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Brewer, S. L.

Publications and source records attributed to Brewer, S. L..

2 recordsLinked to original sources

DISCOVERY AND BIOCHEMICAL CHARACTERIZATION OF A FUNGAL ICE NUCLEATION PROTEIN FROM PODILA CLONOCYSTIS

Biological ice nucleation plays a pivotal role in atmospheric processes, yet the molecular basis of fungal ice nucleation remains poorly understood compared to bacterial systems. Here, we report the biochemical characterization of an ice nucleation protein (PcINP) from a soil-dwelling fungus Podila clonocystis, not previously reported to produce ice nuclei. Using sequence similarity network analysis, we identified PcINP as a putative fungal homolog of bacterial ice nucleation proteins and confirmed its function through recombinant expression in Escherichia coli. We probe the function of PcINP structure through domain truncations and demonstrate that a poorly structured N-terminal region is not necessary for ice nucleation activity and can be functionally replaced with an expression enhancing SUMO fusion tag. Finally, we observe both monomeric and aggregated PcINP in E. coli lysates using SEC-MALS but are unable to distinguish their ice nucleation activity pointing to an unknown in vitro aggregation mechanism. Our findings establish PcINP within the emerging class fungal ice nucleation protein with distinct structural features and high stability, expanding the known diversity of biological ice nucleators and highlighting their potential for environmental and biotechnological applications.

biochemistry↗

Outer membrane vesicles can contribute to cellulose degradation in Teredinibacter turnerae, a cultivable intracellular endosymbiont of shipworms

Teredinibacter turnerae is a cultivable cellulolytic Gammaproteobacterium (Cellvibrionaceae) that commonly occurs as an intracellular endosymbiont in the gills of wood-eating bivalves of the family Teredinidae (shipworms). The genome of T. turnerae encodes a broad range of enzymes that deconstruct cellulose, hemicellulose, and pectin and contribute to wood (lignocellulose) digestion in the shipworm gut. However, the mechanisms by which T. turnerae secretes lignocellulolytic enzymes are incompletely understood. Here, we show that T. turnerae cultures grown on carboxymethyl cellulose (CMC) produce membrane vesicles (MVs) that include a variety of proteins identified by LC-MS/MS as carbohydrate-active enzymes (CAZymes) with predicted activities against cellulose, hemicellulose, and pectin. Reducing sugar assays and zymography confirm that these MVs exhibit cellulolytic activity, as evidenced by the hydrolysis of CMC. Additionally, these MVs were enriched with TonB-dependent receptors, which are essential to carbohydrate and iron acquisition by free-living bacteria. These observations indicate a potential role for MVs in lignocellulose utilization by T. turnerae in the free-living state, suggest possible mechanisms for host-symbiont interaction, and may be informative for commercial applications such as enzyme production and lignocellulosic biomass conversion.

microbiology↗