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Principal coordinates analysis (PCoA) plots depicting the ordination of archaeal communities in rhizospheric (R) and bulk (S) soils of Moringa oleifera at the phylum ( a ) and genus ( b ) levels, based on Bray–Curtis dissimilarities of <t>metagenomic</t> profiles. Samples cluster according to soil compartment, indicating distinct archaeal community compositions between rhizosphere and bulk soil
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Principal coordinates analysis (PCoA) plots depicting the ordination of archaeal communities in rhizospheric (R) and bulk (S) soils of Moringa oleifera at the phylum ( a ) and genus ( b ) levels, based on Bray–Curtis dissimilarities of <t>metagenomic</t> profiles. Samples cluster according to soil compartment, indicating distinct archaeal community compositions between rhizosphere and bulk soil
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Principal coordinates analysis (PCoA) plots depicting the ordination of archaeal communities in rhizospheric (R) and bulk (S) soils of Moringa oleifera at the phylum ( a ) and genus ( b ) levels, based on Bray–Curtis dissimilarities of metagenomic profiles. Samples cluster according to soil compartment, indicating distinct archaeal community compositions between rhizosphere and bulk soil

Journal: BMC Genomics

Article Title: Functional potential of archaeal KEGG enzymes in the Moringa oleifera rhizosphere revealed by metagenomic analysis

doi: 10.1186/s12864-026-12700-3

Figure Lengend Snippet: Principal coordinates analysis (PCoA) plots depicting the ordination of archaeal communities in rhizospheric (R) and bulk (S) soils of Moringa oleifera at the phylum ( a ) and genus ( b ) levels, based on Bray–Curtis dissimilarities of metagenomic profiles. Samples cluster according to soil compartment, indicating distinct archaeal community compositions between rhizosphere and bulk soil

Article Snippet: All samples were immediately stored at − 20 °C, and total genomic DNA from the soil microbiomes was isolated utilizing the CTAB/SDS extraction protocol and concentrations normalized to 10 ng/μl per established protocols [ ], then 30 μl aliquots of each specimen were dispatched to Novogene Co. (Singapore) for comprehensive metagenomic whole-genome shotgun sequencing analysis.

Techniques: