Conservation of 2° structure by complex rearrangement of base pairing and substitutions in 16S rRNA genes of S. woodyi (a and a′ and b and b′), C. cellulolyticum (c and c′ and d and d′), and P. profundum (e and e′ and f and f′). Each molecule was folded using a program based on thermodynamics (a, b, c, d, e, and f), as well as a program based on multiple sequence alignment (a′, b′, c′, d′, e′, and f′), as described in Materials and Methods. For thermodynamic folding, the regions 50 bp upstream of the first mutation and 50 bp downstream of the last mutation were used to create the structures for each rRNA molecule, while only the area of interest is shown. Nucleotides related to substitutions are highlighted in red and indels in green. For folding using the multiple-sequence-alignment approach, nucleotides making up noncanonical base pairs are highlighted in brown (35, 36). Segments of rrn16S of S. woodyi correspond to positions 965 through 1065 of rrnC16S and rrnD16S. The segments of rrnC16S (a and a′) and rrnD16S (b and b′) differ by 13 positions, all substitutions. Segments of rrn16S of C. cellulolyticum correspond to positions 31 through 256 of rrnA16S and rrnE16S. The segments of rrnA16S (c and c′) and rrnE16S (d and d′) differ by 28 positions, including 10 indels and 18 substitutions. Segments of rrn16S of P. profundum correspond to positions 129 through 254 of rrnC16S and rrnE16S. The segments of rrnC16S (e and e′) and rrnE16S (f and f′) differ by 12 positions, including 1 indel and 11 substitutions.