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. 2006 Feb 10;7(4):411–417. doi: 10.1038/sj.embor.7400641

Table 1.

Complementation of the Escherichia coli RNase P mutant strain by Bacillus subtilis rnpB

 
DW2/pDW160
DW2 doubling time (min)*
RNase P RNA source 30°C 43°C 37°C
pSP64-EcrnpB
+++
+++
75±7
pSP64-BsrnpB
+++
+++§
64±4
pSP64 +++  
Growth of mutant strains transformed with E. coli or B. subtilis rnpB was analysed on LB plates at the permissive (30°C) and non-permissive (43°C) temperature. RNase P, ribonuclease P; +++, good complementation; —, no colonies.
*Measured after elimination of pDW160.
Colonies at 43°C were smaller than those at 30°C; for growth at 43°C, the phenotype of cells transformed with E. coli rnpB was set as the standard.
§Colonies at 43°C were larger than those for cells transformed with E. coli rnpB, set as the standard.