Search bioRxiv⌕ Search

Biology subjects

Bruckbauer, S. T.

Publications and source records attributed to Bruckbauer, S. T..

2 recordsLinked to original sources

Experimental evolution of extremophile levels of radiation resistance in Escherichia coli

Recent human development of high-level sources of ionizing radiation (IR) prompts a corresponding need to understand the effects of IR on living systems. One approach has focused on the capacity of some organisms to survive astonishing levels of IR exposure. Using experimental evolution, we have generated populations of Escherichia coli with IR resistance comparable to the extremophile Deinococcus radiodurans. Every aspect of cell physiology is affected. Cellular isolates exhibit approximately 1,000 base pair changes plus major genomic and proteomic alterations. The IR resistance phenotype is stable without selection for at least 100 generations. Defined and probable contributions include alterations in cellular systems involved in DNA repair, amelioration of reactive oxygen species, Fe metabolism and repair of iron-sulfur centers, DNA packaging, and intermediary metabolism. A path to new mechanistic discoveries, exemplified by an exploration of rssB function, is evident. Most important, there is no single molecular mechanism underlying extreme IR resistance.

evolutionary biology↗

A hyperactive variant of the Escherichia coli anaerobic transcription factor FNR enhances ionizing radiation resistance

We have previously generated four replicate populations of ionizing radiation (IR)- resistant Escherichia coli though directed evolution. Sequencing of isolates from these populations revealed that mutations affecting DNA repair (through DNA double-strand break repair and replication restart), ROS amelioration, and cell wall metabolism were prominent. Three mutations involved in DNA repair explained the IR resistance phenotype in one population, and similar DNA repair mutations were prominent in two others. The remaining population, IR-3-20, had no mutations in the key DNA repair proteins, suggesting that it had taken a different evolutionary path to IR resistance. Here, we present evidence that a variant of the anaerobic metabolism transcription factor FNR isolated from population IR-3-20 can play a role in IR resistance. An FNR variant is unique to IR-3-20 and suggests a role for altered global metabolism through the FNR regulon as a means for experimentally-evolved IR resistance.

evolutionary biology↗