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. 2024 Sep 5;14:20664. doi: 10.1038/s41598-024-71248-y

Fig. 4.

Fig. 4

Stability and degradation of RecA splicing products. (A, B) Mid-log Mtb cultures were treated with Mitomycin C (MMC) for 24 h, then treated with chloramphenicol (CAM) for the indicated times to block new protein synthesis. (A) Western blot analysis of intein levels over time. Top: Representative blot. Bottom: Quantification of 3 biological repeats normalized to GFP. (B) Western blot analysis of ligated extein levels over time. Top: Representative blot. Bottom: Quantification of 3 biological repeats normalized to GFP. (C, D) Mtb cultures were treated ( +) with bortezomib (BTZ) to block proteasome activity or left untreated (−). (C) Western blot analysis of intein levels over time. Top: Representative blot. Bottom: Quantification of 3 biological repeats normalized to GFP. (D) Western blot analysis of ligated extein, LE, NEA, and NE levels after BTZ treatment. Top: Representative blot. Bottom: Quantification of 3 biological repeats normalized to GFP; ** indicates p < 0.01.