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Two review papers, eight research articles, and one brief report were published in this Special Issue. They showed the rich resources that are present within the genomes of marine microorganisms and discussed the use of recently developed tools and technologies to exploit this genetic richness. Examples include the rational supply of precursors according to the relevant biosynthetic pathway and stress driven discovery together with the use of histone deacetylase inhibitors to facilitate the discovery of new bioactive molecules with potential biopharmaceutical applications. We believe that the content of this Special Issue reflects the current state-of-the-art research in this area and highlights the interesting strategies that are being employed to uncover increasing numbers of exciting novel compounds for drug discovery from marine genetic resources.
Stachybotrys --- isoindolinone biosynthesis --- genome mining --- amino compound --- fibrinolytic activity --- antimicrobial --- marine natural products (MNPs) --- secondary metabolites --- antibacterial --- antifungal --- genome mining --- sponge --- meroterpenoid --- marine natural product --- medicinal chemistry --- biosynthesis --- drug discovery --- bacillibactin --- bacillomycin --- genome mining --- marine Bacillus --- nonribosomal peptides --- marine microorganisms --- Streptomyces pratensis --- polyketide antibiotics --- metal stress technique --- antimicrobial activity --- halo-extremophyles --- archaea --- 16S rRNA metagenomics --- haloenzymes --- Odiel marshlands --- Penicillium chrysogenum --- secondary metabolites --- histone-deacetylase inhibitor --- antibacterial activity --- polyketide synthase --- NdgRyo --- IclR family regulator --- Streptomyces --- fatty acid amide --- genome mining --- Marisediminicola --- Antarctica --- carotenoid --- actinobacteria --- natural products --- gene cluster --- Streptomyces --- comparative genomics --- secondary metabolites --- biosynthetic gene clusters --- phylotype --- ecotype --- Streptomyces sp. SCSIO 40010 --- marine --- genome mining --- polycyclic tetramate macrolactams --- cytotoxicity
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Marine natural products containing a heterocyclic moiety in their structure are present in a wide variety of sponges, corals, algae, and fungi. Many of them show important biological activities such as cytotoxic properties against several cancer cell lines. Their challenging chemical structures have attracted the attention of many researchers who have developed various synthetic approaches. This Special Issue presents some examples of new synthetic or biosynthetic methodologies to access this type of marine natural drug.
smenamides --- marine natural products --- peptide/polyketide molecules --- synthetic analogues --- functional-analogues --- antiproliferative activity --- MM cell line --- alotamide --- asymmetric synthesis --- relative structural determination --- tetrahydropyrans --- acid mediated cyclization --- stereoselective --- marine drugs analogues --- pallescensin 1 --- pallescensin 2 --- dihydropallescensin 2 --- isomicrocionin-3 --- pallescensone --- furanosesquiterpenes --- stereoselective synthesis --- lipase-mediated resolution --- cyclogeranylsulfonylbenzene isomers --- microalgae --- Synechococcus sp. PCC 7942 --- short chain fatty acids --- ?-ketoacyl ACP Synthase --- psammaplin A --- marine natural product --- biological activity --- structural modification --- benzo[d]thiazol --- synthesis --- antarctic-derived fungus --- antidepressant --- anticonvulsant --- toluquinol --- thymoquinone --- marine hydroquinone --- antitumor --- natural compound analogues --- hybrid polyketides --- tetramic acid --- Cladosporium sphaerospermum --- hybrid PKS-NRPS --- LLC-PK1 cells --- GGPPS --- Haematococcus pluvialis --- astaxanthin --- Iso-Seq --- anticandidal activity --- antimicrobial peptides --- Candida albicans --- Octominin --- Octopus minor
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