Genetic Analysis of the γ-Aminobutyrate Utilization Pathway in Escherichia coli K-12

The control mutation that results in a concomitant severalfold increase in the activities of gamma-aminobutyrate-alpha-ketoglutarate transaminase (GSST, EC 2.6.1.19) and succinic semialdehyde dehydrogenase (SSDH, EC 1.2.1.16), leading to the acquisition of the ability to utilize gamma-aminobutyrate (GABA) as the sole source of nitrogen by Escherichia coli K-12 mutants, was mapped by mating and transduction with P1kc. The locus affected, gabC, is approximately 48% co-transduced with the thyA gene, located at min 55 of the E. coli K-12 chromosome. The structural gene of the first enzyme in the GABA pathway, GSST, was mapped by interrupted mating, using one of the GSST-less mutants, DB742, isolated in this work. The mutated locus, gabT, is situated at about min 73 of the E. coli chromosome, close to the gltC gene. Genetic evidence concerning the sensitivity of the enzymes of the GABA pathway to catabolite repression under different physiological conditions suggests that the two structural genes of the GABA regulon do not constitute one operon.     

Modulation of a human immunosuppressive lymphokine by monosaccharides

Soluble suppressor factor (SSF) is a recently purified human lymphokine produced by peripheral blood lymphocytes (PBL) in serum-free medium as a likely consequence of an autologous mixed lymphocyte reaction. Immunoregulatory actions of SSF include suppression of: polyclonal B cell activation, proliferative responses of normal PBL, and natural killer (NK) and antibody-dependent cellular cytotoxicity. We examined the ability of the monosaccharides fucose (Fuc), galactose (Gal), glucose (Glc), and mannose (Man) to reverse SSF-mediated suppression of NK activity. Fuc and Gal can partially or completely reverse SSF-mediated suppression at four effector:target cell ratios. Man and Glc were unable to significantly reverse SSF-mediated suppression. Fuc or Gal was added to PBL at various times after addition of SSF. SSF-mediated suppression of NK cytotoxicity becomes irreversible with respect to these monosaccharides during the first 24 hr of PBL exposure to SSF. To explore the mechanism behind this block of SSF-mediated suppression. Fuc or Gal (50 mM) was cultured with PBL for 24 hr before addition of SSF, or with SSF for 24 hr before addition to PBL. Our experiments indicate that SSF is directly interacting with these monosaccharides, and may function by recognizing specific sugar moieties on the surface of effector cells.     

Orthonasal and Retronasal Odorant Identification Based upon Vapor Phase Input from Common Substances

Subjects were trained to identify by assigned number commonsubstances presented as vapor phase stimuli via an orthonasalor a retronasal route. Following training, odorant identificationlearning was evaluated by measuring ability to correctly identifyto a criterion. Those who met the criterion were then testedfirst with the stimuli presented to the nares that differedin location from the nares used in training, and second to thenares that corresponded in location to the nares used in training.It was found that, under conditions of natural retronasal breathing,orthonasally trained subjects made correct identifications on{small tilde}80% of the trials upon retronasal testing, butfor the following orthonasal testing identifications were significantlymore frequent, approaching 100% correct. After subsequent retronasaltraining, the same subjects' orthonasal identifications remainedsignificantly higher, although identifications improved to {smalltilde}92% correct on retronasal trials. Other subjects wereinstructed in a breathing technique designed to enhance retronasalstimulation. After orthonasal training, retronasal testing ofthese subjects still gave significantly fewer correct identificationsthan orthonasal testing, notwithstanding the modified retronasalbreathing, but after subsequent retronasal training correctidentifications by these subjects no longer differed significantlybetween orthonasal and retronasal testing. Efficacy of modifiedretronasal breathing was confirmed in two subsequent experiments.The observed substantial positive transfers between retronasaland orthonasal odorant identification training and testing locidemonstrate that these odorant pathways do not subserve completelyindependent olfactory systems, while the less accurate identificationsvia the retronasal route, unless instruction in retronasal breathingwas given, suggest a difference in the efficiency with whichodorants are normally delivered to the olfactory mucosa. Chem.Senses 21: 529–543, 1996.     

A gastropod’s induced behavioral and morphological responses to invasive Carcinus maenas in Australia indicate a lack of novelty advantage

Evolution has afforded many organisms the capacity to recognize predation threats and respond accordingly with behavioral and morphological defenses. Biological invasions may obviate these coevolved recognition systems resulting in biological interactions with native species that range from novelty advantages to disadvantages for the introduced species. Predator recognition initiates responses that can affect other community members through trait-mediated indirect interactions. In this study we use the Australian invasion of a marine, predatory crab (Carcinus maenas) to determine if populations of a native whelk (Haustrum vinosum) with different histories of Carcinus invasion (no previous exposure, 20 years of exposure and 100 years of exposure) recognize and respond to the introduced crab. Haustrum were subsampled from invaded and uninvaded populations then monitored for foraging behavior, shell growth and tissue growth while maintained in a common garden setting with and without waterborne cues from Carcinus. We found that both invaded and uninvaded populations of Haustrum recognize and respond to Carcinus by reducing shell growth and foraging. In feeding experiments, Carcinus showed a preference for small whelks but not thin-shelled whelks. Our results suggest that introduced populations of Carcinus in Australia do not benefit from a novelty advantage and that the induced morphological changes in Haustrum are not a defense, per se. Haustrum’s induced behavioral response to Carcinus may be more important in reducing predation than morphological defenses, and further propagate the invasive crab’s impacts.     

Serum effects confound the neuroleptic radioreceptor assay

The neuroleptic radioreceptor assay (NRRA) is used widely to monitor total neuroleptic-like activity (NLA) in patients taking one or more antipsychotic drugs. The original report of Creese and Snyder (1) stated that serum alone caused a small effect on binding which was negligible compared to normal daily variations in the assay. Conversely, in studies with striata from rat or cow brain, we found that sera from healthy, drug free volunteers, when used at 50 microL/1 mL assay volume, caused marked inhibition of binding. Although any sample of serum causes reproducible inhibition with a given preparation of bovine or rat striatal membranes, the effects of various serum samples may differ markedly when several striatal membrane preparations are compared. Moreover, samples taken from people at different times may also vary, although less than the interindividual differences. Despite this variance, the slopes of log-logit plots were equal to 1 either in the presence or absence of serum. Because of the differences in the interaction of individual sera with different membrane preparations, it is difficult to compensate accurately for this serum effect by simply including control serum in the standard curve. Thus, the use of the NRRA as a quantitative tool in the clinical pharmacology of neuroleptics may be limited by this non-specific effect of serum, and this finding may offer one explanation for some of the inconsistencies found in comparing the NRRA with direct analytical methods.