Abstract

Studies on the halotolerance of bacteria are attractive to the fermentation industry. However, a lack of sufficient genomic information has precluded an investigation of the halotolerance of Halomonas beimenensis. Here, we describe the molecular mechanisms of saline adaptation in H. beimenensis based on high-throughput omics and Tn5 transposon mutagenesis. The H. beimenensis genome is 4.05 Mbp and contains 3,807 genes, which were sequenced using short and long reads obtained via deep sequencing. Sixteen Tn5 mutants with a loss of halotolerance were identified. Orthologs of the mutated genes, such as nqrA, trkA, atpC, nadA, and gdhB, have significant biological functions in sodium efflux, potassium uptake, hydrogen ion transport for energy conversion, and compatible solute synthesis, which are known to control halotolerance. Other genes, such as spoT, prkA, mtnN, rsbV, lon, smpB, rfbC, rfbP, tatB, acrR1, and lacA, function in cellular signaling, quorum sensing, transcription/translation, and cell motility also shown critical functions for promoting a halotolerance. In addition, KCl application increased halotolerance and potassium-dependent cell motility in a high-salinity environment. Our results demonstrated that a combination of omics and mutagenesis could be used to facilitate the mechanistic exploitation of saline adaptation in H. beimenensis, which can be applied for biotechnological purposes.

Highlights

  • Lines WT rfbP rfbC lon smpB trkA2 gdhB mtnN2 tatB spoT prkA rsbV acrR1 atpC nqrA nadA lacA

  • We calculated the length of the lag phase of H. beimenensis under various NaCl conditions

  • These results indicated that the optimal growth condition for H. beimenensis is 5% NaCl

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Summary

Introduction

Lines WT rfbP rfbC lon smpB trkA2 gdhB mtnN2 tatB spoT prkA rsbV acrR1 atpC nqrA nadA lacA. Sodium ion efflux and hydrogen and potassium ion uptake help maintain bacterial osmotic balance in high-salinity environments. The operation of the respiratory chain generates an electrochemical sodium gradient to pump out sodium to maintain osmotic balance while NADH is oxidized by Na+-NQR9. Flagellum-related genes have been found to be down-regulated in highly saline environments, suggesting that decreased cell motility allows more energy to be available for osmoprotection[11,12]. Another explanation is that cell motility is correlated with sodium-driven motor activity[11]. Decreased motor activity can reduce sodium re-entry to maintain intracellular ion homeostasis[11]

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