Paenibacillus melissococcoides sp. nov., isolated from a honey bee colony affected by European foulbrood disease

Autor: Florine Ory, Vincent Dietemann, Anne Guisolan, Ueli von Ah, Charlotte Fleuti, Simone Oberhaensli, Jean-Daniel Charrière, Benjamin Dainat

Publikováno v: Ory, Florine; Dietemann, Vincent; Guisolan, Anne; von Ah, Ueli; Fleuti, Charlotte; Oberhaensli, Simone; Charrière, Jean-Daniel; Dainat, Benjamin (2023). Paenibacillus melissococcoides sp. nov., isolated from a honey bee colony affected by European foulbrood disease. International journal of systematic and evolutionary microbiology, 73(4) Microbiology Society 10.1099/ijsem.0.005829
International journal of systematic and evolutionary microbiology, vol. 73, no. 4

A novel, facultatively anaerobic, Gram-stain-positive, motile, endospore-forming bacterium of the genus Paenibacillus , designated strain 2.1T, was isolated from a colony of Apis mellifera affected by European foulbrood disease in Switzerland. The ro

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ef14bd9650bb19f35d0b75155a114e4
https://boris.unibe.ch/182592/1/ijsem005829.pdf

Functionalized Acyclic (l)-Threoninol Nucleic Acid Four-Way Junction with High Stability In Vitro and In Vivo

Autor: Anders Märcher, Vipin Kumar, Veronica L. Andersen, Kassem El‐Chami, Thuy J. D. Nguyen, Mads K. Skaanning, Imke Rudnik‐Jansen, Jesper S. Nielsen, Kenneth A. Howard, Jørgen Kjems, Kurt V. Gothelf

Publikováno v: Märcher, A, Kumar, V, Andersen, V L, El-Chami, K, Nguyen, T J D, Skaanning, M K, Rudnik-Jansen, I, Nielsen, J S, Howard, K A, Kjems, J & Gothelf, K V 2022, ' Functionalized Acyclic (l)-Threoninol Nucleic Acid Four-Way Junction with High Stability In Vitro and In Vivo ', Angewandte Chemie-International Edition, vol. 61, no. 24, 202115275 . https://doi.org/10.1002/anie.202115275

Oligonucleotides are increasingly being used as a programmable connection material to assemble molecules and proteins in well-defined structures. For the application of such assemblies for in vivo diagnostics or therapeutics it is crucial that the ol

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce902a59a08814fbc4843125b4c96ca5
https://pure.au.dk/portal/da/publications/functionalized-acyclic-lthreoninol-nucleic-acid-fourway-junction-with-high-stability-in-vitro-and-in-vivo(2c7f5436-6060-4d45-9a07-53de17409047).html

In Situ Studies of Arylboronic Acids/Esters and R3SiCF3 Reagents: Kinetics, Speciation, and Dysfunction at the Carbanion–Ate Interface

Autor: Guy Lloyd-Jones, Andrew Leach, Andrés García-Domínguez

Publikováno v: García-Domínguez, A, Leach, A G & Lloyd-Jones, G C 2022, ' In Situ Studies of Arylboronic Acids/Esters and R3SiCF3 Reagents: Kinetics, Speciation, and Dysfunction at the Carbanion–Ate Interface ', Accounts of Chemical Research, vol. 55, no. 9, pp. 1324-1336 . https://doi.org/10.1021/acs.accounts.2c00113
García-domínguez, A, Leach, A G & Lloyd-jones, G C 2022, ' In Situ Studies of Arylboronic Acids/Esters and R 3 SiCF 3 Reagents: Kinetics, Speciation, and Dysfunction at the Carbanion–Ate Interface ', Accounts of Chemical Research . https://doi.org/10.1021/acs.accounts.2c00113

ConspectusReagent instability reduces the efficiency of chemical processes, and while much effort is devoted to reaction optimization, less attention is paid to the mechanistic causes of reagent decomposition. Indeed, the response is often to simply

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88cda69a91d8a9697ea16153f3b1347b
https://www.research.manchester.ac.uk/portal/en/publications/in-situ-studies-of-arylboronic-acidsesters-and-r3sicf3-reagents-kinetics-speciation-and-dysfunction-at-the-carbanionate-interface(c7fb67e3-fab3-49c1-bcf5-43c052454344).html

Chemistry, biosynthesis, analysis, chemical and metabolic transformations and pharmacology.

Autor: Popsavin, Velimir¹

Publikováno v: Journal of the Serbian Chemical Society. Jan2008, Vol. 73 Issue 1, p127-129. 3p.

Probing the Lewis Acidity of Boronic Acids through Interactions with Arene Substituents

Autor: Jie Jian, Roel Hammink, Christine J. McKenzie, F. Matthias Bickelhaupt, Jordi Poater, Jasmin Mecinović

Publikováno v: Jian, J, Hammink, R, McKenzie, C J, Bickelhaupt, F M, Poater, J & Mecinović, J 2022, ' Probing the Lewis Acidity of Boronic Acids through Interactions with Arene Substituents ', Chemistry: A European Journal, vol. 28, no. 9, e202104044 . https://doi.org/10.1002/chem.202104044
Jian, J, Hammink, R, McKenzie, C J, Bickelhaupt, F M, Poater, J & Mecinović, J 2022, ' Probing the Lewis Acidity of Boronic Acids through Interactions with Arene Substituents ', Chemistry-A European Journal, vol. 28, no. 9, e202104044, pp. 1-7 . https://doi.org/10.1002/chem.202104044
Chemistry : a European Journal, 28, 1-6
Chemistry-A European Journal, 28(9):e202104044, 1-7. Wiley-VCH Verlag
Chemistry : a European Journal, 28, 9, pp. 1-6

Boronic acids are Lewis acids that exist in equilibrium with boronate forms in aqueous solution. Here we experimentally and computationally investigated the Lewis acidity of 2,6-diarylphenylboronic acids; specially designed phenylboronic acids that p

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f7a7bf082187c00b435f6d9af2016fb
https://lirias.kuleuven.be/handle/20.500.12942/711248