Biology subjects

Puiggene, O.

Publications and source records attributed to Puiggene, O..

3 recordsLinked to original sources

bioRxiv2025

Co-Substrate Free Valorisation of Lignin Monomers by Assimilation of C1 and C2 By-Products

Lignin is an underutilised global resource with significant potential for the production of chemicals that are currently derived from fossil resources. However, biotechnological lignin valorisation faces various challenges including its recalcitrance and the toxicity of aromatic intermediates, products, and by-products like formaldehyde. While biochemical production from lignin-derived monomers has been demonstrated by disrupting native lignin degradation pathways, this approach required co-feeding additional carbon sources such as glucose for growth. This dependence on additional carbon sources can create competition with the food industry and undermine the economic sustainability of the bioprocess. Here, we report growth of a protocatechuate production strain of Pseudomonas putida EM42 on the by-products from p-coumarate and ferulate valorisation, achieving carbon efficiencies of up to 78 %. Additional flux balance analysis identified C1 assimilation pathways, including two novel pathways, beneficial for the growth on the formaldehyde by-product from ferulate degradation leading to improved carbon utilisation. This study demonstrates how by-product utilisation from lignin conversion can eliminate the need for co-feeding additional carbon sources, thereby potentially improving the efficiency of lignin valorisation.

bioengineering↗

bioRxiv2025

Systematic engineering of synthetic serine cycles in Pseudomonas putida uncovers emergent topologies for methanol assimilation

The urgent need for a circular carbon economy has driven research into sustainable substrates, including one-carbon (C1) compounds. The non-pathogenic soil bacterium Pseudomonas putida is a promising host for exploring synthetic methylotrophy due to its versatile metabolism. In this work, we implemented synthetic serine cycle variants in P. putida for methanol assimilation combining modular engineering and growth-coupled selection, whereby methanol assimilation supported biosynthesis of the essential amino acid serine. The serine cycle forms acetyl-coenzyme A from C1 molecules without carbon loss but has bottlenecks that hinder engineering efforts. We adopted three synthetic variants (serine-threonine cycle, homoserine cycle, and modified serine cycle) that yield serine in a methanol-dependent fashion to overcome these challenges. By dividing these metabolic designs into functional modules, we systematically compared their performance for implementation in vivo. Additionally, we harnessed native pyrroloquinoline quinone-dependent dehydrogenases for engineering methylotrophy. Recursive rewiring of synthetic and native activities revealed novel metabolic topologies for methanol utilization, termed enhanced serine-threonine cycle, providing a blueprint for engineering C1 assimilation in non-model heterotrophic bacteria. GRAPHICAL ABSTRACT O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=168 SRC="FIGDIR/small/638773v1_ufig1.gif" ALT="Figure 1"> View larger version (79K): org.highwire.dtl.DTLVardef@1bfccd0org.highwire.dtl.DTLVardef@11f77deorg.highwire.dtl.DTLVardef@f6a904org.highwire.dtl.DTLVardef@1d24a34_HPS_FORMAT_FIGEXP M_FIG C_FIG

synthetic biology↗

bioRxiv2024

Growth-coupled microbial biosynthesis of the animal pigment xanthommatin

The mining of genomes across life has unearthed a bounty of biosynthetic potential to diverse molecules key to a biobased future. While the heterologous expression of metabolic pathways has achieved broad success, most approaches suffer a similar fate in low initial production levels that require extensive, resource-heavy iterative strain engineering refinement. Herein we introduce a growth-coupled biosynthetic (GrowBio) strategy that irrevocably connects microbial growth with specialized compound production. We demonstrate the plug-and-play versatility of GrowBio in the production of the structurally complex animal biopigment xanthommatin, a color-changing ommochrome with material and cosmetic potential. Xanthommatin biosynthesis directly fuels growth of a newly designed Pseudomonas putida 5,10-methylenetetrahydrofolate auxotroph (PUMA). Aided by genome-scale metabolic modeling, PUMA was designed and built to be controlled by endogenous formate co-produced as a coupled biosynthetic byproduct in the multistep conversion of tryptophan to xanthommatin. Adaptive laboratory evolution was utilized to streamline xanthommatins gram-scale bioproduction via growth rate selection, establishing GrowBio as a promising biotechnological approach for establishing and optimizing the microbial production of value-added molecules.

synthetic biology↗