, 2007). Although degradation of phenolic compounds has not been studied in detail in PM1, exposure of this strain to MTBE induces additional pathways for the degradation of aromatics such as benzene, toluene, and xylene. In a recent study employing PCR-denaturing gradient gel electrophoresis (DGGE) analysis of reverse-transcribed rRNA, active M. petroleiphilum was shown to accumulate in soils contaminated with penta-chlorophenol

(Cáliz et al., 2011). The specific Variovorax group (cluster C) was also represented by two sequences obtained from the midterm stage (sequences MID06_F3 and MID06_G7, OTU 7). Nevertheless, these two sequences were < 85% similar to Variovorax sp. HAB30. The ecological relevance of Variovorax sp. Rucaparib ic50 relies in the presence of a characteristic LmPH type, corresponding to highly active phenol-degrading enzymes with high semi-saturation constants according to determinations of kinetic Akt inhibitor parameters using isolated cultures (Futamata et al., 2005). Cluster D grouped sequences belonging to Gammaproteobacteria with a high-Ks LmPH, including Pseudomonas putida relatives. A single sequence from the initial stage (sequence INI06_A3, OTU 1)

was found in cluster D. Interestingly, this sequence contained the typical signature of low-Ks phenol hydroxylases at amino acid positions 252 and 253, and position in the high-Ks group should be confirmed by incubation experiments with isolated cultures. The number of bacterial OTUs remained at relatively low values (from 5 to 10) in the three samples analyzed. The bacterial community at the initial and midterm stages of decomposition showed a greater richness, greater diversity (Shannon’s H′), and greater evenness (E) of LmPH gene compared to the late

stage (Table 1). The significant decrease in richness and diversity values suggests a major specificity of phenol-degrading bacteria in the late-stage community. The results from the phenol-degrading bacterial community analysis showed a highest degree of specialization at the late decomposition stage. All LmPH genes obtained at the late stage, except for one, grouped in clusters A and E together with PAK5 sequences belonging to known high-affinity phenol degraders (Watanabe et al., 1996). On the contrary, at the initial stage, the lower bacterial biomass and weaker phenol oxidase activity may indicate that decomposition of the large recalcitrant plant molecules had not yet begun (Fig. 1, Artigas et al., 2011). At this first stage, bacterial communities are supposed to be defined by environmental conditions of the stream and random colonization of the leaf surface (Harrop et al., 2009; Marks et al., 2009). Differences in the community composition of potential phenol-degrading bacteria were tested from the tree topology using UniFrac and parsimony tests.