Degradation of the thiocarbamate herbicide EPTC (S-ethyl dipropylcarbamothioate) and biosafening by Rhodococcus sp. strain NI86/21 involve an inducible cytochrome P-450 system and aldehyde…
- I. Nagy, G. Schoofs, F. Compernolle, P. Proost, J. Vanderleyden, R. De Mot
- BiologyJournal of Bacteriology
- 1 February 1995
It was demonstrated that the aldehyde dehydrogenase gene is widespread in the Rhodococcus genus, but the components of the cytochrome P-450 system are unique to Rhoditis sp.
A single cytochrome P-450 system is involved in degradation of the herbicides EPTC (S-ethyl dipropylthiocarbamate) and atrazine by Rhodococcus sp. strain NI86/21
- I. Nagy, F. Compernolle, Karen Ghys, J. Vanderleyden, R. De Mot
- BiologyApplied and Environmental Microbiology
- 1 May 1995
During atrazine degradation by Rhodococcus sp. strain N186/21, N-dealkylated metabolites and an hydroxyisopropyl derivative are produced. The cytochrome P-450 system that is involved in degradation…
Biohydrogenation of sterols by Eubacterium ATCC 21,408--Nova species.
- H. Eyssen, G. Parmentier, F. Compernolle, G. De Pauw, M. Piessens-denef
- Chemistry, BiologyEuropean Journal of Biochemistry
- 1 July 1973
Eubacterium 21,408, a strictly anaerobic bacterium, was isolated from rat cecal contents by its requirements for a Δ5-3β-hydroxy steroid and reduced the 5,6-double bond of cholesterol, campesterol, β-sitosterol and stigmasterol, exclusively yielding the corresponding 5β-saturated derivatives.
Identification of steviol glucuronide in human urine.
- J. Geuns, J. Buyse, A. Vankeirsbilck, E. Temme, F. Compernolle, S. Toppet
- Biology, MedicineJournal of Agricultural and Food Chemistry
- 4 March 2006
This is the first report on the unambiguous identification of steviol glucuronide in human urine by MS, NMR, IR, and UV spectroscopy.
Cloning and heterologous expression of early genes in gibberellin and steviol biosynthesis via the methylerythritol phosphate pathway in Stevia rebaudiana
- N. Totté, W. Ende, E. Damme, F. Compernolle, Ilse Baboeuf, J. Geuns
- Biology
- 2003
The ent-kaurene skeleton of chloroplast diterpene glycosides, which are produced in large quantities in the leaves of Stevia rebaudiana Bertoni, is formed via the recently discovered 2-C-methyl-D-erythritol 4-phosphate pathway and it is demonstrated through heterologous expression in Escherichia coli that the cloned cDNAs encode functional proteins.
Study of the carbonyl products of terpene/OH radical reactions: detection of the 2,4-DNPH derivatives by HPLC-MS
- V. Bergh, H. Coeckelberghs, H. Vankerckhoven, F. Compernolle, C. Vinckier
- ChemistryAnalytical and Bioanalytical Chemistry
- 30 April 2004
The oxidation of the terpenes α- and β-pinene, limonene and Δ3-carene by hydroxyl radicals has been investigated in a fast-flow reactor coupled to a liquid nitrogen trap for collecting the carbonyl…
Product yields of the alpha-pinene reaction with hydroxyl radicals and the implication on the global emission of trace compounds in the atmosphere
- C. Vinckier, F. Compernolle, A. Saleh, N. V. Hoof, I. Hees
- Environmental Science
- 1998
Biosynthesis of the diterpenoid steviol, an ent-kaurene derivative from Stevia rebaudiana Bertoni, via the methylerythritol phosphate pathway
- N. Totté, L. Charon, M. Rohmer, F. Compernolle, Ilse Baboeuf, J. Geuns
- Chemistry
- 12 August 2000
Mass spectral evidence for N-glycans with branching on fucose in a molluscan hemocyanin.
- C. Gielens, K. Idakieva, V. Van den Bergh, N. I. Siddiqui, K. Parvanova, F. Compernolle
- Biology, ChemistryBiochemical and Biophysical Research…
- 3 June 2005
The fate of bilirubin-IXalpha glucuronide in cholestasis and during storage in vitro. Intramolecular rearrangement to positional isomers of glucuronic acid.
- N. Blanckaert, F. Compernolle, P. Leroy, R. Van Houtte, J. Fevery, K. Heirwegh
- Biology, Computer ScienceBiochemical Journal
- 1 April 1978
The mixtures of the four positional isomers of bilirubin-IXalpha glucuronide found in freshly collected biles of man and rats with cholestasis probably originate from initially synthesized 1-O-acylglucuronide by the same mechanism of sequential migration as has been observed in aqueous solutions of conjugated bilirube-IX alpha.
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