Geschmack ist vorhersagbar: Mit FlavorMiner. FlavorMiner heißt das Tool, das IPB-Chemiker und Partner aus Kolumbien jüngst entwickelt haben. Das Programm kann, basierend auf maschinellem Lernen (KI), anhand der…
Seit Februar 2021 bietet Wolfgang Brandt, ehemaliger Leiter der Arbeitsgruppe Computerchemie am IPB, sein Citizen Science-Projekt zur Pilzbestimmung an. Dafür hat er in regelmäßigen Abständen öffentliche Vorträge zur Vielfalt…
Jouda, J.-B.; Njoya, E. M.; Fobofou, S. A. T.; Zhou, Z. Y.; Qiang, Z.; Mbazoa, C. D.; Brandt, W.; Zhang, G.-l.; Wandji, J.; Wang, F.;Natural Polyketides Isolated from the Endophytic Fungus
Phomopsis sp. CAM212 with a Semisynthetic Derivative Downregulating
the ERK/IκBα Signaling PathwaysPlanta Med.861032-1042(2020)DOI: 10.1055/a-1212-2930
AbstractThree previously undescribed natural products, phomopsinin A – C
(1 – 3), together with three known compounds, namely,
cis-hydroxymellein (4), phomoxanthone A (5) and
cytochalasin L-696,474 (6), were isolated from the solid culture of
Phomopsis sp. CAM212, an endophytic fungus obtained from Garcinia
xanthochymus. Their structures were determined on the basis of
spectroscopic data, including IR, NMR, and MS. The absolute configurations of
1 and 2 were assigned by comparing their experimental and
calculated ECD spectra. Acetylation of compound 1 yielded 1a, a
new natural product derivative that was tested together with other isolated
compounds on lipopolysaccharide-stimulated RAW 264.7 cells. Cytochalasin
L-696,474 (6) was found to significantly inhibit nitric oxide production,
but was highly cytotoxic to the treated cells, whereas compound 1
slightly inhibited nitric oxide production, which was not significantly
different compared to lipopolysaccharide-treated cells. Remarkably, the
acetylated derivative of 1, compound 1a, significantly inhibited
nitric oxide production with an IC50 value of 14.8 µM and no
cytotoxic effect on treated cells, thereby showing the importance of the acetyl
group in the anti-inflammatory activity of 1a. The study of the mechanism
of action revealed that 1a decreases the expression of inducible nitric
oxide synthase, cyclooxygenase 2, and proinflammatory cytokine IL-6 without an
effect on IL-1β expression. Moreover, it was found that 1a exerts
its anti-inflammatory activity in lipopolysaccharide-stimulated RAW 264.7
macrophage cells by downregulating the activation of ERK1/2 and by preventing
the translocation of nuclear factor κB. Thus, derivatives of phomopsinin
A (1), such as compound 1a, could provide new anti-inflammatory
leads.
Publikation
Müller, H.; Heinze, M.; Heinke, R.; Schmidt, J.; Roos, W.;Self-regulation of phytoalexin production: a non-biosynthetic enzyme controls alkaloid biosynthesis in cultured cells of Eschscholzia californicaPlant Cell Tiss. Organ Cult.119661-676(2014)DOI: 10.1007/s11240-014-0565-6
Benzophenanthridine alkaloids are strong antimicrobials of Papaveraceae and attractive lead compounds for drug development. The cytotoxicity of these compounds requires the producing plant to limit the pathogen-triggered burst of biosynthesis. Cells of Eschscholzia californica excrete early benzophenanthridines to the cell wall, followed by re-uptake and reduction in the cytoplasm by the detoxifying enzyme sanguinarine reductase. We now discovered that this enzyme is a core component of self-control in alkaloid production. RNAi-based silencing of sanguinarine reductase gave rise to mutants that either show a complete stop of elicitor-triggered alkaloid production or a burst of biosynthesis that severalfold surpasses the wild type level. These unexpected phenotypes reflect impacts of substrate or product of sanguinarine reductase: the substrate, sanguinarine, inhibits phospholipase A2 at the plasma membrane, an initial component of the signal path towards expression of biosynthetic enzymes. The product, dihydrosanguinarine, inhibits enzymes of early biosynthesis, prior to reticuline formation. By tuning these steady states, sanguinarine reductase adjusts the capacity of alkaloid biosynthesis: a minimum activity is sufficient to prevent the blockade of the induction pathway by sanguinarine, while the full activity of the same enzyme causes a limitation of the biosynthetic flow via dihydrosanguinarine.
Publikation
Farag, M. A.; Wessjohann, L. A.;Metabolome Classification of Commercial Hypericum perforatum (St. John's Wort) Preparations via UPLC-qTOF-MS and ChemometricsPlanta Med.78488-496(2012)DOI: 10.1055/s-0031-1298170
The growing interest in the efficacy of phytomedicines and herbal supplements but also the increase in legal requirements for safety and reliable contents of active principles drive the development of analytical methods for the quality control of complex, multicomponent mixtures as found in plant extracts of value for the pharmaceutical industry. Here, we describe an ultra-performance liquid chromatography method (UPLC) coupled with quadrupole time of flight mass spectrometry (qTOF-MS) measurements for the large scale analysis of H. perforatum plant material and its commercial preparations. Under optimized conditions, we were able to simultaneously quantify and identify 21 metabolites including 4 hyperforins, 3 catechins, 3 naphthodianthrones, 5 flavonoids, 3 fatty acids, and a phenolic acid. Principal component analysis (PCA) was used to ensure good analytical rigorousness and define both similarities and differences among Hypericum samples. A selection of batches from 9 commercially available H. perforatum products available on the German and Egyptian markets showed variable quality, particularly in hyperforins and fatty acid content. PCA analysis was able to discriminate between various preparations according to their global composition, including differentiation between various batches from the same supplier. To the best of our knowledge, this study provides the first approach utilizing UPLC-MS-based metabolic fingerprinting to reveal secondary metabolite compositional differences in Hypericum extract.
Publikation
Ramos Leal, I. C.; Netto dos Santos, K. R.; Itabaiana Júnior, I.; Ceva Antunes, O. A.; Porzel, A.; Wessjohann, L.; Machado Kuster, R.;Ceanothane and Lupane Type Triterpenes from Zizyphus joazeiro – An Anti-Staphylococcal EvaluationPlanta Med.7647-52(2010)DOI: 10.1055/s-0029-1185947
The present paper describes the phytochemical and anti-staphylococcal activity investigation of the dichloromethane extract of the Brazilian plant Zizyphus joazeiro Mart. The purification steps were guided by bioassays against 17 bacterial strains of clinical sources, including methicillin-resistant (MRSA) and ‐sensitive (MSSA) Staphylococcus aureus as well as MRSA (ATCC 33591) and MSSA (ATCC 29213) reference strains. One of the more active fractions is comprised of three lupane-type triterpenes, the methylbetulinate (1) as well as the known betulinic (2) and alphitolic (3) acids and, for the first time in the Z. joazeiro, two ceanothane type triterpenes, the methylceanothate (4) and the epigouanic acid A (5). These substances were assayed against one clinical (PVL+) and the reference strains of S. aureus as well as the ATTC 12228 strain of S. epidermidis, in concentrations that varied from 128 to 0.125 µg/mL in order to establish the minimum inhibitory concentration (MIC) of the drugs. The minimum bactericide concentration (MBC) was also evaluated to distinguish the bactericidal from bacteriostatic activity of the crude fractions and single compounds. Compounds 3 and 4 possess the highest antibacterial activity. They inhibit all bacteria tested at 32 µg/mL and 16 µg/mL, respectively, while the other compounds showed no activity at 128 µg/mL. In contrast to single compounds, the triterpenoid fraction showed bactericidal activity at 256 µg/mL. Structural elucidations are based on 1D and 2D NMR spectroscopy as well as HR‐FT‐ICR‐MS experiments.