Publications by authors named "G Sabat"

The soil environment affected by plant roots and their exudates, termed the rhizosphere, significantly impacts crop health and is an attractive target for engineering desirable agricultural traits. Engineering microbes in the rhizosphere is one approach to improving crop yields that directly minimizes the number of genetic modifications made to plants. Soil microbes have the potential to assist with nutrient acquisition, heat tolerance, and drought response if they can persist in the rhizosphere in the correct numbers.

View Article and Find Full Text PDF

Kunitz-type trypsin inhibitors are ubiquitous in plants. They have been proposed to be a part of a defense mechanism against herbivores. Trypsin inhibitors also have potential applications in the biotechnology industry, such as in mammalian cell culture.

View Article and Find Full Text PDF
Article Synopsis
  • Cysteine dioxygenase (CDO) is an enzyme that converts cysteine into cysteine sulfinic acid, with a unique crosslink enhancing its catalytic efficiency.
  • The study focused on creating a variant of bacterial CDO (G82C) to test if a single DNA mutation could allow crosslink formation, showing that it indeed can form the crosslink but with lower efficiency than the wild-type enzyme.
  • Bioinformatics revealed many potential crosslinked CDOs in Gram-negative pathogenic bacteria, indicating a broader biological significance for this crosslink formation.
View Article and Find Full Text PDF

The brown rot fungus Fomitopsis pinicola efficiently depolymerizes wood cellulose via the combined activities of oxidative and hydrolytic enzymes. Mass spectrometric analyses of culture filtrates identified specific proteins, many of which were differentially regulated in response to substrate composition.

View Article and Find Full Text PDF

Mapping networks of RNA-protein interactions in cells is essential for understanding the inner workings of many biological processes, including RNA processing, trafficking, and translation. Current methods for studying protein-RNA interactions rely mostly on purification of poly(A) transcripts, which represent only ~2-3% of total RNAs (). Alternate robust methods for tagging RNA molecules with an RNA aptamer (, MS2-, U1A- and biotin-RNA aptamer) and capturing the RNA-protein complex by the respective aptamer-specific partner are not extensively studied.

View Article and Find Full Text PDF