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Biology subjects

Lengger, B.

Publications and source records attributed to Lengger, B..

2 recordsLinked to original sources

Engineered cell differentiation and sexual reproduction in probiotic and mating yeasts

G protein-coupled receptors (GPCRs) enable cells to sense environmental cues and are indispensable for coordinating vital processes including quorum sensing, proliferation, and sexual reproduction. GPCRs comprise the largest class of cell surface receptors in eukaryotes, and for more than three decades the pheromone-induced mating pathway in bakers yeast Saccharomyces cerevisiae has served as a model for studying heterologous GPCRs (hGPCRs). Here we report transcriptome profiles following mating pathway activation in native and hGPCR-signaling yeast, and use a model-guided approach to correlate gene expression to morphological changes. From this we demonstrate mating between haploid cells armed with hGPCRs and endogenous biosynthesis of their cognate ligands. Furthermore, we devise a ligand-free screening strategy for hGPCR compatibility with the yeast mating pathway and enable hGPCR-signaling in the probiotic yeast Saccharomyces boulardii. Combined, our findings enable new means to study mating, hGPCR-signaling, and cell-cell communication in a model eukaryote and yeast probiotics. One-sentence summaryEnabling sensing in probiotic yeast and synthetic yeast mating with human and fungal G protein-coupled receptors.

cell biology↗

Serotonin GPCR-based biosensing modalities in yeast

Serotonin is a key neurotransmitter involved in numerous physiological processes and serves as an important precursor for manufacturing bioactive indoleamines and alkaloids used in the treatment of human pathologies. In humans, serotonin sensing and signaling can occur by 12 G protein-coupled receptors (GPCRs) coupled to G proteins. To systematically assess serotonin GPCR signaling, we characterized reporter gene expression of a 144-sized library encoding all 12 human serotonin GPCRs in combination with 12 different G proteins in yeast exposed to serotonin. For the 5-HT4 receptor, we observe 25- and 64-fold changes in EC50 values and dynamic reporter gene outputs, respectively. Furthermore, we show that optimal biosensing designs enable high-resolution sensing of serotonin produced in yeast, as well as provide a platform for characterization of 19 serotonin GPCR polymorphisms found in human populations. Taken together, our study highlights serotonin biosensing modalities of relevance to both biotechnological and human health applications. HighlightsO_LIHuman serotonin G protein-coupled receptors display promiscuous G coupling in yeast C_LIO_LIG-coupled serotonin receptors display up to 64-fold changes in reporter expression output C_LIO_LIDifferences in G protein evokes 25- and 2-fold difference in EC50 and sensitivity, respectively C_LIO_LISerotonin receptor 5-HT4 and human SNP variants display physiologically relevant EC50 values in yeast C_LIO_LI5-HT4 can be applied for high-resolution biosensing of serotonin produced from yeast C_LI

bioengineering↗