Search

Even though compelling evidences indicate that marine microbes show biogeographic patterns, very little is known on the mechanisms driving those patterns in aquatic ecosystems. In the present study, bacterial community structure was examined in epipelagic waters of a highly hydrodynamic area of the Southern Ocean to gain insight into the role that biogeochemical factors and water mass mixing (a proxy of dispersal) have on microbial biogeography. Four water masses that converge and mix around the South Shetland Islands (northern tip of the Antarctic Peninsula) were investigated. Bacterioplankton communities were water-mass specific, and were best explained by dispersal rather than by biogeochemical factors, which is attributed to the relatively reduced environmental gradients found in these cold and nutrient rich waters. These results support the notion that currents and water mixing may have a considerable effect in connecting and transforming different water bodies, and consequently, in shaping communities of microorganisms. Considering the multidimensional and dynamic nature of the ocean, analysis of water mass mixing is a more suitable approach to investigate the role of dispersal on the biogeography of planktonic microorganisms rather than geographical distance., (© 2016 Society for Applied Microbiology and John Wiley & Sons Ltd.)

Polyhydroxyalkanoates (PHAs) are biodegradable polymers produced by a wide range of bacteria, including Pseudomonads. These polymers are accumulated in the cytoplasm as carbon and energy storage materials when culture conditions are unbalanced and hence, they have been classically considered to act as sinks for carbon and reducing equivalents when nutrients are limited. Bacteria facing carbon excess and nutrient limitation store the extra carbon as PHAs through the PHA polymerase (PhaC). Thereafter, under starvation conditions, PHA depolymerase (PhaZ) degrades PHA and releases R-hydroxyalkanoic acids, which can be used as carbon and energy sources. To study the influence of a deficient PHA metabolism in the growth of Pseudomonas putida KT2442 we have constructed two mutant strains defective in PHA polymerase (phaC1)- and PHA depolymerase (phaZ)-coding genes respectively. By using these mutants we have demonstrated that PHAs play a fundamental role in balancing the stored carbon/biomass/number of cells as function of carbon availability, suggesting that PHA metabolism allows P. putida to adapt the carbon flux of hydroxyacyl-CoAs to cellular demand. Furthermore, we have established that the coordination of PHA synthesis and mobilization pathways configures a functional PHA turnover cycle in P. putida KT2442. Finally, a new strain able to secrete enantiomerically pure R-hydroxyalkanoic acids to the culture medium during cell growth has been engineering by redirecting the PHA cycle to biopolymer hydrolysis.