Abstract:Phomopsischalins A (1) and B (2), two unprecedented cytochalasins featuring a 5/6/6/7-fused tetracyclic ring system, and Phomopsischalin C (3) bearing a 5/6/5/8-fused tetracyclic ring system, were isolated from the endophytic...
“…The genus Diaporthe / Phomopsis showed the potential to produce several cytochalasins [7,12,63] . The cytochalasins are fungal toxins with cell membrane permeability that exhibit structural diversity and several biological effects, such as cytotoxic, anticancer, antimicrobial and antiparasitic activities, inhibition of acetylcholinesterase enzyme in vitro and promotion of lysosomal function [12,64–68] …”
Endophytic fungi are associated with plant health and represent a remarkable source of potential of enzymes and bioactive compounds, but the diversity of endophytes remains uncertain and poorly explored, especially in Cactaceae, one of the most species‐rich families adapted to growing in arid and semi‐arid regions. The aim of this study was to conduct a systematic review on the diversity and bioprospecting of endophytic fungi from Cactaceae. We analysed peer‐reviewed articles from seven databases using PRISMA guidelines. The results showed that the Cactaceae family is a source of new taxa, but the diversity of endophytic fungi of Cactaceae is little explored, mainly the diversity among tissues and by metagenomics. Bioprospecting studies have shown that these microorganisms can be used in the production of enzymes and larvicidal and antifungal compounds. Our results are relevant as a starting point for researchers to develop studies that expand the knowledge of plant mycobiota in arid and semi‐arid ecosystems, as well as comprising a remarkable source of fungal compounds with several biotechnological applications.
“…The genus Diaporthe / Phomopsis showed the potential to produce several cytochalasins [7,12,63] . The cytochalasins are fungal toxins with cell membrane permeability that exhibit structural diversity and several biological effects, such as cytotoxic, anticancer, antimicrobial and antiparasitic activities, inhibition of acetylcholinesterase enzyme in vitro and promotion of lysosomal function [12,64–68] …”
Endophytic fungi are associated with plant health and represent a remarkable source of potential of enzymes and bioactive compounds, but the diversity of endophytes remains uncertain and poorly explored, especially in Cactaceae, one of the most species‐rich families adapted to growing in arid and semi‐arid regions. The aim of this study was to conduct a systematic review on the diversity and bioprospecting of endophytic fungi from Cactaceae. We analysed peer‐reviewed articles from seven databases using PRISMA guidelines. The results showed that the Cactaceae family is a source of new taxa, but the diversity of endophytic fungi of Cactaceae is little explored, mainly the diversity among tissues and by metagenomics. Bioprospecting studies have shown that these microorganisms can be used in the production of enzymes and larvicidal and antifungal compounds. Our results are relevant as a starting point for researchers to develop studies that expand the knowledge of plant mycobiota in arid and semi‐arid ecosystems, as well as comprising a remarkable source of fungal compounds with several biotechnological applications.
“…Conformational analysis of the isolated compounds was carried out with the MMFF94 force field in CONFLEX software. 33,34 All obtained conformers were screened based on the energy of optimized structures at the B3LYP/6-31G(d) level with an energy window of 10 kcal mol −1 using the Gaussian 09 program package. 35 The theoretical ECD calculations of the conformations of compounds were performed with the TDDFT method at the B3LYP/6-311++G(2d,p) level with the CPCM model in methanol solution.…”
Compounds 1a/1b are a pair of enantiomers characterized by an unprecedented 6/5/6/5/6 N,O-heterocyclic scaffold with a unique spiro[4.5] core. Compound 2 is the first 6/5/6/5/5/6 hexacyclic skeleton fused with an unexpected dispiro[4.4.0.4] system.
“…The conformational analysis of 1–6 was conducted using Spartan software with Molecular Merck force field (MMFF94). 39–43 These conformers were optimized at the B3LYP/6-31G(d) level. The optimized conformers were calculated by the TDDFT method at the B3LYP/6-311++G(2d,p) level.…”
Guaiane-type sesquiterpenoids are well-known in medicinal chemistry of natural products, but the unprecedented sesquiterpenoid scaffold furnished by forming unexpected carbon-carbon linkages or occurring startling cracking deserves expected to be further...
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