RESUMO
Four subcluster L2 mycobacteriophages, Finemlucis, Miley16, Wilder, and Zakai, that infect Mycobacterium smegmatis mc2155 were isolated. The four phages are closely related to each other and code for 12 to 14 tRNAs and 130 to 132 putative protein-coding genes, including tyrosine integrases, cro, immunity repressors, and excise genes involved in the establishment of lysogeny.
RESUMO
Over multiple response opportunities, recall may be inconsistent. For example, an eyewitness may report information at trial that was not reported during initial questioning-a phenomenon called reminiscence. Such inconsistencies are often assumed by lawyers to be inaccurate and are sometimes interpreted as evidence of the general unreliability of the rememberer. In two experiments, we examined the output-bound accuracy of inconsistent memories and found that reminisced memories were indeed less accurate than memories that were reported consistently over multiple opportunities. However, reminisced memories were just as accurate as memories that were reported initially but not later, indicating that it is the inconsistency of recall, and not the later addition to the recall output, that predicts lower accuracy. Finally, rememberers who exhibited more inconsistent recall were less accurate overall, which, if confirmed by more ecologically valid studies, may indicate that the common legal assumption may be correct: Witnesses who provide inconsistent testimony provide generally less trustworthy information overall.
RESUMO
We investigated the Acinetobacter baylyi gene ACIAD1960, known from previous work to be expressed during long-term stationary phase. The protein encoded by this gene had been annotated as a Conserved Hypothetical Protein, surrounded by putative tellurite resistance ("Ter") proteins. Sequence analysis suggested that the protein belongs to the DUF1796 putative papain-like protease family. Here, we show that the purified protein, subsequently named StiP, has cysteine protease activity. Deletion of stiP causes hypersensitivity to tellurite, altered population dynamics during long-term batch culture, and most strikingly, dramatic alteration of normal cell morphology. StiP and associated Ter proteins (the StiP-Ter cluster) are therefore important for regulating cell morphology, likely in response to oxidative damage or depletion of intracellular thiol pools, triggered artificially by tellurite exposure. Our finding has broad significance because while tellurite is an extremely rare compound in nature, oxidative damage, the need to maintain a particular balance of intracellular thiols, and the need to regulate cell morphology are ubiquitous.