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1.
World J Microbiol Biotechnol ; 35(11): 167, 2019 Oct 24.
Article in English | MEDLINE | ID: mdl-31650344

ABSTRACT

Codium tomentosum, as all organisms, hosts transiently and permanently numerous microorganisms. These holobionts can undergo environmental pressures influencing both partners creating modifications/imbalances within the associations, which may directly influence their physiological status by selecting tolerant bacteria. Furthermore, the capability of remediation of the associated bacterioflora, in particular of metallic trace elements, may provide the host with survival potential in polluted environments. In this context, we incubated C. tomentosum thalli in the presence of copper and studied its influence on the reference bacteriome. Whatever the concentration of copper, no shift was evidenced on the bacteriome at the phylum level. However, a high copper concentration enriched the bacteriome of C. tomentosum in both the genera Clostridium and Pseudolteromonas.


Subject(s)
Bacteria/classification , Bacteria/drug effects , Chlorophyta/microbiology , Copper/toxicity , Microbiota/drug effects , Bacteria/isolation & purification , Bacteria/metabolism , Biodiversity , Microbiota/physiology , Seawater/chemistry , Seawater/microbiology , Seaweed/microbiology , Trace Elements , Water Pollutants
2.
Methods Mol Biol ; 1308: 131-43, 2015.
Article in English | MEDLINE | ID: mdl-26108502

ABSTRACT

The interest in the physiological roles and bioactivities of plant phenols has increased over the past decades. In seaweeds, many investigations have dealt with phenolic compounds of Phaeophyceae (phlorotannins), even though little is known so far about the ecophysiological variations of their pool or their biosynthetic pathways. We describe here a simple procedure based on the use of water-organic solvent mixtures for the extraction of phlorotannins. Crude extracts are semi-purified and fractionated by separating methods based on both the polarity and the molecular size of compounds. Phenols are then quantified by the Folin-Ciocalteu method and their radical-scavenging activity is characterized using the DPPH test. All along the purification process of phenolic compounds, the efficiency of separation is assessed by (1)H-NMR.


Subject(s)
Free Radical Scavengers/isolation & purification , Phaeophyceae/chemistry , Phenols/isolation & purification , Tannins/isolation & purification , Free Radical Scavengers/chemistry , Free Radical Scavengers/pharmacology , Liquid-Liquid Extraction/methods , Phenols/chemistry , Phenols/pharmacology , Proton Magnetic Resonance Spectroscopy/methods , Seaweed/chemistry , Solvents/chemistry , Tannins/chemistry , Tannins/pharmacology , Water/chemistry
3.
Plant Cell ; 25(8): 3089-103, 2013 Aug.
Article in English | MEDLINE | ID: mdl-23983220

ABSTRACT

Brown algal phlorotannins are structural analogs of condensed tannins in terrestrial plants and, like plant phenols, they have numerous biological functions. Despite their importance in brown algae, phlorotannin biosynthetic pathways have been poorly characterized at the molecular level. We found that a predicted type III polyketide synthase in the genome of the brown alga Ectocarpus siliculosus, PKS1, catalyzes a major step in the biosynthetic pathway of phlorotannins (i.e., the synthesis of phloroglucinol monomers from malonyl-CoA). The crystal structure of PKS1 at 2.85-Å resolution provided a good quality electron density map showing a modified Cys residue, likely connected to a long chain acyl group. An additional pocket not found in other known type III PKSs contains a reaction product that might correspond to a phloroglucinol precursor. In vivo, we also found a positive correlation between the phloroglucinol content and the PKS III gene expression level in cells of a strain of Ectocarpus adapted to freshwater during its reacclimation to seawater. The evolution of the type III PKS gene family in Stramenopiles suggests a lateral gene transfer event from an actinobacterium.


Subject(s)
Biosynthetic Pathways , Phaeophyceae/enzymology , Polyketide Synthases/chemistry , Polyketide Synthases/metabolism , Tannins/biosynthesis , Acclimatization , Amino Acid Sequence , Catalytic Domain , Crystallography, X-Ray , Fresh Water , Gene Expression Regulation, Enzymologic , Gene Expression Regulation, Plant , Models, Molecular , Molecular Sequence Data , Phaeophyceae/genetics , Phloroglucinol/chemistry , Phloroglucinol/metabolism , Phylogeny , Polyketide Synthases/genetics , RNA, Messenger/genetics , RNA, Messenger/metabolism , Recombinant Proteins/metabolism , Seawater , Sequence Alignment , Structure-Activity Relationship , Tannins/chemistry
4.
Talanta ; 86: 362-71, 2011 Oct 30.
Article in English | MEDLINE | ID: mdl-22063552

ABSTRACT

Sunscreen efficiency of biomolecules against UV-B radiation was generally determined in vitro by cosmetic methods which are not well-adapted for routine ecophysiological and bio-guidance studies in plant research laboratories. In this article, we propose a new in vitro method to evaluate the sunscreen photoprotective activity of plant extracts against high UV-B radiation. Because photosynthetic pigments are one of the first targets of UV-B radiation in plants, the experimental design is based on the ability of the tested substances to limit the degradation of sodium magnesium chlorophyllin (SMC), a derivative compound of natural chlorophyll. SMC photodegradation comparatively to natural chlorophyll and related to temperature, concentration and sample solvent were analyzed in order to optimize the experimental parameters. Then, the method was validated by testing nine standard UV filters used in the European cosmetic industry and by comparing results of their activity with those of a reference in vitro procedure. Finally, the method was applied to coastal and marine crude plant extracts. Results have shown that our procedure can be a good alternative to cosmetic methods with a rapid, sensitive and reproducible evaluation of the sunscreen activity of either pure standards or crude plant extracts in small amounts (30 mg).


Subject(s)
Drug Evaluation, Preclinical/methods , Plant Extracts/analysis , Sunscreening Agents/analysis , Ultraviolet Rays , Plant Extracts/chemistry , Sunscreening Agents/chemistry , Ultraviolet Rays/adverse effects
5.
Talanta ; 84(2): 513-8, 2011 Apr 15.
Article in English | MEDLINE | ID: mdl-21376981

ABSTRACT

In this article, the radical-scavenging capacity of phenol fractions extracted from the brown seaweed Ascophyllum nodosum was assessed using in parallel colorimetric methods (ABTS and DPPH) and electrochemistry (cyclic voltammetry). Results obtained by the three methods correlated in the case of global fractions, whereas only ABTS and DPPH correlated when activities were expressed on a phenol basis. The successive fractions separated by both their average molecular size and their polarity exhibited activities largely dependent on their phenol content, suggesting that phlorotannins are the main anti-oxidant molecules in hydro-alcoholic extracts of A. nodosum. In addition, phenol fractions of relative low molecular weight were clearly more active than others. This work opens new opportunities to better evaluate the radical-scavenging potential of phenol pools in algae using both bi-parametric fractionating and electrochemistry.


Subject(s)
Antioxidants/pharmacology , Electrochemistry/methods , Free Radical Scavengers/pharmacology , Phenols/pharmacology , Seaweed/chemistry
6.
Phytochem Anal ; 21(5): 399-405, 2010.
Article in English | MEDLINE | ID: mdl-20333652

ABSTRACT

INTRODUCTION: Phenolic compounds are metabolites exhibited at high levels in Phaeophyceae. Although several studies have been conducted on total phenol contents, no one to our knowledge has dealt with the contents of phenolic compounds and antioxidant activities on purified fractions. OBJECTIVE: The purpose of this study was the extraction and purification of phenolic compounds from the brown seaweed Ascophylllum nodosum, to determine both their distribution and their radical-scavenging activities, and to obtain a sufficiently purified oligophenolic fraction to perform an RP-HPLC analysis on molecules with a molecular weight (MW) < 2 kDa. METHODOLOGY: Phenolic compounds were separated and purified by liquid-liquid extraction, tangential ultrafiltration and dialysis. Then, the contents of both phenolic compounds and radical-scavenging activities were measured by the Folin-Ciocalteu reagent, and DPPH and ABTS assays. NMR analysis was performed to validate the process. RP-HPLC with a C(18) column was performed on the oligophenolic fraction, using a novel method developed in this study. RESULTS: Seven fractions were obtained as a function of polarity and molecular weight. Among them, the fraction containing phenolic compounds with a MW ≥ 50 kDa appeared to be the most active, correlated with the content of phenolic compounds. CONCLUSION: This work constitutes a step forward in the separation and purification of bioactive phlorotannins and represents a prerequisite for further investigations into their structural characterisation and distribution in A. nodosum.


Subject(s)
Ascophyllum/chemistry , Free Radical Scavengers/chemistry , Phenols/analysis , Benzothiazoles , Biphenyl Compounds/chemistry , Chromans/chemistry , Chromatography, High Pressure Liquid , Magnetic Resonance Spectroscopy , Molecular Weight , Picrates/chemistry , Solvents , Sulfonic Acids
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