Evidence for an active dimer of Escherichia coli beta-galactosidase.

BETA-Galactosidase (EC 3.2.1.23), prepared from strains ML 308 and K12 3300 of Escherichia coli, dissociated into an inactive monomer in the presence of Ag+. When such a monomer preparation is treated with excess of thiol an enzymically active dimer is formed in addition to an active tetramer. It is suggested that Ag+ may be of value in studies on other multimeric proteins as a mild dissociating agent.     

Non-A, non-B hepatitis-related hepatocellular carcinoma in a chimpanzee

Epidemiology has indicated the possible association of non-A, non-B hepatitis (NANBH) with hepatocellular carcinoma (HCC) in man, but there are no means for confirmation. Chimpanzees are recognized models for studying hepatitis B and NANBH, and may become carriers of both. The first case of HCC to be reported in chimpanzees was found after longitudinal study of a hepatitis B-free chimpanzee 7 years after inoculation with human plasma from a patient reported to have chronic NANBH.     

Mycoplasma CG- and GATC-specific DNA methyltransferases selectively and efficiently methylate the host genome and alter the epigenetic landscape in human cells

Aberrant DNA methylation is frequently observed in disease, including many cancer types, yet the underlying mechanisms remain unclear. Because germline and somatic mutations in the genes that are responsible for DNA methylation are infrequent in malignancies, additional mechanisms must be considered. Mycoplasmas spp., including Mycoplasma hyorhinis, efficiently colonize human cells and may serve as a vehicle for delivery of enzymatically active microbial proteins into the intracellular milieu. Here, we performed, for the first time, genome-wide and individual gene mapping of methylation marks generated by the M. hyorhinis CG- and GATC-specific DNA cytosine methyltransferases (MTases) in human cells. Our results demonstrated that, upon expression in human cells, MTases readily translocated to the cell nucleus. In the nucleus, MTases selectively and efficiently methylated the host genome at the DNA sequence sites free from pre-existing endogenous methylation, including those in a variety of cancer-associated genes. We also established that mycoplasma is widespread in colorectal cancers, suggesting that either the infection contributed to malignancy onset or, alternatively, that tumors provide a favorable environment for mycoplasma growth. In the human genome, ∼11% of GATC sites overlap with CGs (e.g., CGAT^mCG); therefore, the methylated status of these sites can be perpetuated by human DNMT1. Based on these results, we now suggest that the GATC-specific methylation represents a novel type of infection-specific epigenetic mark that originates in human cells with a previous exposure to infection. Overall, our findings unveil an entirely new panorama of interactions between the human microbiome and epigenome with a potential impact in disease etiology.     

Deciphering Mode of Action of Heparanase Using Structurally Defined Oligosaccharides

Heparan sulfate (HS) is a highly sulfated polysaccharide that serves many biological functions, including regulating cell growth and inflammatory responses as well as the blood coagulation process. Heparanase is an enzyme that cleaves HS and is known to display a variety of pathophysiological effects in cancer, diabetes, and Alzheimer disease. The link between heparanase and diseases is a result of its selective cleavage of HS, which releases smaller HS fragments to enhance cell proliferation, migration, and invasion. Despite its importance in pathological diseases, the structural cues in HS that direct heparanase cleavage and the steps of HS depolymerization remain unknown. Here, we sought to probe the substrate specificity of heparanase using a series of structurally defined oligosaccharide substrates. The sites of heparanase cleavage on the oligosaccharide substrates were determined by mass spectrometry and gel permeation chromatography. We discovered that heparanase cleaves the linkage of glucuronic acid linked to glucosamine carrying 6-O-sulfo groups. Furthermore, our findings suggest that heparanase displays different cleavage modes by recognizing the structures of the nonreducing ends of the substrates. Our results deepen the understanding of the action mode of heparanase.     

Effects of crop field characteristics on nocturnal winter use by American woodcock

Since the late 1960s, American woodcock (Scolopax minor) have undergone population declines because of habitat loss. Previous research suggested ridge and furrow topography in conventionally tilled soybean fields provided critical nocturnal cover as birds foraged on earthworms. However, the use of no-till technology has increased and many fields now lack ridge and furrow topography. We assessed woodcock winter nocturnal foraging habitat use given recent changes in agricultural technology, and investigated how field treatment, earthworm abundance, and environmental variables affect the selection of nocturnal foraging sites. We counted woodcock along transects in 5 field treatments twice in each of 67 fields during December–March 2008–2009 and 72 fields during December–March 2009–2010. During both seasons, we collected earthworm and soil samples from a subset of fields of each field treatment. Woodcock densities were at least twice as high in no-till soybean fields planted after corn and in undisked corn fields with mowed stalks than in other field treatments. No-till soybean planted after corn and undisked corn fields contained ridge and furrow topography, whereas other crops did not, and earthworms were at least 1.5 times more abundant in no-till soybean fields than other field treatments. Ridges and furrows in no-till soybean fields planted after corn and undisked corn fields may provide wintering woodcock with thermal protection and concealment from predators. No-till soybean fields planted after corn offered the additional benefit of relatively high food availability. The presence of ridge and furrow topography can be used to predict woodcock field use on the wintering grounds in agricultural areas. Farmers can provide nocturnal winter foraging sites for woodcock by delaying field disking and leaving ridge and furrow topography in crop fields. © 2011 The Wildlife Society.     

The auxiliary protein complex SaePQ activates the phosphatase activity of sensor kinase SaeS in the SaeRS two‐component system of Staphylococcus aureus

In bacterial two‐component regulatory systems (TCSs), dephosphorylation of phosphorylated response regulators is essential for resetting the activated systems to the pre‐activation state. However, in the SaeRS TCS, a major virulence TCS of Staphylococcus aureus, the mechanism for dephosphorylation of the response regulator SaeR has not been identified. Here we report that two auxiliary proteins from the sae operon, SaeP and SaeQ, form a protein complex with the sensor kinase SaeS and activate the sensor kinase's phosphatase activity. Efficient activation of the phosphatase activity required the presence of both SaeP and SaeQ. When SaeP and SaeQ were ectopically expressed, the expression of coagulase, a sae target with low affinity for phosphorylated SaeR, was greatly reduced, while the expression of alpha‐haemolysin, a sae target with high affinity for phosphorylated SaeR, was not, demonstrating a differential effect of SaePQ on sae target gene expression. When expression of SaePQ was abolished, most sae target genes were induced at an elevated level. Since the expression of SaeP and SaeQ is induced by the SaeRS TCS, these results suggest that the SaeRS TCS returns to the pre‐activation state by a negative feedback mechanism.     

Discovery and optimization of potent and selective imidazopyridine and imidazopyridazine mTOR inhibitors

mTOR is a critical regulator of cellular signaling downstream of multiple growth factors. The mTOR/PI3K/AKT pathway is frequently mutated in human cancers and is thus an important oncology target. Herein we report the evolution of our program to discover ATP-competitive mTOR inhibitors that demonstrate improved pharmacokinetic properties and selectivity compared to our previous leads. Through targeted SAR and structure-guided design, new imidazopyridine and imidazopyridazine scaffolds were identified that demonstrated superior inhibition of mTOR in cellular assays, selectivity over the closely related PIKK family and improved in vivo clearance over our previously reported benzimidazole series.     

An unusual signal peptide extension inhibits the binding of bacterial presecretory proteins to the signal recognition particle, trigger factor, and the SecYEG complex

Considerable evidence indicates that the Escherichia coli signal recognition particle (SRP) selectively targets proteins that contain highly hydrophobic signal peptides to the SecYEG complex cotranslationally. Presecretory proteins that contain only moderately hydrophobic signal peptides typically interact with trigger factor (TF) and are targeted post-translationally. Here we describe a striking exception to this rule that has emerged from the analysis of an unusual 55-amino acid signal peptide associated with the E. coli autotransporter EspP. The EspP signal peptide consists of a C-terminal domain that resembles a classical signal peptide plus an N-terminal extension that is conserved in other autotransporter signal peptides. Although a previous study showed that proteins containing the C-terminal domain of the EspP signal peptide are targeted cotranslationally by SRP, we found that proteins containing the full-length signal peptide were targeted post-translationally via a novel TF-independent mechanism. Mutation of an invariant asparagine residue in the N-terminal extension, however, restored cotranslational targeting. Remarkably, proteins containing extremely hydrophobic derivatives of the EspP signal peptide were also targeted post-translationally. These and other results suggest that the N-terminal extension alters the accessibility of the signal peptide to SRP and TF and promotes post-translational export by reducing the efficiency of the interaction between the signal peptide and the SecYEG complex. Based on data, we propose that the N-terminal extension mediates an interaction with an unidentified cytoplasmic factor or induces the formation of an unusual signal peptide conformation prior to the onset of protein translocation.     

Exploiting beach filling as an unaffordable experiment: Benthic intertidal impacts propagating upwards to shorebirds

Cold-season filling using much coarser sediments than the native caused dramatic suppression of beach macroinvertebrates, demonstrably degrading habitat value for foraging shorebirds. As a dual consequence of persistent steepening of the foreshore, which translated to reduction in habitat area by 14-29%, and disturbance-induced depression of invertebrate densities on filled beaches, abundances of Donax spp. and haustoriid amphipods averaged less than 10% of control levels. Donax spp. is the biomass dominant and a key prey for higher trophic levels. Haustoriids lack pelagic larvae. Recovery on filled beaches was not initiated by either taxon during the March-November sampling. Emerita talpoida, an order of magnitude less abundant than Donax spp. on control beaches, exhibited a pattern of initial depression on filled beaches but recovered by mid summer. Polychaetes, mostly the small Scolelepis squamata, experienced a warm-season bloom of equal magnitude on filled and control beaches. Summertime recruitment of predatory ghost crabs appeared inhibited on filled beaches, perhaps by persistent shell hash. Intertidal shell cover on filled beaches averaged 25-50% in mid summer as compared to 6-8% on control beaches. Largely in response to prey depression, but perhaps also to surface shell armoring and/or coarsening of sediments, shorebird (mostly sanderling) use plummeted by 70-90% on filled beaches until November. Thus, despite likely adaptations to natural sediment dynamics, the high intensity of sediment deposition, cumulative spatial scope (10.8 km), and unnaturally coarse shelly character of the Bogue Banks beach nourishment resulted in a perturbation that exceeded biotic resistance and degraded the trophic transfer function of this highly productive habitat for at least one warm season.