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 Phosphate starvation response controls genes required to synthesize the phosphate analog arsenate

Qian Wang, Yoon-Suk Kang, Abdullah Alowaifeer, Kaixiang Shi, Xia Fan, Lu Wang, Jonathan Jetter, Brian Bothner, Gejiao Wang* and Timothy R. McDermott**

Environmental arsenic poisoning affects roughly 200 million people worldwide. The toxicity and mobility of
arsenic in the environment is significantly influenced by microbial redox reactions, with arsenite (AsIII)
being more toxic than arsenate (AsV). Microbial oxidation of AsIII to AsV is known to be regulated by the
AioXSR signal transduction system and viewed to function for detoxification or energy generation. Here, we show that AsIII oxidation is ultimately regulated by the phosphate starvation response (PSR), requiring the sensor kinase PhoR for expression of the AsIII oxidase structural genes aioBA. The PhoRB and AioSR signal transduction systems are capable of transphosphorylation cross-talk, closely integrating AsIII oxidation with the PSR. Further, under PSR conditions, AsV significantly extends bacterial growth and accumulates in the lipid fraction to the apparent exclusion of phosphorus. This could spare phosphorus for nucleic acid synthesis or triphosphate metabolism wherein unstable arsenic esters are not tolerated, thereby enhancing cell survival
potential. We conclude that AsIII oxidation is logically part of the bacterial PSR, enabling the synthesis of
the phosphate analog AsV to replace phosphorus in specific biomolecules or to synthesize other molecules
capable of a similar function, although not for total replacement of cellular phosphate.



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