Abstract
The tetranucleotide TpPsipCpGp, when bound to Escherichia coli 50S ribosomal subunits, can replace intact tRNA in the stringent factor-directed synthesis of guanosine tetra- and pentaphosphates. The TpPsipCpGp-dependent fragment reaction has a strict requirement for the 50S and 30S ribosomal subunits and synthetic or natural messenger RNA.
MeSH Terms
Bacterial Proteins/biosynthesis
Binding Sites
Chromatography, Gel
Depression, Chemical
Escherichia coli/metabolism
Guanine Nucleotides/biosynthesis
Oligonucleotides/metabolism
Protein Binding
Puromycin/pharmacology
RNA, Bacterial/biosynthesis,metabolism
RNA, Messenger/metabolism
RNA, Ribosomal/metabolism
RNA, Transfer/metabolism
Ribosomes/metabolism
Chemicals
Bacterial Proteins
Guanine Nucleotides
Oligonucleotides
RNA, Bacterial
RNA, Messenger
RNA, Ribosomal
Puromycin
RNA, Transfer
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Richter D
Erdmann V A
Sprinzl M
References (13)
13 references, click to expand
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