Relevant bibliographies by topics / Lysinibacillus sp

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  1. Journal articles
  2. Dissertations / Theses
  3. Conference papers

Academic literature on the topic 'Lysinibacillus sp'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "Lysinibacillus sp"

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Coorevits, An, Anna E. Dinsdale, Jeroen Heyrman, et al. "Lysinibacillus macroides sp. nov., nom. rev." International Journal of Systematic and Evolutionary Microbiology 62, Pt_5 (2012): 1121–27. http://dx.doi.org/10.1099/ijs.0.027995-0.

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‘Bacillus macroides’ ATCC 12905T ( = DSM 54T = LMG 18474T), isolated in 1947 from cow dung, was not included in the Approved Lists of Bacterial Names and so it lost standing in bacteriological nomenclature. Reinvestigation of the strain, including DNA–DNA relatedness experiments, revealed that ‘Bacillus macroides’ is genomically distinct from its closest relatives Lysinibacillus xylanilyticus , Lysinibacillus boronitolerans and Lysinibacillus fusiformis (as determined by 16S rRNA gene sequence analysis, with pairwise similarity values of 99.2, 98.8 and 98.5 %, respectively, with the type strai
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Kämpfer, Peter, Karin Martin, and Stefanie P. Glaeser. "Lysinibacillus contaminans sp. nov., isolated from surface water." International Journal of Systematic and Evolutionary Microbiology 63, Pt_9 (2013): 3148–53. http://dx.doi.org/10.1099/ijs.0.049593-0.

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A Gram-positive-staining, aerobic, endospore-forming bacterium, isolated as a contamination from an enrichment of enteric bacteria from surface water, was studied using a polyphasic taxonomic approach. 16S rRNA gene sequence similarity comparisons revealed that strain FSt3AT was grouped in the genus Lysinibacillus , most closely related to Lysinibacillus xylanilyticus XDB9T (98.1 %), Lysinibacillus parviboronicapiens BAM-582T and Lysinibacillus sphaericus DSM 28T (both 98.0 %). The 16S rRNA gene sequence similarity to other species of the genus Lysinibacillus was <97.5 %. The allocation to
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Hersanti, Hersanti, Sudarjat Sudarjat, and Andina Damayanti. "Kemampuan Bacillus subtilis dan Lysinibacillus sp. dalam Silika Nano dan Serat Karbon untuk Menginduksi Ketahanan Bawang Merah terhadap Penyakit Bercak Ungu (Alternaria porri (Ell.) Cif)." Agrikultura 30, no. 1 (2019): 8. http://dx.doi.org/10.24198/agrikultura.v30i1.22622.

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ABSTRACTThe ability of Bacillus subtilis and Lysinibacillus sp. singly or mixed, with carbon fiber and nano silica to induce resistance of shallot to purple blotchPurple blotch disease caused by Alternaria porri is one of the major disease on shallot. One of the methods that can be applied to control the disease is the use of antagonistic bacteria. Antagonistic bacteria can be used as a resistance inducer to suppress pathogen development. In this study, Bacillus subtilis and Lysinibacillus sp. were formulated in carbon fiber as a carrier and nano silica 3% as a complementary. This study was co
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Hersanti, Hersanti, Sudarjat Sudarjat, and Andina Damayanti. "Kemampuan Bacillus subtilis dan Lysinibacillus sp. dalam Silika Nano dan Serat Karbon untuk Menginduksi Ketahanan Bawang Merah terhadap Penyakit Bercak Ungu (Alternaria porri (Ell.) Cif)." Agrikultura 30, no. 1 (2019): 8. http://dx.doi.org/10.24198/agrikultura.v30i1.22698.

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ABSTRACTThe ability of Bacillus subtilis and Lysinibacillus sp. singly or mixed, with carbon fiber and nano silica to induce resistance of shallot to purple blotchPurple blotch disease caused by Alternaria porri is one of the major disease on shallot. One of the methods that can be applied to control the disease is the use of antagonistic bacteria. Antagonistic bacteria can be used as a resistance inducer to suppress pathogen development. In this study, Bacillus subtilis and Lysinibacillus sp. were formulated in carbon fiber as a carrier and nano silica 3% as a complementary. This study was co
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Seiler, Herbert, Siegfried Scherer, and Mareike Wenning. "Lysinibacillus meyeri sp. nov., isolated from a medical practice." International Journal of Systematic and Evolutionary Microbiology 63, Pt_4 (2013): 1512–18. http://dx.doi.org/10.1099/ijs.0.039420-0.

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A Gram-positive, oxidase- and catalase-positive, strictly aerobic and motile bacterium, designated WS 4626T, was isolated from a medical practice. Spherical endospores were formed terminally in swollen rods. The genomic DNA G+C content was 37.1 mol%. Cells contained iso-C15 : 0, anteiso-C15 : 0, iso-C17 : 1ω10c, anteiso-C17 : 0 and iso-C17 : 0 as the predominant cellular fatty acids and MK-7 and MK-6 as the major isoprenoid quinones. The major polar lipids were diphosphatidylglycerol, phosphatidylethanolamine and phosphatidylglycerol, the cell-wall peptidoglycan was type A4α, l-Lys-d-Asp and t
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Zhao, Fei, Youzhi Feng, Ruirui Chen, Jianwei Zhang, and Xiangui Lin. "Lysinibacillus alkaliphilus sp. nov., an extremely alkaliphilic bacterium, and emended description of genus Lysinibacillus." International Journal of Systematic and Evolutionary Microbiology 65, Pt_8 (2015): 2426–31. http://dx.doi.org/10.1099/ijs.0.000280.

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A novel aerobic, alkaliphilic, Gram-staining-positive, endospore-forming bacterium, strain OMN17T, was isolated from a typical sandy loam soil under long-term OMN fertilization (half organic manure N plus half mineral N fertilizer) in northern China and was subjected to a polyphasic taxonomic study. The best growth was achieved at 30 °C and pH 8–10 in medium containing 0.5 % (w/v) NaCl. The cell-wall peptidoglycan of strain OMN17T was type A4α; (l -Lys–Gly-d -Asp) and the cell-wall sugars were ribose, traces of galactose and arabinose. The only respiratory quinone found in strain OMN17T was me
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Ren, Yuan, Shao-yi Chen, Hai-yan Yao, and Liu-jie Deng. "Lysinibacillus cresolivorans sp. nov., an m-cresol-degrading bacterium isolated from coking wastewater treatment aerobic sludge." International Journal of Systematic and Evolutionary Microbiology 65, Pt_11 (2015): 4250–55. http://dx.doi.org/10.1099/ijsem.0.000569.

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A Gram-stain-positive, rod-shaped, facultatively anaerobic, endospore-forming bacterium (designated strain SC03T) was isolated from the aerobic treatment sludge of a coking plant (Shaoguan City, China). The optimal pH and temperature for growth were pH 7.0 and 35 °C. On the basis of 16S rRNA gene sequence analysis, strain SC03T was related to the genus Lysinibacillus and the similarity between strain SC03T and the most closely related type strain, Lysinibacillus macroides LMG 18474T, was 94.4 %. The genomic G+C content of the DNA of strain SC03T was 41.2 mol%. Chemotaxonomic data supported the
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Hayat, Rifat, Iftikhar Ahmed, Jayoung Paek, et al. "Lysinibacillus composti sp. nov., isolated from compost." Annals of Microbiology 64, no. 3 (2013): 1081–88. http://dx.doi.org/10.1007/s13213-013-0747-1.

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Lu, Jia-Rui, and Guo-Hong Liu. "Lysinibacillus agricola sp. nov., isolated from soil." Archives of Microbiology 203, no. 7 (2021): 4173–78. http://dx.doi.org/10.1007/s00203-021-02394-4.

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Azmatunnisa, M., K. Rahul, K. V. N. S. Lakshmi, Ch Sasikala, and Ch V. Ramana. "Lysinibacillus acetophenoni sp. nov., a solvent-tolerant bacterium isolated from acetophenone." International Journal of Systematic and Evolutionary Microbiology 65, Pt_6 (2015): 1741–48. http://dx.doi.org/10.1099/ijs.0.000170.

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A Gram-stain-positive, solvent-tolerating, aerobic, rod-shaped bacterium that formed terminal endospores was isolated from the organic solvent acetophenone. The strain, designated JC23T, was oxidase- and catalase-positive. The strain grew in the presence of a wide range of organic solvents with partition coefficients (log p values) between 1 and 4, which are exceptionally toxic to micro-organisms. Based on 16S rRNA gene sequence analysis, strain JC23T was identified as belonging to the genus Lysinibacillus and was most closely related to Lysinibacillus manganicus Mn1-7T (98.5 % similarity), L.
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Dissertations / Theses on the topic "Lysinibacillus sp"

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Chan, K., J. W. Chen, Chien-Yi Chang, W. Yin, and X. Chan. "Draft genome sequence of Lysinibacillus sp. strain A1, isolated from Malaysian tropical soil." 2015. http://hdl.handle.net/10454/15107.

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Yes<br>In this work, we describe the genome of Lysinibacillus sp. strain A1, which was isolated from tropical soil. Analysis of its genome sequence shows the presence of a gene encoding for a putative peptidase responsible for nitrogen compounds.<br>UM High Impact Research Grants (UMMOHE HIR Grant UM C/625/1/HIR/MOHE/CHAN/01, no. A000001- 50001; UM-MOHE HIR Grant UM C/625/1/HIR/MOHE/CHAN/14/1, no. H-50001-A000027)
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Conference papers on the topic "Lysinibacillus sp"

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Reali, V. C., and L. M. Fiuza. "Ecology of Bacillus sp. and Lysinibacillus sp. in rice field soils from Southern Brazil." In MICROBES IN APPLIED RESEARCH - Current Advances and Challenges. WORLD SCIENTIFIC, 2012. http://dx.doi.org/10.1142/9789814405041_0018.

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Rathod, Jagat, and Jiin-Shuh Jean. "UNRAVEL THE WHOLE-GENOME, TRANSCRIPTOME AND ECO-PHYSIOLOGICAL INSIGHTS ON ARSENIC-RESISTANT AND REDOX-ACTIVE GROUNDWATER ISOLATE LYSINIBACILLUS SP. B2A1 INTERACTING WITH ARSENIC-SOURCE MINERAL." In GSA 2020 Connects Online. Geological Society of America, 2020. http://dx.doi.org/10.1130/abs/2020am-354961.

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Journal articles
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