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. 2021 Jul 6;16(7):e0253267. doi: 10.1371/journal.pone.0253267

Table 2. Modification detection by SMRT sequencing.

(dam GATC m6A reported for E. coli clones expressing dam MTase)
Enzyme MTase construct am4C % detected Coverage dam m6A %
BspHIV CGCCC
Native organism 98.5 181x na
M.BspHIV-pRRS 97.6 90x 99.9
CinI GAACT
Native organism 98.4 146x na
M.CinI-pRRS 25.3 82x 99.9
DthLIII CACC
Native organism 85.5 550x na
M.DthLIII-pRRS 0 93x 99.9
M.DthLIII+R.DthLIII-pRRS 90.6 2954x 100
Eco86II GAGCC
Native organism 92.3 77x 99.6
M.Eco86II-pRRS 98.9 76x 99.9
FnoB1III CGCC
Native organism 47 not reported na
M.FnoB1III-pRRS 0 81x 99.9
M.FnoB1III+R.FnoB1III-pRRS 63.7 163x 99.9
PleII CACCGC
Native organism 99.9 158x na
M.PleII-pRRS 73.9 86x 99.9
M.PleII-pRRS CACCNC "star" 69.3 86x 99.9

a"m4C percent detected" is percent of m4C motifs called as modified using the standard PacBio methylome analysis with default settings. Coverage is per strand for the motif. dam m6A methylation calls are shown as a control for systems expressed in E. coli carrying the dam methyltransferase.