The encoded enzyme may exhibit an unusual substrate preference in strain E1, because bacterial CYP153s are believed to act only on n-C5–n-C16 alkanes (van Beilen & Funhoff, 2007), while the other alkane-oxidizing system of isolate E1 enables the slow degradation of the n-C20 alkane substrate http://www.selleckchem.com/products/apo866-fk866.html in the alkB-rub-deficient strain. The disruption mutant described in this study

serves as the basis of further investigations relating to the analysis of other n-alkane-degrading enzymes such as CYP153s in Dietzia spp. Furthermore, the presented genetic tools can support the future research of other Dietzia strains at the molecular level. This work was supported by the NKTH grant GVOP-3.1.1.-2004-05-0133/3.0, by the János Bolyai Research Scholarship of the Hungarian Academy of Sciences, and by the Bay Zoltán Foundation for Applied Research. Table S1. QPCR oligonucleotide primers used in this study. Please note: Wiley-Blackwell is not responsible for the content or functionality of any supporting materials supplied by the authors. Any queries (other than missing material)

should be directed to the corresponding author for the article. “
“Staphylococcus selleck inhibitor aureus possesses two distinct cardiolipin (CL) synthase genes, cls1 and cls2. It was previously shown that cls2 encodes a housekeeping-type CL synthase. However, the role of cls1 is elusive; a cls1 mutant was found to be equal to the wild type in terms of CL accumulation and stress tolerance. Here, we report that the physiological role of cls1 is to synthesize

CL under conditions of acute low-pH stress. Below pH 2.6, the cls1 mutant (i.e. carrying Cls2 alone) could not produce CL, while the cls2 mutant (carrying Cls1) effectively accumulated CL. The cls1-dependent CL production was quick (within 5 min) and did not require de novo protein ioxilan synthesis. Together with the results of phylogenetic analyses, our findings suggest that cls1 was generated through the duplication of cls2 after the divergence of the genus Staphylococcus and that the alternative CL synthase encoded by this gene confers improved survival in the face of acute acid stress. Staphylococcus aureus is a Gram-positive bacterium that naturally inhabits the nasal cavity of warm-blooded animals. It has a number of characteristics that allow it to survive host bactericidal responses and stressors associated with the surface environment, including drastic changes in osmotic pressure (Clements & Foster, 1999; Garzoni & Kelley, 2009; Morikawa et al., 2010). It is also an opportunistic pathogen that causes a wide range of diseases in both immunologically normal and compromised hosts. Importantly, methicillin-resistant strains (MRSA) are now the most common cause of nosocomial S. aureus infections and are spreading throughout communities (Chambers & Deleo, 2009).