Synthesis of 1,2-phenylenediamine capturing molecule for the detection of diacetyl

Autor: Lucia Marri, Anita M. Jansson, Caspar E. Christensen, Ole Hindsgaul

Publikováno v: Data in Brief, Vol 15, Iss , Pp 483-490 (2017)

Here we describe the design of 1,2-phenylenediamine capturing molecule and the synthesis steps necessary for its preparation. The designed 1,2-phenylenediamine derivative is able to capture diacetyl in solution, as shown by ESIMS, forming a chemical

Externí odkaz: https://doaj.org/article/5ecdf8daf81448efb04436d2bb44d482

An enzyme-linked immunosorbent assay for the detection of diacetyl (2,3-butanedione)

Autor: Lucia Marri, Ole Hindsgaul, Anita M. Jansson, Caspar Christensen

Publikováno v: Analytical Biochemistry. 535:12-18

Diacetyl (2,3-butanedione) is an important metabolic marker of several cancers, as well as an important off-flavour component produced during fermentation. As a small molecule in a complex mixture with many other analytes, existing methods for identi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ec2b0bfd60e38607f0f6209b13eb01d
https://doi.org/10.1016/j.ab.2017.07.021

Structure of branching enzyme- and amylomaltase modified starch produced from well-defined amylose to amylopectin substrates

Autor: Kim H. Hebelstrup, Sunanta Tongta, Byung-Hoo Lee, Agnès Rolland-Sabaté, Sebastian Meier, Waraporn Sorndech, Andreas Blennow, Anita M. Jansson, Domenico Sagnelli, Bruce R. Hamaker

Publikováno v: Carbohydrate Polymers
Carbohydrate Polymers, Elsevier, 2016, 152, pp.51-61. ⟨10.1016/j.carbpol.2016.06.097⟩
Sorndech, W, Sagnelli, D, Meier, S, Jansson, A M, Lee, B H, Hamaker, B R, Rolland-Sabaté, A, Hebelstrup, K H, Tongta, S & Blennow, A 2016, ' Structure of branching enzyme-and amylomaltase modified starch produced from well-defined amylose to amylopectin substrates ', Carbohydrate Polymers, vol. 152, pp. 51-61 . https://doi.org/10.1016/j.carbpol.2016.06.097
Sorndecha, W, Sagnelli, D, Meier, S, Jansson, A M, Lee, B-H, Hamaker, B R, Rolland-Sabaté, A, Hebelstrup, K H, Tongta, S & Blennow, A 2016, ' Structure of branching enzyme-and amylomaltase modified starch produced from well-defined amylose to amylopectin substrates ', Carbohydrate Polymers, vol. 152, pp. 51-61 . https://doi.org/10.1016/j.carbpol.2016.06.097

Thermostable branching enzyme (BE, EC 2.4.1.18) from Rhodothermus obamensis in combination with amylomaltase (AM, EC 2.4.1.25) from Thermus thermophilus was used to modify starch structure exploring potentials to extensively increase the number of br

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f2a8076cfb28eae436318e46c3142c7
https://hal.inrae.fr/hal-02638851

Synthesis and application of sialic acid-containing building blocks for glycopeptide libraries. Establishing glycosylation conditions

Autor: Morten Meldal, Anita M. Jansson, Phaedria M. St. Hilaire, Koen M. Halkes, Charlotte Held Gotfredsen

Publikováno v: Journal of the Chemical Society, Perkin Transactions 1. :2127-2133

Three different sialic acid-containing building blocks (6–8) were synthesized for use in solid-phase glycopeptide libraries. Investigation of the conditions for glycosylation of threonine (Thr) with various sialic acid donors revealed that the best

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::89ef8c9f539e3c4cf21b6f8e14aefeac
https://doi.org/10.1039/a908321i

Silyl protection in the solid-phase synthesis of N-linked glycopeptides. Preparation of glycosylated fluorogenic substrates for subtilisins

Autor: Anita M. Jansson, Klaus Bock, Klaus Breddam, Morten Meldal, Ida Christiansen-Brams

Publikováno v: Bioorganic & Medicinal Chemistry. 2:1153-1167

The trimethylsilyl (TMS) group was used for protection of the hydroxy groups of three disaccharide 1-amino-alditols and of the glycosylamines of glucose, maltotriose and maltoheptose. The per-O-trimethylsilylated derivatives were coupled with N alpha

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f41ddd7804e83c2250356738bece7cc
https://doi.org/10.1016/s0968-0896(00)82067-2