Literature DB >> 26841051

Biochemometrics for Natural Products Research: Comparison of Data Analysis Approaches and Application to Identification of Bioactive Compounds.

Joshua J Kellogg1, Daniel A Todd1, Joseph M Egan1, Huzefa A Raja1, Nicholas H Oberlies1, Olav M Kvalheim2, Nadja B Cech1.   

Abstract

A central challenge of natural products research is assigning bioactive compounds from complex mixtures. The gold standard approach to address this challenge, bioassay-guided fractionation, is often biased toward abundant, rather than bioactive, mixture components. This study evaluated the combination of bioassay-guided fractionation with untargeted metabolite profiling to improve active component identification early in the fractionation process. Key to this methodology was statistical modeling of the integrated biological and chemical data sets (biochemometric analysis). Three data analysis approaches for biochemometric analysis were compared, namely, partial least-squares loading vectors, S-plots, and the selectivity ratio. Extracts from the endophytic fungi Alternaria sp. and Pyrenochaeta sp. with antimicrobial activity against Staphylococcus aureus served as test cases. Biochemometric analysis incorporating the selectivity ratio performed best in identifying bioactive ions from these extracts early in the fractionation process, yielding altersetin (3, MIC 0.23 μg/mL) and macrosphelide A (4, MIC 75 μg/mL) as antibacterial constituents from Alternaria sp. and Pyrenochaeta sp., respectively. This study demonstrates the potential of biochemometrics coupled with bioassay-guided fractionation to identify bioactive mixture components. A benefit of this approach is the ability to integrate multiple stages of fractionation and bioassay data into a single analysis.

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Year:  2016        PMID: 26841051      PMCID: PMC5135737          DOI: 10.1021/acs.jnatprod.5b01014

Source DB:  PubMed          Journal:  J Nat Prod        ISSN: 0163-3864            Impact factor:   4.050


  36 in total

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7.  Inducible NorA-mediated multidrug resistance in Staphylococcus aureus.

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  46 in total

1.  Simplify: A Mass Spectrometry Metabolomics Approach to Identify Additives and Synergists from Complex Mixtures.

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Review 5.  Synergy and antagonism in natural product extracts: when 1 + 1 does not equal 2.

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6.  A metabolomics guided exploration of marine natural product chemical space.

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7.  Opportunities and Limitations for Untargeted Mass Spectrometry Metabolomics to Identify Biologically Active Constituents in Complex Natural Product Mixtures.

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8.  Conventional and accelerated-solvent extractions of green tea (camellia sinensis) for metabolomics-based chemometrics.

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10.  Evaluating Sufficient Similarity of Botanical Dietary Supplements: Combining Chemical and In Vitro Biological Data.

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Journal:  Toxicol Sci       Date:  2019-12-01       Impact factor: 4.849

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