Abstract

Most bacterial cells in nature exhibit extremely low colony-forming activity, despite showing various signs of viability, impeding the isolation and utilization of many bacterial resources. However, the general causes responsible for this state of low colony formation are largely unknown. Because liquid cultivation typically yields more bacterial cell cultures than traditional solid cultivation, we hypothesized that colony formation requires one or more specific gene functions that are dispensable or less important for growth in liquid media. To verify our hypothesis and reveal the genetic background limiting colony formation among bacteria in nature, we isolated Escherichia coli mutants that had decreased frequencies of colony formation but could grow in liquid medium from a temperature-sensitive mutant collection. Mutations were identified in fabB, which is essential for the synthesis of long unsaturated fatty acids. We then constructed a fabB deletion mutant in a wild-type background. Detailed behavioural analysis of the mutant revealed that under fatty acid-limited conditions, colony formation on solid media was more sensitively and seriously impaired than growth in liquid media. Furthermore, growth under partial inhibition of fatty acid synthesis with cerulenin or triclosan brought about similar phenotypes, not only in E. coli but also in Bacillus subtilis and Corynebacterium glutamicum. These results indicate that fatty acids have a critical importance in colony formation and that depletion of fatty acids in the environment partly accounts for the low frequency of bacterial colony formation.

Highlights

  • Micro-organisms, those in the domain Bacteria, are the dominant cellular life forms on Earth, with enormous diversity in genes and bioactive metabolites

  • We screened for mutants that could grow in liquid medium at non-permissive temperatures

  • We aimed to reveal the genetic background limiting bacterial colony formation, and in particular that causing growth differences between solid and liquid culture

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Summary

Introduction

Micro-organisms, those in the domain Bacteria, are the dominant cellular life forms on Earth, with enormous diversity in genes and bioactive metabolites. Numerous studies have reported that only a tiny fraction of bacterial cells living in nature can form colonies on agar plates [1, 2]. This low frequency of colony formation imposes severe limitations on our knowledge and utilization of enormous bacterial resources for biotechnological and medical applications. Recent advances in microdevices, combined with previous knowledge, have enabled high-throughput culturing techniques to be developed [20,21,22,23,24]. There is no persuasive general explanation regarding what makes bacteria in nature so difficult to culture on solid media

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