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RB-TnSeq data for Bacteroides thetaiotaomicron VPI-5482

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posted on 2020-10-30, 21:01 authored by Hualan Liu, veronica escalante, Peter Turnbaugh, Hans Carlson, Morgan PriceMorgan Price, Adam DeutschbauerAdam Deutschbauer
This data set includes 523 successful fitness assays for Bacteroides thetaiotaomicron VPI-5482 based on a pool of randomly-barcoded transposon mutants (RB-TnSeq). The data is provided as a gzipped tarball. After unpacking, load index.html into a web browser to get some explanation of all the files.

Note added September 10, 2021: After publishing this data, Morgan Price and Adam Deutschbauer discovered that our stock solutions for sucrose and D-mannitol were problematic. In particular, Escherichia coli BW25113 is a K-12 strain (closely related to MG1655) and should not be able to grow on sucrose. In M9 media made with our original stock solution of sucrose, E. coli BW25113 grew, but in media made with a fresh stock solution, it did not. Similarly, growth of E. coli on mannitol should require the phosphotransferase uptake protein mtlA and the dehydrogenase mtlD. In our original fitness assays for E. coli, mtlA and mtlD were not important for growth on mannitol; instead, manX and manY, which encode the mannose phosphotransferase system, were important. When we repeated these experiments with a fresh stock solution for D-mannitol, we found that mtlA and mtlD were important for fitness, and manX and manY were not.

Please disregard the data regarding sucrose or D-mannitol. In the Fitness Browser (https://fit.genomics.lbl.gov), the problematic fitness experiments have been removed. As of September 2021, the data for these compounds in the Fitness Browser is from fresh stock solutions of sucrose and D-mannitol. We also checked that the data from these experiments is consistent with prior knowledge of the utilization of these compounds. Finally, we checked the gene re-annotations that were related to these sucrose or mannitol utilization.

Funding

DOE DE-AC02-05CH11231

National Institutes of Health R01 HL122593

Damon Runyon Cancer Research Foundation grant DRR-42-16

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