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Journal of Bacteriology, September 2001, p. 4958-4963, Vol. 183, No. 17
National Food Research Institute, Tsukuba,
Ibaraki 305-8642, Japan
Received 12 April 2001/Accepted 7 June 2001
To investigate the function of ribosomal proteins and translational
factors in Bacillus subtilis, we developed an in vivo assay system to measure the level of nonsense readthrough by utilizing the LacZ-LacI system. Using the in vivo nonsense readthrough assay system which we developed, together with an in vitro poly(U)-directed cell-free translation assay system, we compared the processibility and
translational accuracy of mutant ribosomes with those of the wild-type
ribosome. Like Escherichia coli mutants, most S12
mutants exhibited lower frequencies of both UGA readthrough and
missense error; the only exception was a mutant (in which Lys-56 was
changed to Arg) which exhibited a threefold-higher frequency of
readthrough than the wild-type strain. We also isolated several
ribosomal ambiguity (ram) mutants from an S12 mutant.
These ram mutants and the S12 mutant mentioned above (in
which Lys-56 was changed to Arg) exhibited higher UGA readthrough
levels. Thus, the mutation which altered Lys-56 to Arg resulted in a
ram phenotype in B. subtilis. The
efficacy of our in vivo nonsense readthrough assay system was
demonstrated in our investigation of the function of ribosomal proteins
and translational factors.
0021-9193/01/$04.00+0 DOI: 10.1128/JB.183.17.4958-4963.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Construction of an In Vivo Nonsense Readthrough
Assay System and Functional Analysis of Ribosomal Proteins S12, S4,
and S5 in Bacillus subtilis
*
Corresponding author. Mailing address: National Food
Research Institute, 2-1-12 Kannondai, Tsukuba, Ibaraki 305-8642, Japan. Phone: 81-298-38-8125. Fax: 81-298-38-7996. E-mail:
kochi{at}affrc.go.jp.
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