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Geiger, O.

Publications and source records attributed to Geiger, O..

3 recordsLinked to original sources

Genes required for the formation of virulence-provoking bacterial sphingolipids

Sphingolipids are ubiquitous in membranes of eukaryotes and are associated with important cellular functions. Although sphingolipids occur scarcely in bacteria, for some of them they are essential and, in other bacteria, they contribute to fitness and stability of the outer membrane, such as in the well-studied -proteobacterium Caulobacter crescentus. We previously defined five structural genes for ceramide synthesis in C. crescentus. However, other mutants affected in genes of this same genomic region show cofitness with a mutant deficient in serine palmitoyltransferase. Here we show that at least two phospho-sphingolipids are produced in C. crescentus and that at least another six gene products are needed for the decoration of ceramide upon phospho-sphingolipid formation. All eleven genes participating in phospho-sphingolipid formation are also required in C. crescentus for membrane stability and for displaying sensitivity towards the antibiotic polymyxin B. The genes for the formation of complex phospho-sphingolipids are also required for C. crescentus virulence on Galleria mellonella insect larvae. Author SummarySphingolipids participate in the formation of biological membranes and molecular signaling in higher organisms. Many bacteria also accommodate sphingolipids in their membranes. Here we report that eleven genes participate in the synthesis of complex bacterial phospho-sphingolipids. Our data show that these lipids contribute to membrane stability, but also confer sensitivity towards certain antibiotics. The bacterium Caulobacter crescentus is widely distributed in fresh water lakes and streams and was considered to be non-virulent. However, we demonstrate that complex phospho-sphingolipids are the main virulence contributors in this bacterium.

microbiology↗

Formation of sulfoquinovosyl diacylglycerol by acylation of sulfoquinovosyl glycerol

Sulfoquinovosyl diacylglycerol (SQDG) is a membrane-forming lipid present in photosynthetic organisms as well as in distinct bacteria growing in phosphate-limited environments. Four genes for SQDG biosynthesis were previously identified in Rhodobacter sphaeroides, the operon sqdBDC and sqdA. In this work, we found that SMc02490 of Sinorhizobium meliloti is an SqdA orthologue. Expression of the S. meliloti sqdBDC operon in Escherichia coli results in formation of sulfoquinovosyl glycerol (SQGro), while co-expression of this operon together with smc02490 (sqdA) results in formation of SQDG. Furthermore, SqdA allows for incorporation of exogenous SQGro into SQDG in S. meliloti and in E. coli cultures, suggesting that presence of SqdA in bacteria permit them to use environmental SQGro for the biosynthesis of the membrane lipid SQDG. An in vitro enzymatic assay for the acyltransferase SqdA was developed. Cell-free crude extracts of E. coli expressing sqdA can efficiently convert [35S]-sulfoquinovosyl monoacylglycerol into SQDG using as acyl donor acyl carrier protein. Bioinformatic analyses reveal that this sulfoquinovose acylation pathway for SQDG biosynthesis is delimited to the Hyphomicrobiales (Rhizobiales) and Rhodobacterales orders of Alphaproteobacteria.

microbiology↗

On the bacterial ancestry of mitochondria: new insights with triangulated approaches

We breathe at the molecular level when mitochondria in our cells consume oxygen to extract energy from nutrients. Mitochondria are characteristic cellular organelles that derive from aerobic bacteria similar to some of those thriving in the oceans nowadays. These organelles carry out most metabolic pathways in eukaryotic cells. The precise bacterial origin of mitochondria and, consequently, the metabolic ancestry of our cells remains controversial - despite the vast genomic information that is now available. Here we triangulate across multiple phylogenomic and molecular approaches to pinpoint the most likely living relatives of the ancestral bacteria from which mitochondria originated.

evolutionary biology↗