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The first step of biodegradation is the contact of microorganism and pollutants, in order to examine the influence of phenanthrene on Sphingomonas sp. GY2B's surface properties during its degrading process, the bacteria was cultivated at different conditions, and detected by flow cytometry combined with fluorescent dyes for its surface changes. The results indicated that, the membrane structure had been certainly damaged during the degrading process, leading to an increased membrane permeability. Moreover, the destruction of bacteria membrane integrity became more serious with a higher pollutant concentration. At the concentration of 300 mg x L(-1), the ratio of stained bacterial cells/unstained cells was 12.44 after cultured for 60 h, while at 100 mg x L(-1) and 1.2 mg x L(-1), the ratios were 1.95 and 1.11, respectively. The results of fourier transform infrared (FT-IR) absorbance spectroscopy detection, the discrimination of death, injured and intact cells, and Zeta potential detection further verified the bacterial cell surface permeability changes. Flow cytometry combined with fluorescent dye propidium iodide was used to monitor the changes of bacterial membrane integrity on single-cell level which exhibited a good potential for exploring the changes of bacterial surface properties during the degrading progress and more deeply for investigating the degradation mechanism.

The effect of the biosurfactant rhamnolipid on phenanthrene biodegradation and cell growth of phenanthrene degraders was investigated. To compare the effect of rhamnolipid addition, two bacterial strains, 3Y and 4-3, which were isolated from a diesel-contaminated site in Korea, were selected. Without the biosurfactant, large amounts of phenanthrene were degraded with both strains at neutral pH, with higher rates of phenanthrene degradation when the cell growth was higher. Upon the addition of 240 mg/L rhamnolipid, the phenanthrene degradation and optical density were reduced, with this inhibitory effect similar for both 3Y and 4-3. To explain this inhibition, the cell growths of both strains were monitored with various concentrations of rhamnolipid, which showed significant toxic effects toward strain 3Y, but was nontoxic toward 4-3. Combining the inhibitory and toxicity results with regard to the biodegradation, different mechanisms can be suggested for each strain. In the biodegradation experiments, the toxicity of rhamnolipid itself mainly was responsible for the inhibitory effect in the case of 3Y, whereas the toxicity of solubilized phenanthrene or the increased toxicity of rhamnolipid in the presence of solubilized phenanthrene could have resulted in the inhibitory effect in the case of 4-3. This study demonstrated that the effectiveness of biosurfactant-enhanced biodegradation can be significantly different depending on the strain, and the toxicity of the biosurfactant should be considered as an important factor.

An extension of the models developed by Guha and Jaffé (Biotechnol Bioeng [1996] 50:693-699) to describe the phenanthrene biodegradation kinetics for the cultures with variable fractional volumes is presented. Batch experiments were conducted with a culture capable of degrading the phenanthrene using a single culture vessel from which samples were withdrawn over time to monitor the disappearance of phenanthrene. For accurate measurement of phenanthrene concentrations, a sampling procedure designed for quantifying the sorption of phenanthrene onto glassware was also introduced. The Monod parameters were estimated by nonlinear regression analyses of simultaneous solutions to the substrate utilization/volatilization and Monod equations for growth of the cell mass. The results demonstrate that the models were able to be extended to phenanthrene-degrading cultures with variable fractional volumes. When the ratio between sampling volume and volume of the culture medium was relatively small, the parameters obtained were similar to those which would be obtained using constant fractional volumes of culture medium. It was also found that the model's fit to the phenanthrene disappearance data in this study were better than those obtained by Guha and Jaffé, implying that the sorption process of phenanthrene during the sampling period could significantly affect the measurement of phenanthrene concentrations. Failing to account for these losses led to less accurate measurements of substrate concentrations, which in turn resulted in a poor estimation of the parameters. The findings of this study reduce considerably the experimental work necessary in the estimation of Monod kinetic parameters for the purpose of modeling., (Copyright 2004 Wiley Periodicals, Inc.)