Is it time for artificial intelligence to predict the function of natural products based on 2D-structure
One of chemistry's grand challenges is to find a function for every known metabolite. We explore the opportunity for artificial intelligence to provide rationale interrogation of metabolites to predict their function.
Diversification of polyketide structures via synthase engineering
We present examples of polyketide structure diversification along with a perspective on the present and future of polyketide synthetic biology.
Leveraging synthetic biology for producing bioactive polyketides and non-ribosomal peptides in bacterial heterologous hosts
A review discussing the role of heterologous expression in the discovery and engineered production of bioactive polyketides and non-ribosomal peptides from bacteria.
Using Drosophila as a platform for drug discovery from natural products in Parkinson's disease
The review provides an overview of discovery of new drug leads from natural extracts using Drosophila as a screening platform to evaluate the therapeutic potential of phytochemicals against Parkinson's disease.
3-Ketoacyl-ACP synthase (KAS) III homologues and their roles in natural product biosynthesis
KAS III-like enzymes play a significant role in natural product biosynthesis through C–C, C–O, and/or C–N bond formation.
Recent advances in the genome mining of Aspergillus secondary metabolites (covering 2012–2018)
This review covers advances made in genome mining SMs produced by Aspergillus nidulans, Aspergillus fumigatus, Aspergillus niger, and Aspergillus terreus in the past six years (2012–2018). Genetic identification and molecular characterization of SM biosynthetic gene clusters, along with proposed biosynthetic pathways, is discussed in depth.
Synthesis of N-acyl amide natural products using a versatile adenylating biocatalyst
TamA is the enzyme that controls the acyl chain length of the tambjamine natural products. Here we show that the catalytic ANL domain of TamA can be used to prepare a range of N-acyl amides.
The Winding Road of the Uvaretin Class of Natural Products: From Total Synthesis to Bioactive Agent Discovery.
Nodulisporic acid E biosynthesis: in vivo characterisation of NodD1, an indole-diterpene prenyltransferase that acts on an emindole SB derived indole-diterpene scaffold
Prenylation of aromatic compounds is a key tailoring reaction in biosynthesis of bioactive indole-diterpenes.
Fungal natural alkaloid schizocommunin activates the aryl hydrocarbon receptor pathway
Activation of AhR by schizocommunin is linked to increased expression of xenobiotic metabolizing enzymes associated with immune and allergic responses.
Synthesis, conformational preferences, and biological activity of conformational analogues of the microtubule-stabilizing agents, (−)-zampanolide and (−)-dactylolide
Zampanolide and dactylolide are microtubule-stabilizing polyketides possessing potent cytotoxicity towards a variety of cancer cell lines.
How mithramycin stereochemistry dictates its structure and DNA binding function
The crystal structures of mithramycin and its analogue reveal how the chemistry of mithramycin shapes it for DNA binding.
Volatiles from the ascomycete Daldinia cf. childiae (Hypoxylaceae), originating from China
The volatiles from an isolate of the fungus Daldinia cf. childiae, obtained from a specimen collected in China, were collected by use of a closed-loop stripping apparatus and analysed by GC-MS.
Synthesis of endolides A and B: naturally occurring N-methylated cyclic tetrapeptides
The first syntheses of the bioactive cyclic tetrapeptide natural products, endolides A and B, were accomplished using a solution-phase macrocyclisation reaction; the stereoselectivity of which was found to be reagent-controlled.
Construction of a hybrid gene cluster to reveal coupled ring formation–hydroxylation in the biosynthesis of HSAF and analogues from Lysobacter enzymogenes
HSAF and analogues are polycyclic tetramate macrolactams (PoTeMs) isolated from Lysobacter enzymogenes.
Synthesis and Direct Comparison of the Anticancer Activities of Phomopsolides D/E and Two 7-Oxa-/7-Aza-analogues
Stereoselective semi-synthesis of the neuroprotective natural product, serofendic acid
Our synthesis of neuroprotectant serofendic acid from biosourced ent-atis-16-en-19-oic acid represents the best route to date.
Origin and bioactivities of thiosulfinated FK228
During a large laboratory-scale purification of FK228 from the fermentation broth of Burkholderia thailandensis MSMB43, a small amount of thiosulfinated FK228 (TS-FK228) was unexpectedly purified only after the broth was mixed with silica gel.
Isolation and characterization of tambjamine MYP1, a macrocyclic tambjamine analogue from marine bacterium Pseudoalteromonas citrea
Identification of a macrocyclic tambjamine natural product, tambjamine MYP1, from a marine bacterium that may enhance bioactivity by restraining bond rotation.