Bacterial adenine cross-feeding stems from a purine salvage bottleneck

Author:

Chuang Ying-Chih12,Haas Nicholas W1,Pepin Robert3,Behringer Megan G4,Oda Yasuhiro5,LaSarre Breah16,Harwood Caroline S5,McKinlay James B1

Affiliation:

1. Department of Biology, Indiana University , Bloomington, IN 47405 , United States

2. Biochemistry Program, Indiana University , Bloomington, IN 47405 , United States

3. Department of Chemistry, Indiana University , Bloomington, IN 47405 , United States

4. Department of Biological Sciences, Vanderbilt University , Nashville, TN 37235 , United States

5. Department of Microbiology, University of Washington , Seattle, WA 98195 , United States

6. Department of Plant Pathology, Entomology, and Microbiology, Iowa State University , Ames, IA 50011 , United States

Abstract

Abstract Diverse ecosystems host microbial relationships that are stabilized by nutrient cross-feeding. Cross-feeding can involve metabolites that should hold value for the producer. Externalization of such communally valuable metabolites is often unexpected and difficult to predict. Previously, we discovered purine externalization by Rhodopseudomonas palustris by its ability to rescue an Escherichia coli purine auxotroph. Here we found that an E. coli purine auxotroph can stably coexist with R. palustris due to purine cross-feeding. We identified the cross-fed purine as adenine. Adenine was externalized by R. palustris under diverse growth conditions. Computational modeling suggested that adenine externalization occurs via diffusion across the cytoplasmic membrane. RNAseq analysis led us to hypothesize that adenine accumulation and externalization stem from a salvage pathway bottleneck at the enzyme encoded by apt. Ectopic expression of apt eliminated adenine externalization, supporting our hypothesis. A comparison of 49 R. palustris strains suggested that purine externalization is relatively common, with 16 strains exhibiting the trait. Purine externalization was correlated with the genomic orientation of apt, but apt orientation alone could not always explain purine externalization. Our results provide a mechanistic understanding of how a communally valuable metabolite can participate in cross-feeding. Our findings also highlight the challenge in identifying genetic signatures for metabolite externalization.

Funder

US Army Research Office

National Science Foundation

National Institutes of Health

Lilly Endowment, Inc.

IU Pervasive Technology Institute

Publisher

Oxford University Press (OUP)

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