Publications by authors named "M Perner"

The vaginal microbiome's role in risk, progression, and treatment of female cancers has been widely explored. Yet, there remains a need to develop methods to understand the interaction of microbiome factors with host cells and to characterize their potential therapeutic functions. To address this challenge, we developed a systems biology framework we term the Pharmacobiome for microbiome pharmacology analysis.

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We report a scalable hydrogenation method for nitriles based on cost-effective materials in a very simple two-electrode setup under galvanostatic conditions. All components are commercially and readily available. The method is very easy to conduct and applicable to a variety of nitrile substrates, leading exclusively to primary amine products in yields of up to 89% using an easy work-up protocol.

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Article Synopsis
  • Chemolithoautotrophic Hydrogenovibrio are common at hydrothermal vents and can oxidize sulfur, hydrogen, or iron, although no species are known to utilize all three energy sources.* -
  • Researchers isolated three Hydrogenovibrio strains from the Indian Ridge that can use iron, hydrogen, or thiosulfate, presenting data on their oxidation rates and carbon dioxide fixation.* -
  • The study found significant differences in gene expression based on the electron donor used, revealing potential unknown pathways for iron oxidation despite no recognized iron-oxidation genes being present.*
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Anthropogenic carbon dioxide (CO) levels are rising to alarming concentrations in earth's atmosphere, causing adverse effects and global climate changes. In the last century, innovative research on CO reduction using chemical, photochemical, electrochemical and enzymatic approaches has been addressed. In particular, natural CO conversion serves as a model for many processes and extensive studies on microbes and enzymes regarding redox reactions involving CO have already been conducted.

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We report an enantioselective copper-catalyzed Kinugasa/aldol domino reaction. This strategy enables access to a range of spirocyclic β-lactam pyrrolidinones in a stereoselective fashion. Under mild reaction conditions, prochiral alkyne-tethered ketones are coupled with nitrones to enable the facile construction of two spirofused ring systems containing three continuous stereocenters with excellent enantioselectivity.

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