Abstract

Most studies investigating mechanisms that confer microorganisms with tolerance to solvents have often focused on adaptive responses following exposure, while less attention has been given to inherent, or constitutive, processes that prevail at the onset of exposure to a toxic solvent. In this study, we investigated several properties of the highly solvent-tolerant bacterium Rhodococcus sp. 33 that confer it with a tolerance to high concentrations of benzene. When challenged with liquid benzene, the growth of both nonadapted and adapted cells was decreased by 0.25¨C0.30% (v/v) liquid benzene, and higher concentrations (≤0.35% v/v) produced a complete cessation in the growth of only nonadapted cells. When exposed to presolubilized benzene, nonadapted cells tolerated ≥1000 mg/l, whereas adapted cells tolerated >1400 mg/l. Measuring the cell membrane fluidity of the cells during these exposure experiments showed that at the onset of exposure, the membranes of adapted cells were less affected by benzene compared to nonadapted cells, although these effects were insignificant in the long term. Several benzene-sensitive mutants were generated from this Rhodococcus, two of which were unable to degrade benzene, yet they still tolerated 500¨C800 mg/l. This confirmed our earlier work suggesting that the benzene-degradation pathway of this organism plays a minor role in tolerance. Under the phase and transmission electron microscope, the mutants were found to have lost the ability to produce extracellular polymers, and many cells appeared pleomorphic, containing intracellular membrane invaginations and mesosome-like structures. As will be discussed, these results identify important functions of the cell membrane, the cell wall, and extracellular polymer in their native state (i.e., before exposure) in conferring this organism with tolerance to benzene.

Highlights

  • Numerous advances have been made in recent years in our efforts to enhance the bioremediation of pollutants at contaminated sites

  • The organism used in this study was Rhodococcus sp. 33, a bacterium that was previously isolated from a contaminated site in Sydney, Australia, for its ability to degrade benzene[13]

  • From the remaining population of cells, i.e., the nongrowing benzene-sensitive population, a total of 48 colonies were isolated as benzene sensitive, based on their small colony size of ≤0.5 mm

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Summary

Introduction

Numerous advances have been made in recent years in our efforts to enhance the bioremediation of pollutants at contaminated sites. An important problem still encountered is the inherent toxicity of some pollutants to the microorganisms responsible for their degradation. This is especially true of aromatic hydrocarbons, such as benzene, toluene, and the xylene isomers (BTX). These compounds can cause total inhibition of microbial activity or lysis of cells[1]. In order for degradation to occur, the microorganisms must tolerate exposure to these compounds. Much research has been devoted to understanding the interactions between organic solvents and microbial cells, with a view to improving the tolerance and degradative ability of microorganisms[2]

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