Bacterial adenine cross-feeding stems from a purine salvage bottleneck.

IF 10.8 1区 环境科学与生态学 Q1 ECOLOGY
Ying-Chih Chuang, Nicholas W Haas, Robert Pepin, Megan G Behringer, Yasuhiro Oda, Breah LaSarre, Caroline S Harwood, James B McKinlay
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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.

细菌腺嘌呤交叉进食源于嘌呤挽救瓶颈。
多样化的生态系统寄生着微生物关系,这种关系通过营养物质的交叉互哺而得以稳定。交叉互哺可能会产生对生产者有价值的代谢物。这种具有公共价值的代谢物的外化往往出人意料,而且难以预测。在此之前,我们发现了古朴红假单胞菌(Rhodopseudomonas palustris)的嘌呤外化作用,因为它能够拯救大肠杆菌的嘌呤辅助营养体。在这里,我们发现大肠杆菌的嘌呤辅助营养体可以通过嘌呤交叉摄食与喙假单胞菌稳定共存。我们确定交叉进食的嘌呤为腺嘌呤。在不同的生长条件下,腺嘌呤会被巴氏梭菌外化。计算模型表明,腺嘌呤的外化是通过细胞质膜的扩散进行的。通过 RNAseq 分析,我们推测腺嘌呤的积累和外化源于 apt 所编码酶的挽救途径瓶颈。apt的异位表达消除了腺嘌呤外化,支持了我们的假设。对 49 株 R. palustris 菌株的比较表明,嘌呤外化现象比较普遍,有 16 株表现出这一特征。嘌呤外化与 apt 的基因组定向相关,但仅靠 apt 的定向并不能解释嘌呤外化。我们的研究结果从机理上揭示了一种具有公共价值的代谢物是如何参与交叉进食的。我们的发现还凸显了确定代谢物外化遗传特征的挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ISME Journal
ISME Journal 环境科学-生态学
CiteScore
22.10
自引率
2.70%
发文量
171
审稿时长
2.6 months
期刊介绍: The ISME Journal covers the diverse and integrated areas of microbial ecology. We encourage contributions that represent major advances for the study of microbial ecosystems, communities, and interactions of microorganisms in the environment. Articles in The ISME Journal describe pioneering discoveries of wide appeal that enhance our understanding of functional and mechanistic relationships among microorganisms, their communities, and their habitats.
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