Title of article
MiaA (Rv2727c) mediated tRNA isopentenylation of Mycobacterium tuberculosis H37Rv
Author/Authors
Soman, Smitha School of Biotechnology - Gautam Buddha University, Gautam Budh Nagar, Greater Noida, Uttar Pradesh, India , Ram, Siya School of Biotechnology - Gautam Buddha University, Gautam Budh Nagar, Greater Noida, Uttar Pradesh, India
Pages
8
From page
97
To page
104
Abstract
tRNA modifications play a significant role in the structural stability as well as translational
fidelity in all organisms from bacteria to humans. They also play a major role in bacterial
physiology by regulating translation in response to various environmental stresses.
Modifications coming at the anticodon-stem loop (ASL) are particularly important as they
stabilize codon-anticodon interactions, ensuring accuracy and speed in decoding mRNAs
Addition of isopentenyl group (i6A) at A37 position by tRNA isopentenyltransferase (MiaA) is
a well conserved modification from bacteria to human. We studied M. tuberculosis MiaA from
strain H37Rv and identified the target tRNAs for this modification based on the A36A37A38
motif. i6A modification of target tRNAs tRNALeuCAA, tRNAPheGAA, tRNATrpCCA and
tRNASerCGA were further confirmed by isopentenyltransferase assay providing the substrate
DMAPP and recombinant MiaA enzyme.
Keywords
Tuberculosis , M. smegmatis , MiaA, i6A , DMAPP , Isopentenyl transferase
Journal title
Molecular Biology Research Communications
Serial Year
2022
Record number
2732511
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