Hartmut Laatsch

Prof. Dr. Hartmut Laatsch

Institute of Organic and Biomolecular Chemistry, University of Göttingen, Tammannstrasse 2, D-37077 Göttingen, Germany

Research Focus & Metrics

Academic Career Length

37Years (1990-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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9 April 2013 in European Journal of Organic Chemistry
Verified
Journal Article
Closed access
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FTFerdinand Mouafo Talontsi
Ferdinand Mouafo Talontsi
BDBirger Dittrich
Birger Dittrich
ASAnja Schüffler
Anja Schüffler
HSHan Sun
Han Sun
HLHartmut Laatsch
Hartmut Laatsch

18 November 2009 in Journal of Natural Products
Verified
Journal Article
Closed access
UHUsama Hawas
Usama Hawas
MSMohamed Shaaban
Mohamed Shaaban
Khaled A. ShaabanKhaled A. Shaaban
Khaled A. Shaaban
MSMichael Speitling
Michael Speitling
AMArmin Maier
Armin Maier
HLHartmut Laatsch
Hartmut Laatsch

1 January 2004 in The Journal of Antibiotics
Verified
Journal Article
Open access
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RARatnakar N. Asolkar
Ratnakar N. Asolkar
DSDirk Schröder
Dirk Schröder
RHRolf Heckmann
Rolf Heckmann
SLSiegmund Lang
Siegmund Lang
IWIrene Wagner-Döbler
Irene Wagner-Döbler
HLHartmut Laatsch
Hartmut Laatsch
The ethyl acetate extract of cultures of Janibacter limosus showed a high biological activity against bacteria, and fungi and delivered two new natural products, a tetrahydroquinoline derivative designated as helquinoline (1), and the N-acetylkynuramine (3a), along with other known secondary metabolites. The structure of 1 has been elucidated as 4-methoxy-2-methyl-1, 2, 3, 4-tetrahydroquinoline-8-carboxylic acid on the basis of 1D and 2D NMR and mass spectra. The relative stereochemistry of the compound 1 was assigned as 2R*, 4R* with the aid of coupling constants, NOESY correlation and by comparison with a related compound.

22 October 2010 in World Journal of Microbiology and Biotechnology
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Journal Article
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PRPornthip Ruanpanun
Pornthip Ruanpanun
HLHartmut Laatsch
Hartmut Laatsch
NTNuchanart Tangchitsomkid
Nuchanart Tangchitsomkid
SLSAISAMORN LUMYONG
SAISAMORN LUMYONG
An isolate of the actinomycete, Streptomyces sp. CMU-MH021 produced secondary metabolites that inhibited egg hatch and increased juvenile mortality of the root-knot nematode Meloidogyne incognita in vitro. 16S rDNA gene sequencing showed that the isolate sequence was 99% identical to Streptomyces roseoverticillatus. The culture filtrates form different culture media were tested for nematocidal activity. The maximal activity against M. incognita was obtained by using modified basal (MB) medium. The nematicidal assay-directed fractionation of the culture broth delivered fervenulin (1) and isocoumarin (2). Fervenulin, a low molecular weight compound, shows a broad range of biological activities. However, nematicidal activity of fervenulin was not previously reported. The nematicidal activity of fervenulin (1) was assessed using the broth microdilution technique. The lowest minimum inhibitory concentrations (MICs) of the compound against egg hatch of M. incognita was 30 μg/ml and juvenile mortality of M. incognita increasing was observed at 120 μg/ml. Moreover, at the concentration of 250 μg/ml fervenulin (1) showed killing effect on second-stage nematode juveniles of M. incognita up to 100% after incubation for 96 h. Isocoumarin (2), another bioactive compound produced by Streptomyces sp. CMU-MH021, showed weak nematicidal activity with M. incognita.

1 August 2005 in The Journal of Antibiotics
Verified
Journal Article
Open access
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IKInes Kock
Ines Kock
RMRajendra P Maskey
Rajendra P Maskey
MBM A Farooq Biabani
M A Farooq Biabani
EHElisabeth Helmke
Elisabeth Helmke
HLHartmut Laatsch
Hartmut Laatsch
Cultivation of the marine-derived streptomycete isolate B8005 delivered three known antibiotics, resistomycin (1), resistoflavin (3a) and tetracenomycin (4), and a further member of the rare resistomycin class, the weakly antibiotically active 1-hydroxy-1-norresistomycin (2). From a related marine strain B4842, 1 and resistoflavin methyl ether (3b) have been isolated. The formation of 2 is of interest from a biosynthetic point of view.

1 June 2006 in The Journal of Antibiotics
Verified
Journal Article
Closed access
SWShao Jie Wu
Shao Jie Wu
SFSerge Fotso
Serge Fotso
FLFuchao Li
Fuchao Li
SQSong Qin
Song Qin
GKGerhard Kelter
Gerhard Kelter
HLHartmut Laatsch
Hartmut Laatsch