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2 article(s) from Brinkhoff, Thorsten

N-Acylated amino acid methyl esters from marine Roseobacter group bacteria

Hilke Bruns,
Lisa Ziesche,
Nargis Khakin Taniwal,
Laura Wolter,
Thorsten Brinkhoff,
Jennifer Herrmann,
Rolf Müller and
Stefan Schulz

Beilstein J. Org. Chem. 2018, 14, 2964–2973, doi:10.3762/bjoc.14.276

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Figure 1: N-Acylhomoserine lactones 1 (Z7-C14:1-AHL) and N-acylalanine methyl esters 2 (Z9-C16:1-NAME) occurr...

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Figure 2: Total ion chromatogram (TIC) of an XAD extract of Roseovarius sp. D12_1.68. AHLs, NAMEs and related...

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Scheme 1: Synthesis of iso-C15:0-NAME (6). DMAP: 4-dimethylaminopyridine, EDC: 1-ethyl-3-(3-dimethylaminoprop...

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Figure 3: Mass spectrum of natural compound D, N-(13-methyltetradecanoyl)alanine methyl ester (iso-C15:0-NAME...

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Figure 4: Mass spectra of natural compounds a) K (7, C16:0-NABME), b) J (8, C16:1-NABME), and c) N (9, C16:1-...

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Scheme 2: Synthesis of N-acylated amino acid methyl esters 7–11. AAME: amino acid methyl ester.

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Figure 5: TIC of an XAD extract of Loktanella sp. F14. Compound S is a minor component within the broad peak.

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Figure 6: Mass spectra of natural compounds a) R (11, C16:1-NAGME) and b) S (10, C16:0-NAGME).

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Figure 7: EI mass spectrometric fragmentation of N-acylated amino acid derivatives. The ions w–z allow identi...

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Figure 8: MS² spectra in ESI positive mode of a) Z9-16OH-C16:1-NAME with [M + H − H₂O]⁺ 356, b) Z9-C16:1-NABM...

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Published 03 Dec 2018

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Isotopically labeled sulfur compounds and synthetic selenium and tellurium analogues to study sulfur metabolism in marine bacteria

Nelson L. Brock,
Christian A. Citron,
Claudia Zell,
Martine Berger,
Irene Wagner-Döbler,
Jörn Petersen,
Thorsten Brinkhoff,
Meinhard Simon and
Jeroen S. Dickschat

Beilstein J. Org. Chem. 2013, 9, 942–950, doi:10.3762/bjoc.9.108

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Figure 1: Roseobacter clade metabolites.

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Scheme 1: Degradation of DMSP via (A) demethylation pathway and (B) cleavage pathways. FH₄: tetrahydrofolate.

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Scheme 2: Sulfate reduction pathway and incorporation of sulfur into the amino acid pool. PAP: adenosine 3’,5...

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Figure 2: Volatiles from P. gallaeciensis DSM 17395 and R. pomeroyi DSS-3. Feeding of [²H₆]DMSP results in de...

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Figure 3: Chromatograms of headspace extracts from P. gallaeciensis DSM 17395 after feeding of DMTeP by the u...

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Figure 4: Chromatograms of headspace extracts obtained after feeding of [²H₆]DMSP by the use of SPME from (A) ...

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Figure 5: Chromatograms of headspace extracts from (A) R. pomeroyi DSS-3 wild type, (B) R. pomeroyi DSS-3 dmdA...

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Scheme 3: Synthesis of ³⁴S-labeled thiosulfate and sulfate.

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Figure 6: Volatiles from P. gallaeciensis after feeding of selenate and selenite.

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Figure 7: Chromatograms of headspace extracts from P. gallaeciensis grown on (A) 50% MB2216, (B) 50% MB2216 +...

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Figure 8: Additional sulfur volatiles.

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Published 15 May 2013

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