These findings provide new insights into the genomic basis of ecological adaptation and metabolic diversification in Pseudoalteromonas, supporting the role of pigmentation as a proxy for enhanced biosynthetic potential, while carbohydrate utilization capabilities evolve more independently and offering a framework for targeted bioprospecting of marine-derived metabolites with industrial and environmental applications.
Abstract
Pseudoalteromonas species are ecologically versatile marine bacteria widely recognized for their capacity to synthesize diverse bioactive metabolites and psychrophilic enzymes with biotechnological relevance. Here, we present a comprehensive comparative genomic analysis of 53 reference genomes to elucidate the dynamics, functional diversity, and biosynthetic potential of this genus. Reference genomes representing each deposited species were selected in order to avoid bias associated with unequal numbers of genomes per species. Pangenome reconstruction revealed an open structure comprising a small core genome (1,350 gene families) and a large proportion of accessory and strain-specific genes, reflecting extensive genomic plasticity. Functional annotation indicated that accessory regions are enriched for genes involved in secondary metabolism, stress adaptation, and environmental resilience. Notably, biosynthetic gene cluster (BGC) mining uncovered a rich repertoire of potentially novel RiPPs and other secondary metabolite clusters, underscoring Pseudoalteromonas as a promising source of unexplored bioactive compounds. Statistical analyses revealed that pigmented strains harbor significantly higher numbers of BGCs compared to non-pigmented strains, while only a weak and non-significant correlation was observed between BGC abundance and carbohydrate-active enzyme (CAZyme) content. No significant effect of the isolation source was detected on either BGC or CAZyme distributions. Together, these findings provide new insights into the genomic basis of ecological adaptation and metabolic diversification in Pseudoalteromonas, supporting the role of pigmentation as a proxy for enhanced biosynthetic potential, while carbohydrate utilization capabilities evolve more independently and offering a framework for targeted bioprospecting of marine-derived metabolites with industrial and environmental applications.
Conordance of codon usage and functional gene abundance with phylogeny is revealed, along with diverse host- and lifestyle-associated adaptive strategies in this important group of plant pathogens.
Jian-Xin Shen, M. Qiao, Jiahao Hong et al.· IMA Fungus· 0 citations
A genomic framework for understanding the high glycosphingolipid-producing capacity of NKG400013 is established and insights into the evolutionary diversification of sphingolipid metabolism in green algae are provided.
Rein Yasui, Aoi Hosaka, N. Ogata et al.· DNA Research· 0 citations
The findings reveal S. rubidaea MJ24 as a metabolically versatile bacterium with a rich secondary metabolite repertoire and significant agricultural and biotechnological promise.
Yaseera N. Bhombal, Surabhi Yeole, V. Barvkar et al.· Functional & Integrative Gen...· 0 citations
Aquirufa
is a widespread and diverse bacterial genus inhabiting freshwater ecosystems. Analyses of genomes from cultured strains and metagenome-assembled genomes (MAGs) of the genus revealed four phylogenetically distinct branches that differed markedly in the proportions of cultured strains and MAGs they contained. In total, 56 species or species-like taxa were identified, including eight novel species described here. Proteorhodopsin genes were detected in many of the genomes and were found across a wide range of habitat types, but their prevalence differed considerably among the four phylogenetic branches. Detailed analyses of two branches with markedly different proteorhodopsin gene frequencies suggested differences in the occurrence, size, structure, and pangenomes of their populations. Comparative whole-genome analyses showed that proteorhodopsin genes in
Aquirufa
consistently co-occurred with two key genes involved in retinal chromophore biosynthesis. These three genes exhibited distinct evolutionary patterns, most likely reflecting differences in recombination and co-evolution. Phylogenetic analyses placed the
Aquirufa
proteorhodopsins within the proteorhodopsin-xanthorhodopsin clade, specifically in a lineage comprising proteorhodopsins from species of the phylum
Bacteroidota
. Extending the analyses to related proteorhodopsins revealed additional patterns. Thirteen distinct gene arrangement types and all three common spectral-tuning residues were identified, with variation occurring not only among genera but occasionally even among species within the same genus. Overall, our findings indicated that the evolution, acquisition, horizontal transfer, and recombination of proteorhodopsin genes and associated genes have proceeded differently across taxonomic groups.
Alexandra Pitt, Stefan Lienbacher, J. Schmidt et al.· Microbial Ecology· 0 citations