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Coastal herbivorous fishes consume macroalgae, which is then degraded by microbes along their digestive tract. However, there is scarce genomic information about the microbiota that perform this degradation. This study explores the potential of Kyphosus gastrointestinal microbial symbionts to collaboratively degrade and ferment polysaccharides from red, green, and brown macroalgae through in silico study of carbohydrate-active enzyme and sulfatase sequences. Recovery of metagenome-assembled genomes (MAGs) from previously described Kyphosus gut metagenomes and newly sequenced bioreactor enrichments reveals differences in enzymatic capabilities between the major microbial taxa in Kyphosus guts. The most versatile of the recovered MAGs were from the Bacteroidota phylum, whose MAGs house enzyme collections able to decompose a variety of algal polysaccharides. Unique enzymes and predicted degradative capacities of genomes from the Bacillota (genus Vallitalea) and Verrucomicrobiota (order Kiritimatiellales) highlight the importance of metabolic contributions from multiple phyla to broaden polysaccharide degradation capabilities. Few genomes contain the required enzymes to fully degrade any complex sulfated algal polysaccharide alone. The distribution of suitable enzymes between MAGs originating from different taxa, along with the widespread detection of signal peptides in candidate enzymes, is consistent with cooperative extracellular degradation of these carbohydrates. This study leverages genomic evidence to reveal an untapped diversity at the enzyme and strain level among Kyphosus symbionts and their contributions to macroalgae decomposition. Bioreactor enrichments provide a genomic foundation for degradative and fermentative processes central to translating the knowledge gained from this system to the aquaculture and bioenergy sectors.IMPORTANCESeaweed has long been considered a promising source of sustainable biomass for bioenergy and aquaculture feed, but scalable industrial methods for decomposing terrestrial compounds can struggle to break down seaweed polysaccharides efficiently due to their unique sulfated structures. Fish of the genus Kyphosus feed on seaweed by leveraging gastrointestinal bacteria to degrade algal polysaccharides into simple sugars. This study reconstructs metagenome-assembled genomes for these gastrointestinal bacteria to enhance our understanding of herbivorous fish digestion and fermentation of algal sugars. Investigations at the gene level identify Kyphosus guts as an untapped source of seaweed-degrading enzymes ripe for further characterization. These discoveries set the stage for future work incorporating marine enzymes and microbial communities in the industrial degradation of algal polysaccharides.

Marine herbivorous fish that feed primarily on macroalgae, such as those from the genus Kyphosus, are essential for maintaining coral health and abundance on tropical reefs. Here, deep metagenomic sequencing and assembly of gut compartment-specific samples from three sympatric, macroalgivorous Hawaiian kyphosid species have been used to connect host gut microbial taxa with predicted protein functional capacities likely to contribute to efficient macroalgal digestion. Bacterial community compositions, algal dietary sources, and predicted enzyme functionalities were analyzed in parallel for 16 metagenomes spanning the mid- and hindgut digestive regions of wild-caught fishes. Gene colocalization patterns of expanded carbohydrate (CAZy) and sulfatase (SulfAtlas) digestive enzyme families on assembled contigs were used to identify likely polysaccharide utilization locus associations and to visualize potential cooperative networks of extracellularly exported proteins targeting complex sulfated polysaccharides. These insights into the gut microbiota of herbivorous marine fish and their functional capabilities improve our understanding of the enzymes and microorganisms involved in digesting complex macroalgal sulfated polysaccharides. IMPORTANCE This work connects specific uncultured bacterial taxa with distinct polysaccharide digestion capabilities lacking in their marine vertebrate hosts, providing fresh insights into poorly understood processes for deconstructing complex sulfated polysaccharides and potential evolutionary mechanisms for microbial acquisition of expanded macroalgal utilization gene functions. Several thousand new marine-specific candidate enzyme sequences for polysaccharide utilization have been identified. These data provide foundational resources for future investigations into suppression of coral reef macroalgal overgrowth, fish host physiology, the use of macroalgal feedstocks in terrestrial and aquaculture animal feeds, and the bioconversion of macroalgae biomass into value-added commercial fuel and chemical products.

Saccharina latissima is a perennial kelp with a circumboreal distribution from the North Pacific to the North Atlantic coasts. Our study clarified the taxonomy of the morphologically distinct Saccharina latissima forma angustissima (Collins) A.Mathieson from the low intertidal zone on exposed islands and ledges of Casco Bay, Maine, USA. To identify genetic divergence between the two morphotypes, S. latissima and S. latissima f. angustissima, we used a multilocus phylogenetic approach including nuclear-encoded internal transcribed spacer, mitochondrial cox1 and cox3, and plastidencoded rbcL gene sequences. Genetic analysis of the individual markers and combined data set using SVDquartets resulted in p-distance values for all markers of , 1%, suggesting low divergence between the two forms. However, there was as much or more genetic divergence between S. latissima and S. latissima f. angustissima as there were between other taxonomically accepted species of Saccharina. To investigate sexual compatibility between the two forms, we made reciprocal crosses of the gametophytes and observed sporophyte formation. All crosses were successfully grown to the juvenile sporophyte stage, suggesting that the two are reproductively compatible in vitro. It is unknown if the two populations freely hybridize in the field. Last, we compared wave action, the ecological factor most likely driving the unique morphology, at exposed sites with S. latissima f. angustissima and protected sites with S. latissima. The mean wave force at the exposed site was over 30 times higher in magnitude than at the protected site at 160.04 6 32.58 N and 4.75 6 6.75 N, respectively, during the summer. The significant differences in morphology, the lack of specimens with intermediate morphologies, and the results of a common garden experiment suggest that the morphological differences in S. latissima f. angustissima are heritable with a genetic basis. Therefore, on the basis of our molecular evidence coupled with ecological studies, we are elevating S. latissima f. angustissima (Collins) A.Mathieson to specific rank as S. angustissima (Collins) Augyte, Yarish & Neefus comb. nov. & stat. nov. [ABSTRACT FROM AUTHOR]