Biodegradation of low-molecular-weight halogenated hydrocarbons by methanotrophic bacteria

Abstract Low-molecular-weight halogenated hydrocarbons are susceptible to degradation by anaerobic and aerobic bacteria. The methanotrophic bacterium Methylosinus trichosporium 0B3b degrades trichloroethylene more rapidly than other bacteria examined to date. Expression of soluble methane monooxygenase (MMO) is correlated with high rates of biodegradation.
An analysis of 16 S rRNA sequences of 11 ribosomal RNAs from type I, type II and type X methanotrophs and methanol-utilizing bacteria have revealed four clusters of phytogenetically related methylotrophs. This information may be useful for the identification and enumeration of methylotrophs in bioreactors and other environments during remediation of contaminated waters.     

Activation of store-operated Ca2+ current in Xenopus oocytes requires SNAP-25 but not a diffusible messenger.

Depletion of Ca2+ stores in Xenopus oocytes activated entry of Ca2+ across the plasma membrane, which was measured as a current I(soc) in subsequently formed cell-attached patches. I(soc) survived excision into inside-out configuration. If cell-attached patches were formed before store depletion, I(soc) was activated outside but not inside the patches. I(soc) was potentiated by microinjection of Clostridium C3 transferase, which inhibits Rho GTPase, whereas I(soc) was inhibited by expression of wild-type or constitutively active Rho. Activation of I(soc) was also inhibited by botulinum neurotoxin A and dominant-negative mutants of SNAP-25 but was unaffected by brefeldin A. These results suggest that oocyte I(soc) is dependent not on aqueous diffusible messengers but on SNAP-25, probably via exocytosis of membrane channels or regulatory molecules.     

Activity and Compartmentation of Photosynthetic Carboxylases in Normal and Chloroplast-mutant Maize Leaves

The activity of ribulose-l,5-diphosphate carboxylase (RudiP-carboxylase) and phosphoenolpyruvate carboxylase (PEP-carboxylase) measured in vitro was independent from the chlorophyll content of the leaves. The relatively high activity of PEP-carboxylase as compared to the RudiP-carboxylase activity was particularly pronounced in the mutants. Realization of the potential (in vitro measured) carboxylating activities in fixation of CO₂in vivo was practically complete in normal leaves. In the mutants, however, CO₂ fixation was lower than the level permitted by the carboxylase activity. This could be explained only in part by the impaired rate of photophosphorylation. Compartmentation of PEP-carboxylase was different in normal and mutant leaves: in contrast to the normal ones, parenchyma-sheath cells of the mutants exhibited high PEP-carboxylase activity. Competition of PEP-carboxylase with RudiP-carboxylase for CO₂ in the mutants led to accumulation of organic acids, and can account for their low photosynthetic activity.     

Phenotypic and functional analysis of gamma delta T cell receptor-positive murine dendritic epidermal clones

Thy-1+ dendritic cells isolated from the epidermis of normal mice (dEC)3 bear the gamma delta TCR associated with the CD3 complex. We have analyzed the effects of antibodies directed against the TCR complex, Ly-6C, and Thy-1, as well as pharmacologic agents which have been shown to activate T cells without engagement of the TCR complex, on levels of intracellular free calcium, activation of protein kinase C, cytolysis, IL-2R expression, and secretion of lymphokines by dEC clones. We have found that the dEC cells express a fully functional TCR complex which can function to transmit signals upon perturbation leading to an increase in IL-2R expression, release of lymphokines, and cytolytic activity. These results indicate that the gamma delta TCR+ dEC are capable of responding to activation signals in the same manner as mature alpha beta TCR+ cells and suggests that they may play a functional role in the skin.