Zobrazeno 1 - 10
of 58
pro vyhledávání: '"Jan Rinkel"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 17, Iss 1, Pp 420-430 (2021)
The volatiles emitted from six marine Rhodobacteraceae species of the genus Celeribacter were investigated by GC–MS. Besides several known compounds including dimethyl trisulfide and S-methyl methanethiosulfonate, the sulfur-containing compounds et
Externí odkaz:
https://doaj.org/article/0b34622807da4e62b3caaeff61be7fea
Autor:
Jan Rinkel, Jeroen S. Dickschat
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 15, Iss 1, Pp 1008-1019 (2019)
A bacterial terpene synthase from Cryptosporangium arvum was characterised as a multiproduct β-himachalene synthase. In vitro studies showed not only a high promiscuity with respect to its numerous sesquiterpene products, including the structurally
Externí odkaz:
https://doaj.org/article/5c3663531b794dc5bd9897f41f3217ee
Autor:
Jan Rinkel, Jeroen S. Dickschat
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 15, Iss 1, Pp 789-794 (2019)
A newly identified bacterial (Z)-γ-bisabolene synthase was used for investigating the cyclisation mechanism of the sesquiterpene. Since the stereoinformation of both chiral putative intermediates, nerolidyl diphosphate (NPP) and the bisabolyl cation
Externí odkaz:
https://doaj.org/article/2f835451dce242d6b257cbfbb8e8233a
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 2974-2990 (2018)
The volatiles emitted by the ascomycetes Hypoxylon griseobrunneum and Hypoxylon macrocarpum (Hypoxylaceae, Xylariales) were collected by use of a closed-loop stripping apparatus (CLSA) and analysed by GC–MS. The main compound class of both species
Externí odkaz:
https://doaj.org/article/d9fdd534a1fa40e0a75cddc8116754d1
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 1309-1316 (2018)
N-Acylhomoserine lactones (AHLs) are important bacterial messengers, mediating different bacterial traits by quorum sensing in a cell-density dependent manner. AHLs are also produced by many bacteria of the marine Roseobacter group, which constitutes
Externí odkaz:
https://doaj.org/article/1b5f41b8ebc44d338f51906a791b946c
Autor:
Jeroen S. Dickschat, Jan Rinkel, Patrick Rabe, Arman Beyraghdar Kashkooli, Harro J. Bouwmeester
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 13, Iss 1, Pp 1770-1780 (2017)
The product obtained in vitro from a diterpene synthase encoded in the genome of the bacterium Chitinophaga pinensis, an enzyme previously reported to have germacrene A synthase activity during heterologous expression in Escherichia coli, was identif
Externí odkaz:
https://doaj.org/article/d6984223210d45fb9ee0a4d4613b853d
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 12, Iss 1, Pp 2317-2324 (2016)
The stereochemical course of the cyclisation reaction catalysed by the bacterial 1,8-cineol synthase from Streptomyces clavuligerus was investigated using stereospecifically deuterated substrates. In contrast to the well investigated plant enzyme fro
Externí odkaz:
https://doaj.org/article/c616bf18a409451ea9d208536603b02a
Autor:
Jan Rinkel, Jeroen S. Dickschat
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 11, Iss 1, Pp 2493-2508 (2015)
The long and successful history of isotopic labeling experiments within natural products research has both changed and deepened our understanding of biosynthesis. As demonstrated in this article, the usage of isotopes is not at all old-fashioned, but
Externí odkaz:
https://doaj.org/article/8a05f1136d67476281878775db04b761
Publikováno v:
Organic & Biomolecular Chemistry. 19:370-374
The main product of DpTPS9 from the social amoeba Dictyostelium purpureum was identified as (4S,7R)-germacra-(1(10)E,5E)-dien-11-ol that is also known as an intermediate of bacterial geosmin synthase, but the experimentally verified cyclisation mecha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::80b00b0bfc55bd4fe95f20d05fac4888
https://doi.org/10.1039/d0ob02361b
https://doi.org/10.1039/d0ob02361b
Publikováno v:
Organic Chemistry Frontiers. 8:1177-1184
A new sesquiterpene synthase from Streptomyces lincolnensis was identified as isoishwarane synthase. The absolute configuration of its product was determined by an enantioselective deuteration strategy. The cyclisation mechanism from farnesyl diphosp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bc57d0a98cb4b88822ae916f5b663c45
https://doi.org/10.1039/d0qo01583k
https://doi.org/10.1039/d0qo01583k