Ludger Beerhues

Prof. Ludger Beerhues


Research Focus & Metrics

Academic Career Length

42Years (1985-Present)

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

Representative Publications

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19 May 2017 in Journal of Pharmacy and Pharmacology
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PSPreeti Shakya
Preeti Shakya
MGMarslin Gregory
Marslin Gregory
KSKarthik Siram
Karthik Siram
LBLudger Beerhues
Ludger Beerhues
GFGregory Franklin
Gregory Franklin
Objectives: In this review, we aim at updating the available information on the improvement of the Hypericum perforatum L. (Hypericaceae) phytochemical profile and pharmacological properties via elicitation. Key findings: Hypericum perforatum seedlings, shoots, roots, calli and cell suspension cultures were treated with diverse elicitors to induce the formation of secondary metabolites. The extracts of the elicitor-treated plant material containing naphthodianthrones, phloroglucinols, xanthones, flavonoids and other new compounds were quantitatively analysed and tested for their bioactivities. While hypericins were mainly produced in H. perforatum cultures containing dark nodules, namely shoots and seedlings, other classes of compounds such as xanthones, phloroglucinols and flavonoids were formed in all types of cultures. The extracts obtained from elicitor-treated samples generally possessed better bioactivities compared to the extract of control biomass. Summary: Although elicitation is an excellent tool for the production of valuable secondary metabolites in H. perforatum cell and tissue cultures, its exploitation is still in its infancy mainly due to the lack of reproducibility and difficulties in scaling up biomass production.

1 February 2010 in Phytochemistry
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NSNicholas Schramek
Nicholas Schramek
HWHuahong Wang
Huahong Wang
WRWerner Römisch-Margl
Werner Römisch-Margl
BKBirgit Keil
Birgit Keil
TRTanja Radykewicz
Tanja Radykewicz
WEWolfgang Eisenreich
Wolfgang Eisenreich

1 October 2006 in Phytochemistry
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Journal Article
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LBLudger Beerhues
Ludger Beerhues

10 June 2003 in The Plant Journal
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BLBenye Liu
Benye Liu
HFHildegard Falkenstein‐Paul
Hildegard Falkenstein‐Paul
WSWerner Schmidt
Werner Schmidt
LBLudger Beerhues
Ludger Beerhues
Summary: Benzophenone derivatives, such as polyprenylated benzoylphloroglucinols and xanthones, are biologically active secondary metabolites. The formation of their C13 skeleton is catalyzed by benzophenone synthase (BPS; EC 2.3.1.151) that has been cloned from cell cultures of Hypericum androsaemum. BPS is a novel member of the superfamily of plant polyketide synthases (PKSs), also termed type III PKSs, with 53–63% amino acid sequence identity. Heterologously expressed BPS was a homodimer with a subunit molecular mass of 42.8 kDa. Its preferred starter substrate was benzoyl‐CoA that was stepwise condensed with three malonyl‐CoAs to give 2,4,6‐trihydroxybenzophenone. BPS did not accept activated cinnamic acids as starter molecules. In contrast, recombinant chalcone synthase (CHS; EC 2.3.1.74) from the same cell cultures preferentially used 4‐coumaroyl‐CoA and also converted CoA esters of benzoic acids. The enzyme shared 60.1% amino acid sequence identity with BPS. In a phylogenetic tree, the two PKSs occurred in different clusters. One cluster was formed by CHSs including the one from H. androsaemum. BPS grouped together with the PKSs that functionally differ from CHS. Site‐directed mutagenesis of amino acids shaping the initiation/elongation cavity of CHS yielded a triple mutant (L263M/F265Y/S338G) that preferred benzoyl‐CoA over 4‐coumaroyl‐CoA.

1 March 2002 in Planta
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AEAbd El-Mawla
Abd El-Mawla
AMAhmed M.
Ahmed M.
LBLudger Beerhues
Ludger Beerhues

20 April 2012 in Beilstein Journal of Organic Chemistry
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CCCornelia Chizzali
Cornelia Chizzali
LBLudger Beerhues
Ludger Beerhues
Biphenyls and dibenzofurans are the phytoalexins of the Pyrinae, a subtribe of the plant family Rosaceae. The Pyrinae correspond to the long-recognized Maloideae. Economically valuable species of the Pyrinae are apples and pears. Biphenyls and dibenzofurans are formed de novo in response to infection by bacterial and fungal pathogens. The inducible defense compounds were also produced in cell suspension cultures after treatment with biotic and abiotic elicitors. The antimicrobial activity of the phytoalexins was demonstrated. To date, 10 biphenyls and 17 dibenzofurans were isolated from 14 of the 30 Pyrinae genera. The most widely distributed compounds are the biphenyl aucuparin and the dibenzofuran γ-cotonefuran. The biosynthesis of the two classes of defense compounds is not well understood, despite the importance of the fruit crops. More recent studies have revealed simultaneous accumulation of biphenyls and dibenzofurans, suggesting sequential, rather than the previously proposed parallel, biosynthetic pathways. Elicitor-treated cell cultures of Sorbus aucuparia served as a model system for studying phytoalexin metabolism. The key enzyme that forms the carbon skeleton is biphenyl synthase. The starter substrate for this type-III polyketide synthase is benzoyl-CoA. In apples, biphenyl synthase is encoded by a gene family, members of which are differentially regulated. Metabolism of the phytoalexins may provide new tools for designing disease control strategies for fruit trees of the Pyrinae subtribe.