Staff scientist, MycoSynVac project co-coordinator
I am a biotechnologist and I have been study in for more than 10 years Mycoplasmas. I have always belived that understanding is the basics for rational engineering. Mycoplasmas being the bacteria with smallest genomes are considered the best models to be characterized by Systems Biology approaches. By combining molecular biology, “-omics” techinques and modelling we have acquired the knowledge in the biology of M. pneumoniae. This knowledge opened the door to genome engineering, becoming a lab of design of biological systems. As co-coordinator of MycoSynVac, in our group, I have the privilege of working with a team of 15 scientists with different backgrounds. Altogether, we aim to develop the first bacterial chassis that can be used for different biotechnological applications. Also, the collaborative efforts and multidisciplinary of the consortium will do MycoSynVac true. This project will be the first proof of concept of engineering the chassis to obtain a multivalent vaccine. We envision that this chassis will open the door to the development of Synthetic Biology, the understanding of Biology and the development of science in Europe and worldwide.
Publications
2018. Cryo-electron tomography analyses of terminal organelle mutants suggest the motility mechanism of Mycoplasma genitalium.  Mol Microbiol 108(3):319-329
,2017. Defined chromosome structure in the genome-reduced bacterium Mycoplasma pneumoniae.  Nat Commun 8:14665
,2016. Bacterial antisense RNAs are mainly the product of transcriptional noise.  Sci Adv 2(3):e1501363
,2016. Integration of multi-omics data of a genome-reduced bacterium: Prevalence of post-transcriptional regulation and its correlation with protein abundances.  Nucleic Acids Res 44(3):1192-202
,2016. Rescuing discarded spectra: Full comprehensive analysis of a minimal proteome.  Proteomics 16(4):554-63
,2015. Comparative "-omics" in Mycoplasma pneumoniae Clinical Isolates Reveals Key Virulence Factors.  PLoS One 10(9):e0137354
,2015. Distinguishing between productive and abortive promoters using a random forest classifier in Mycoplasma pneumoniae.  Nucleic Acids Res 43(7):3442-53
,2015. Defining a minimal cell: essentiality of small ORFs and ncRNAs in a genome-reduced bacterium.  Mol Syst Biol 11(1):780
,2015. MyMpn: a database for the systems biology model organism Mycoplasma pneumoniae.  Nucleic Acids Res 43(Database issue):D618-23
,2014. Assessing the hodgepodge of non-mapped reads in bacterial transcriptomes: real or artifactual RNA chimeras?  BMC Genomics 15:633
,2013. In situ overlap and sequence synthesis during DNA assembly.  ACS Synth Biol 2(12):750-5
,2013. Dissecting the energy metabolism in Mycoplasma pneumoniae through genome-scale metabolic modeling.  Mol Syst Biol 9:653
,2013. Comprehensive methylome characterization of Mycoplasma genitalium and Mycoplasma pneumoniae at single-base resolution.  PLoS Genet 9(1):e1003191
,2012. Transcription start site associated RNAs in bacteria.  Mol Syst Biol 8:585
,2011. A trigger enzyme in Mycoplasma pneumoniae: impact of the glycerophosphodiesterase GlpQ on virulence and gene expression.  PLoS Pathog 7(9):e1002263
,2011. Bacterial transcriptomics: what is beyond the RNA horiz-ome?  Nat Rev Microbiol 9(9):658-69
,2010. Cell division in a minimal bacterium in the absence of ftsZ.  Mol Microbiol 78(2):278-89
,2007. A new promoterless reporter vector reveals antisense transcription in Mycoplasma genitalium.  Microbiology 153(Pt 8):2743-52
,Publication list retrieved from NCBI using ImpactPubs
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