Rhizopine biosensors for plant‐dependent control of bacterial gene expression

Author:

Haskett Timothy L.1ORCID,Geddes Barney A.12ORCID,Paramasivan Ponraj3ORCID,Green Patrick1,Chitnavis Samir1,Mendes Marta D.1,Jorrín Beatriz1ORCID,Knights Hayley E.1ORCID,Bastholm Tahlia R.4ORCID,Ramsay Joshua P.4ORCID,Oldroyd Giles E. D.35ORCID,Poole Philip S.1ORCID

Affiliation:

1. Department of Plant Sciences University of Oxford Oxford UK

2. Department of Microbiological Sciences North Dakota State University Fargo North Dakota USA

3. Sainsbury Laboratory University of Cambridge Cambridge UK

4. Curtin Medical School and Curtin Health Innovation Research Institute Curtin University Perth Western Australia Australia

5. Crop Science Centre University of Cambridge Cambridge UK

Abstract

AbstractEngineering signalling between plants and microbes could be exploited to establish host‐specificity between plant‐growth‐promoting bacteria and target crops in the environment. We previously engineered rhizopine‐signalling circuitry facilitating exclusive signalling between rhizopine‐producing (RhiP) plants and model bacterial strains. Here, we conduct an in‐depth analysis of rhizopine‐inducible expression in bacteria. We characterize two rhizopine‐inducible promoters and explore the bacterial host‐range of rhizopine biosensor plasmids. By tuning the expression of rhizopine uptake genes, we also construct a new biosensor plasmid pSIR05 that has minimal impact on host cell growth in vitro and exhibits markedly improved stability of expression in situ on RhiP barley roots compared to the previously described biosensor plasmid pSIR02. We demonstrate that a sub‐population of Azorhizobium caulinodans cells carrying pSIR05 can sense rhizopine and activate gene expression when colonizing RhiP barley roots. However, these bacteria were mildly defective for colonization of RhiP barley roots compared to the wild‐type parent strain. This work provides advancement towards establishing more robust plant‐dependent control of bacterial gene expression and highlights the key challenges remaining to achieve this goal.

Funder

Australian Research Council

Biotechnology and Biological Sciences Research Council

Gatsby Charitable Foundation

National Science Foundation

Royal Commission for the Exhibition of 1851

Publisher

Wiley

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