, Anja Miltner, Thomas Brüls, Matthias Kästner

AMB Express. 2017; 7: 7. Published online 2017 Jan 3. doi: 10.1186/s13568-016-0306-9

PMCID:: PMC5209307

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Select item 41876424.

Microbiological Features and Clinical Relevance of New Species of the Genus Mycobacterium

Enrico Tortoli

Clin Microbiol Rev. 2014 Oct; 27(4): 727–752. doi: 10.1128/CMR.00035-14

PMCID:: PMC4187642

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Select item 99480035.

Fungal diversity notes 1512–1610: taxonomic and phylogenetic contributions on genera and species of fungal taxa

Ruvishika S. Jayawardena, Kevin D. Hyde, Song Wang, Ya-Ru Sun, Nakarin Suwannarach, Phongeun Sysouphanthong, Mohamed A. Abdel-Wahab, Faten A. Abdel-Aziz, Pranami D. Abeywickrama, Vanessa P. Abreu, Alireza Armand, André Aptroot, Dan-Feng Bao, Dominik Begerow, Jean-Michel Bellanger, Jadson D. P. Bezerra, Digvijayini Bundhun, Mark S. Calabon, Ting Cao, Taimy Cantillo, João L. V. R. Carvalho, Napalai Chaiwan, Che-Chih Chen, Régis Courtecuisse, Bao-Kai Cui, Ulrike Damm, Cvetomir M. Denchev, Teodor T. Denchev, Chun Y. Deng, Bandarupalli Devadatha, Nimali I. de Silva, Lidiane A. dos Santos, Nawal K. Dubey, Sylvain Dumez, Himashi S. Ferdinandez, André L. Firmino, Yusufjon Gafforov, Achala J. Gajanayake, Deecksha Gomdola, Sugantha Gunaseelan, Shucheng-He, Zin H. Htet, Malarvizhi Kaliyaperumal, Martin Kemler, Kezhocuyi Kezo, Nuwan D. Kularathnage, Marco Leonardi, Ji-Peng Li, Chunfang Liao, Shun Liu, Michael Loizides, Thatsanee Luangharn, Jian Ma, Hugo Madrid, S. Mahadevakumar, Sajeewa S. N. Maharachchikumbura, Dimuthu S. Manamgoda, María P. Martín, Niranjan Mekala, Pierre-Arthur Moreau, Yan-Hong Mu, Pasouvang Pahoua, Dhandevi Pem, Olinto L. Pereira, Wiphawanee Phonrob, Chayanard Phukhamsakda, Mubashar Raza, Guang-Cong Ren, Andrea C. Rinaldi, Walter Rossi, Binu C. Samarakoon, Milan C. Samarakoon, Vemuri V. Sarma, Indunil C. Senanayake, Archana Singh, Maria F. Souza, Cristina M. Souza-Motta, Adriano A. Spielmann, Wenxin Su, Xia Tang, XingGuo Tian, Kasun M. Thambugala, Naritsada Thongklang, Danushka S. Tennakoon, Nopparat Wannathes, DingPeng Wei, Stéphane Welti, Subodini N. Wijesinghe, Hongde Yang, Yunhui Yang, Hai-Sheng Yuan, Huang Zhang, Jingyi Zhang, Abhaya Balasuriya, Chitrabhanu S. Bhunjun, Timur S. Bulgakov, Lei Cai, Erio Camporesi, Putarak Chomnunti, Y. S. Deepika, Mingkwan Doilom, Wei-Jun Duan, Shi-Ling Han, Naruemon Huanraluek, E. B. Gareth Jones, N. Lakshmidevi, Yu Li, Saisamorn Lumyong, Zong-Long Luo, Surapong Khuna, Jaturong Kumla, Ishara S. Manawasinghe, Ausana Mapook, Wilawan Punyaboon, Saowaluck Tibpromma, Yong-Zhong Lu, JiYe Yan, Yong Wang

Fungal Divers. 2022; 117(1): 1–272. Published online 2023 Feb 23. doi: 10.1007/s13225-022-00513-0

PMCID:: PMC9948003

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Select item 36075486.

Multiple degradation pathways of phenanthrene by Stenotrophomonas maltophilia C6

Shumei Gao, Jong-Su Seo, Jun Wang, Young-Soo Keum, Jianqiang Li, Qing X. Li

Int Biodeterior Biodegradation. Author manuscript; available in PMC 2014 Apr 1.

Published in final edited form as: Int Biodeterior Biodegradation. 2013 Apr 1; 79: 98–104. Published online 2013 Mar 6. doi: 10.1016/j.ibiod.2013.01.012

PMCID:: PMC3607548

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Select item 61253577.

Global Environmental Nontuberculous Mycobacteria and Their Contemporaneous Man-Made and Natural Niches

Jennifer R. Honda, Ravleen Virdi, Edward D. Chan

Front Microbiol. 2018; 9: 2029. Published online 2018 Aug 30. doi: 10.3389/fmicb.2018.02029

PMCID:: PMC6125357

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Select item 108794878.

Cultivable fungal diversity in two karstic caves in Italy: under-investigated habitats as source of putative novel taxa

A. Poli, A. Zanellati, E. Piano, F. Biagioli, C. Coleine, G. Nicolosi, L. Selbmann, M. Isaia, V. Prigione, G. C. Varese

Sci Rep. 2024; 14: 4164. Published online 2024 Feb 20. doi: 10.1038/s41598-024-54548-1

PMCID:: PMC10879487

Article PDF–2.5M

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PMC Images search for Pseudobacterium rufum

Fig. 3.

Plots depicting the functionality of aposporous embryo sacs (AES) and the capacity for apomixis in different diploid genotypes of P. rufum. Percentages of seeds derived from functional aposporous embryo sacs after: (A) conspecific interploidy pollination with tetraploid P. rufum; (B) induced self-pollination with mentor pollen of tetraploid P. urvillei. Circle areas are proportional to the number of caryopses analysed in each genotype.

Analysis of variation for apomictic reproduction in diploid Paspalum rufum

Ann Bot. 2014 Jun;113(7):1211-1218.
Figure 5

Linkage map of the diploid (2n = 2x) maternal genotype of P. rufum (R6#45). Markers and distances in cM (Kosambi) are indicated on the right and left, respectively. Each co-segregation group includes SDAF and BSDF (starting with an X) markers in coupling and repulsion-phase (-).

Environmental and Genetic Factors Affecting Apospory Expressivity in Diploid Paspalum rufum

Plants (Basel). 2021 Oct;10(10):2100.
Fig. 4.

Cytoembryological analysis of diploid plants of Paspalum rufum. (A) Ovule with a single meiotic embryo sac from plant R6#45. (B) Ovule bearing a meiotic sac plus an aposporous-like embryo sac of plant R5#49. MES, meiotic embryo sac; AES, aposporous-like embryo sac; p, polar nuclei; e, egg cell; s, synergids; a, antipodals. Scale bars = 150 μm.

Analysis of variation for apomictic reproduction in diploid Paspalum rufum

Ann Bot. 2014 Jun;113(7):1211-1218.
Fig. 2

A scanning electron micrograph of M. rufum JS14^T. The image was taken using a Field Emission Scanning Electron Microscope (SU8220; Hitachi, Japan) at an operating voltage of 10.0 kV. The scale bar represents 5.0 μm

Draft genome sequence of Mycobacterium rufum JS14T, a polycyclic-aromatic-hydrocarbon-degrading bacterium from petroleum-contaminated soil in Hawaii

Stand Genomic Sci. 2016;11:47.