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van Kranenburg, R.

Publications and source records attributed to van Kranenburg, R..

3 recordsLinked to original sources

Parageobacillus thermoglucosidasius and the reductive glycine pathway: A journey of Almosts and Maybes.

We aimed to engineer the reductive glycine pathway (rGlyP) in Parageobacillus thermoglucosidasius for synthetic assimilation of formate and methanol via a mixed rational and evolutionary approach. We attempted to obtain glycine or serine auxotrophic strains in P. thermoglucosidasius as a starting point to impose a selective pressure and engineer formate assimilation via the rGlyP. While serine auxotrophy was partially achieved via gene deletion of serA, alternative glycine biosynthesis routes limited its stringency, and glycine auxotrophy could not be obtained due to unsuccessful genome modification. Even though formate supplementation improved the growth of the serA deficient strain, we confirmed that formate was not assimilated into biomass via 13C-labeling experiments. Thus, we hypothesized the increase in growth of the serA deficient mutant was likely due to extra energy provided by formate oxidation, rather than biomass incorporation. We also attempted heterologous overexpression of the C1 module from Moorella thermoacetica, but this did not yield any detectable effect in growth nor formate assimilation. These findings highlight the challenges in rGlyP implementation in non-model organisms, the need for better metabolic annotation in P. thermoglucosidasius, and provide valuable insights for future engineering of synthetic C1 metabolism in thermophiles via the rGlyP.

bioengineering↗

Awakening of the RuMP cycle for synthetic methylotrophy in the thermophile Parageobacillus thermoglucosidasius.

Given sustainability and scalability concerns of using sugar feedstocks for microbial bioproduction of bulk chemicals, widening the feedstock range for microbial cell factories is of high interest. Methanol is a one-carbon alcohol that stands out as an alternative feedstock for the bioproduction of chemicals, as it is electron-rich, water-miscible and can be produced from several renewable resources. Bioconversion of methanol into products under thermophilic conditions (>50{degrees}C) could be highly advantageous for industrial biotechnology. Although progress is being made with natural, thermophilic methylotrophic microorganisms, they are not yet optimal for bioproduction and establishing alternative thermophilic methylotrophic bioproduction platforms can widen possibilities. Hence, we set out to implement synthetic methanol assimilation in the emerging thermophilic model organism Parageobacillus thermoglucosidasius. We engineered P. thermoglucosidasius to be strictly dependent for its growth on methanol assimilation via the core of the highly efficient ribulose monophosphate (RuMP) cycle, while co-assimilating ribose. Surprisingly, this did not require heterologous expression of RuMP enzymes. Instead, by laboratory evolution we awakened latent, native enzyme activities to form the core of the RuMP cycle. We obtained fast methylotrophic growth in which [~]17% of biomass was strictly obtained from methanol. This work lays the foundation for developing a versatile thermophilic bioproduction platform based on renewable methanol.

synthetic biology↗

Characterizing a thermostable Cas9 for bacterial genome editing and silencing

CRISPR-Cas9 based genome engineering tools have revolutionized fundamental research and biotechnological exploitation of both eukaryotes and prokaryotes. However, the mesophilic nature of the established Cas9 systems does not allow for applications that require enhanced stability, including engineering at elevated temperatures. Here, we identify and characterize ThermoCas9: an RNA-guided DNA-endonuclease from the thermophilic bacterium Geobacillus thermodenitrificans T12. We show that ThermoCas9 is active in vitro between 20{degrees}C and 70{degrees}C, a temperature range much broader than that of the currently used Cas9 orthologues. Additionally, we demonstrate that ThermoCas9 activity at elevated temperatures is strongly associated with the structure of the employed sgRNA. Subsequently, we develop ThermoCas9-based engineering tools for gene deletion and transcriptional silencing at 55{degrees}C in Bacillus smithii and for gene deletion at 37{degrees}C in Pseudomonas putida. Altogether, our findings provide fundamental insights into a thermophilic CRISPR-Cas family member and establish the first Cas9-based bacterial genome editing and silencing tool with a broad temperature range.

microbiology↗