Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Laure Guillotin"'
Autor:
Laure Guillotin, Hyuna Kim, Yasmina Traore, Philippe Moreau, Pierre Lafite, Véronique Coquoin, Sylvie Nuccio, René de Vaumas, Richard Daniellou
Publikováno v:
ACS Omega, Vol 4, Iss 1, Pp 1916-1922 (2019)
Externí odkaz:
https://doaj.org/article/f2c3b5075aaa4732ba26c5e0c9258f48
Autor:
Laure Guillotin, Ludovic Landemarre, Pierre Lafite, Cédric Peyrot, Richard Daniellou, Loïc Lemiègre, Blanka Didak
Publikováno v:
European Journal of Organic Chemistry
European Journal of Organic Chemistry, 2021, 2021 (27), pp.3812-3818. ⟨10.1002/ejoc.202100672⟩
European Journal of Organic Chemistry, Wiley-VCH Verlag, 2021, 2021 (27), pp.3812-3818. ⟨10.1002/ejoc.202100672⟩
European Journal of Organic Chemistry, 2021, 2021 (27), pp.3812-3818. ⟨10.1002/ejoc.202100672⟩
European Journal of Organic Chemistry, Wiley-VCH Verlag, 2021, 2021 (27), pp.3812-3818. ⟨10.1002/ejoc.202100672⟩
International audience; Arbutin, a natural glycoside, is well known as a commercial tyrosinase inhibitor, and thus, to prevent pigmentary disorders of skin. In fact, tyrosinase is involved in the biosynthesis of melanin, the skin main pigment. Howeve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89d31f300e15ffe2520e14f680b560d3
https://hal.science/hal-03331379
https://hal.science/hal-03331379
Autor:
Zeinab Assaf, Salvatore G. Pistorio, Laure Guillotin, Richard Daniellou, Alexei V. Demchenko, Pierre Lafite
Publikováno v:
Catalysts
Catalysts, MDPI, 2019, 9 (10), pp.826. ⟨10.3390/catal9100826⟩
Catalysts, 2019, 9 (10), pp.826. ⟨10.3390/catal9100826⟩
Volume 9
Issue 10
Catalysts, Vol 9, Iss 10, p 826 (2019)
Catalysts, MDPI, 2019, 9 (10), pp.826. ⟨10.3390/catal9100826⟩
Catalysts, 2019, 9 (10), pp.826. ⟨10.3390/catal9100826⟩
Volume 9
Issue 10
Catalysts, Vol 9, Iss 10, p 826 (2019)
International audience; Chemoenzymatic synthesis of glycosides relies on efficient glycosyl donor substrates able to react rapidly and efficiently, yet with increased stability towards chemical or enzymatic hydrolysis. In this context, glycosyl thioi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5799e38ed67b1b2d4bdfb44dcc7ab95
https://hal-univ-orleans.archives-ouvertes.fr/hal-03478291/document
https://hal-univ-orleans.archives-ouvertes.fr/hal-03478291/document
Publikováno v:
Pure and Applied Chemistry
Pure and Applied Chemistry, De Gruyter, 2017, 89 (9), pp.1295-1304. ⟨10.1515/pac-2016-1210⟩
Pure and Applied Chemistry, 2017, 89 (9), pp.1295-1304. ⟨10.1515/pac-2016-1210⟩
Pure and Applied Chemistry, De Gruyter, 2017, 89 (9), pp.1295-1304. ⟨10.1515/pac-2016-1210⟩
Pure and Applied Chemistry, 2017, 89 (9), pp.1295-1304. ⟨10.1515/pac-2016-1210⟩
d-Glycopyranosyl glycerols are common natural products and exhibit strong biological properties, notably as moisturizing agents in cosmetics. Their chemical synthesis remains tedious thus decreasing their potential industrial and economic development
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5f0f664dd6c5561b4e5e36da2f88dfbf
https://hal.archives-ouvertes.fr/hal-01886425
https://hal.archives-ouvertes.fr/hal-01886425
Publikováno v:
Biochimie
Biochimie, Elsevier, 2017, 137, pp.190-196. ⟨10.1016/j.biochi.2017.03.020⟩
Biochimie, 2017, 137, pp.190-196. ⟨10.1016/j.biochi.2017.03.020⟩
Biochimie, Elsevier, 2017, 137, pp.190-196. ⟨10.1016/j.biochi.2017.03.020⟩
Biochimie, 2017, 137, pp.190-196. ⟨10.1016/j.biochi.2017.03.020⟩
Glycoside hydrolases can be turned into thioglycoligase by mutation of the acid/base catalytic carboxylate residue. These mutants have proven valuable to generate S-glycosides, however, few examples in literature have described efficient thioglycolig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f37483378fbb33f1108aaa146e8f753c
https://hal.archives-ouvertes.fr/hal-01608341
https://hal.archives-ouvertes.fr/hal-01608341
Publikováno v:
ChemInform. 45
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a94ba3b60803ad9cb7bba876056f15af
https://doi.org/10.1002/chin.201438245
https://doi.org/10.1002/chin.201438245
Publikováno v:
Biochemistry
Biochemistry, American Chemical Society, 2014, 53 (9), pp.1447-1455. ⟨10.1021/bi400951q⟩
Biochemistry, 2014, 53 (9), pp.1447-1455. ⟨10.1021/bi400951q⟩
Biochemistry, American Chemical Society, 2014, 53 (9), pp.1447-1455. ⟨10.1021/bi400951q⟩
Biochemistry, 2014, 53 (9), pp.1447-1455. ⟨10.1021/bi400951q⟩
International audience; Glycosyl hydrolase (GH) family 29 (CAZy database) consists of retaining $\alpha$-L-fucosidases. We have identified BT2192, a protein from Bacteroides thetaiotaomicron, as the first GH29 representative exhibiting both weak $\al
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8cc2ff86f35d2a6cb3b4d2126a6f2fb8
https://hal-univ-orleans.archives-ouvertes.fr/hal-03478324
https://hal-univ-orleans.archives-ouvertes.fr/hal-03478324
Publikováno v:
Carbohydrate Chemistry
Carbohydrate Chemistry, 40, Royal Society of Chemistry, pp.178-194, 2014, Carbohydrate Chemistry, ⟨10.1039/9781849739986-00178⟩
Carbohydrate Chemistry, 40, Royal Society of Chemistry, pp.178-194, 2014, Carbohydrate Chemistry, ⟨10.1039/9781849739986-00178⟩
Carbohydrates play an important part in a vast array of biological processes and therefore glycomimetics are currently becoming a powerful class of novel therapeutics.1 Amongst them, thioglycosides, in which a sulfur atom has replaced the glycosidic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13281862f1f5cf4a0e50bf7b7c88817f
https://hal-univ-orleans.archives-ouvertes.fr/hal-03478322
https://hal-univ-orleans.archives-ouvertes.fr/hal-03478322
Autor:
Bernard Nicolardot, Virginie Parnaudeau, Gwenaëlle Lashermes, Bruno Mary, Marie-Laure Guillotin, Sabine Houot, Christine Villette, Laurent Thuriès, Thierry Morvan, Antoine Tricaud, Laure Metzger, Rémi Chaussod, Monique Lineres
Publikováno v:
Bioresource Technology
Bioresource Technology, Elsevier, 2010, 101 (1), pp.157-164. ⟨10.1016/j.biortech.2009.08.025⟩
Bioresource Technology, Elsevier, 2010, 101 (1), pp.157-164. 〈10.1016/j.biortech.2009.08.025〉
Bioresource Technology, Elsevier, 2010, 101 (1), pp.157-164. ⟨10.1016/j.biortech.2009.08.025⟩
Bioresource Technology, Elsevier, 2010, 101 (1), pp.157-164. 〈10.1016/j.biortech.2009.08.025〉
Our aim was to develop a typology predicting potential N availability of exogenous organic matters (EOMs) in soil based on their chemical characteristics. A database of 273 EOMs was constructed including analytical data of biochemical fractionation,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6390ac6d712bb96381683a6c8dcde77a
http://agritrop.cirad.fr/550945/
http://agritrop.cirad.fr/550945/
Autor:
Gwenaëlle Lashermes, Sabine Houot, Virginie Parnaudeau, Antoine Tricaud, Bruno Mary, Laurent Thuriès, Christine Villette, Monique Lineres, Thierry Morvan, Bernard Nicolardot, Laure Metzger, Rémi Chaussod, Marie-Laure Guillotin
Publikováno v:
European Journal of Soil Science
European Journal of Soil Science, Wiley, 2009, 60 (2), pp.297-310. ⟨10.1111/j.1365-2389.2008.01110.x⟩
European Journal of Soil Science, Wiley, 2009, 60 (2), pp.297-310. 〈10.1111/j.1365-2389.2008.01110.x〉
European Journal of Soil Science, Wiley, 2009, 60 (2), pp.297-310. ⟨10.1111/j.1365-2389.2008.01110.x⟩
European Journal of Soil Science, Wiley, 2009, 60 (2), pp.297-310. 〈10.1111/j.1365-2389.2008.01110.x〉
An indicator to evaluate the proportion of exogenous organic matter (EOM) remaining in soils over the long-term after application has been developed. A database was constructed with analytical data corresponding to 83 EOMs, including sludges, compost
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ded09aa31097106fbf4e70e85bc80e17
https://hal.archives-ouvertes.fr/hal-01192070
https://hal.archives-ouvertes.fr/hal-01192070