A review of the microbial production of bioactive natural products and biologics
JV Pham, MA Yilma, A Feliz, MT Majid… - Frontiers in …, 2019 - frontiersin.org
A variety of organisms, such as bacteria, fungi, and plants, produce secondary metabolites,
also known as natural products. Natural products have been a prolific source and an …
also known as natural products. Natural products have been a prolific source and an …
Natural product discovery: past, present, and future
L Katz, RH Baltz - Journal of Industrial Microbiology and …, 2016 - academic.oup.com
Microorganisms have provided abundant sources of natural products which have been
developed as commercial products for human medicine, animal health, and plant crop …
developed as commercial products for human medicine, animal health, and plant crop …
Multigene editing in the Escherichia coli genome via the CRISPR-Cas9 system
Y Jiang, B Chen, C Duan, B Sun, J Yang… - Applied and …, 2015 - Am Soc Microbiol
An efficient genome-scale editing tool is required for construction of industrially useful
microbes. We describe a targeted, continual multigene editing strategy that was applied to …
microbes. We describe a targeted, continual multigene editing strategy that was applied to …
Ketones from aldehydes via alkyl C(sp3)−H functionalization under photoredox cooperative NHC/palladium catalysis
HY Wang, XH Wang, BA Zhou, CL Zhang… - Nature …, 2023 - nature.com
Direct synthesis of ketones from aldehydes features high atom-and step-economy. Yet, the
coupling of aldehydes with unactivated alkyl C (sp3)-H remains challenging. Herein, we …
coupling of aldehydes with unactivated alkyl C (sp3)-H remains challenging. Herein, we …
Evolution and diversity of assembly-line polyketide synthases: Focus review
Assembly-line polyketide synthases (PKSs) are among the most complex protein
machineries known in nature, responsible for the biosynthesis of numerous compounds …
machineries known in nature, responsible for the biosynthesis of numerous compounds …
Opportunities for natural products in 21 st century antibiotic discovery
GD Wright - Natural product reports, 2017 - pubs.rsc.org
Natural products and their derivatives are mainstays of our antibiotic drugs, but they are
increasingly in peril. The combination of widespread multidrug resistance in once …
increasingly in peril. The combination of widespread multidrug resistance in once …
Carbene and photocatalyst-catalyzed decarboxylative radical coupling of carboxylic acids and acyl imidazoles to form ketones
SC Ren, X Yang, B Mondal, C Mou, W Tian… - Nature …, 2022 - nature.com
The carbene and photocatalyst co-catalyzed radical coupling of acyl electrophile and a
radical precursor is emerging as attractive method for ketone synthesis. However, previous …
radical precursor is emerging as attractive method for ketone synthesis. However, previous …
Direct aldehyde C–H arylation and alkylation via the combination of nickel, hydrogen atom transfer, and photoredox catalysis
A mechanism that enables direct aldehyde C–H functionalization has been achieved via the
synergistic merger of photoredox, nickel, and hydrogen atom transfer catalysis. This mild …
synergistic merger of photoredox, nickel, and hydrogen atom transfer catalysis. This mild …
Something old, something new: revisiting natural products in antibiotic drug discovery
GD Wright - Canadian journal of microbiology, 2014 - cdnsciencepub.com
Antibiotic discovery is in crisis. Despite a growing need for new drugs resulting from the
increasing number of multi-antibiotic-resistant pathogens, there have been only a handful of …
increasing number of multi-antibiotic-resistant pathogens, there have been only a handful of …
The influence of natural products upon drug discovery
DJ Newman, GM Cragg, KM Snader - Natural product reports, 2000 - pubs.rsc.org
3 Role of natural products in treatment of diseases 4 Antiinfective agents (including
antimalarials) 4.1 Antibacterials: b-lactams 4.2 Antibacterials: aminoglycosides 4.3 …
antimalarials) 4.1 Antibacterials: b-lactams 4.2 Antibacterials: aminoglycosides 4.3 …