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This abstract was last modified on April 2, 2024 at 5:11 a.m..

University of Ibadan
Corresponding Faculty Member: Olubusuyi Moses Adewumi, adewumi1@hotmail.com
This abstract WILL be considered for a talk.
Complete Genome Sequence Annotation of Arthrobacter Bacteriophage Mudpuppy
Emmanuel O Adebayo, Saheed Adedokun, Adesubomi A Adegbite, Oyindamola A Adegoke, Aisha O Adeniyi, Ridwan A Agboola, Mabel P Aruwajoye, Valentina R Atayero, Warith A Azeez, Damilola Bakare, Oyindamola M Balogun, Ruqayyah A Bello, Abuoma E Ejikeme, Marufat O Hassan, Joseph A Odjirigho, Peace O Okunade, Oluwaseyi J Okunade, Oluwadare O Owolabi, Muideen Raifu, Ini Adebiyi, Veronica I Ogunleye, Temitope O Faleye, Adeleye S Bakarey, Olubusuyi M Adewumi, John I Anetor, Olusegun G Ademowo

Arthrobacter bacteriophage Mudpuppy was originally isolated by University of Ottawa, Canada in 2021. The bacteriophage has a linear genome with 3’ sticky overhang of 11 bases, and was isolated on Arthrobacter globiformis NRRL B-2880 host. It has a genome length of 43,824 base pairs, an approximate shotgun coverage of 1582X and GC content of 67.6%. Whole genome sequence alignment carried out on NCBI-Blastn and Phagesdb.org reveals high nucleotide sequence identity with other phages belonging to cluster AZ. Auto-annotation was carried out using Glimmer and Genemark in-built gene predictors in DNA Master and RAST server and both predicted 70 gene features. Manual inspection and start site refinement using conserved start site predictions from Starterator index, gene synteny on Phamerator and six-frame translation inspection on DNA Master and Artemis Comparison Tool. Assignment of putative functions was done on NCBI protein Blast, HHPred databases, while phylogenetic nucleotide identity of the cluster was generated using the Orthologous Average Nucleotide Identity Tool. The genome structural organization comprised of 95% forward transcribed genes and 5% reverse-transcribed genes, out of the seventy validated protein coding features, 64% were assigned putative functions. Over 95% of proteins with coding features were forward-transcribed genes, comprising Major capsid protein, Head-tail adaptor, major tail protein, tail assembly chaperone, tape measure protein, membrane protein, DNA methylase, DNA polymerase Serine Intergrase, Transport protein and Endolysin.