Purification of liver glutamate dehydrogenase by affinity precipitation and studies on its denaturation

In the presence of glutaric acid, N2,N2'-adipodihydrazido-bis(N6-carbonylmethyl-NAD+)(bis-NAD+ ) forms cross-links between molecules of glutamate dehydrogenase, resulting in precipitation. The dependence of this process on bis-NAD+ and enzyme concentration has been investigated. This procedure has been shown to be effective in the purification of glutamate dehydrogenase from rat and ox liver, and a procedure is presented in which this affinity precipitation procedure is used instead of the affinity chromatography used in an earlier method (McCarthy, A.D., Walker, J.M. and Tipton, K.F. (1980) Biochem. J. 191, 605-611). The ox liver enzyme prepared in this way had not suffered the limited proteolysis that occurs during the preparation of the enzyme by other commonly used procedures. After the purified enzyme had been denatured by treatment with urea, guanidine hydrochloride, or low pH, no recovery of activity could be demonstrated following dilution or, in the last case, dialysis.     

Vegetation establishment, succession and microsite frost disturbance on glacier forelands within patterned ground chronosequences

Aim The impact of microscale frost disturbance on vegetation colonization and successionary trends was examined within patterned ground features of Little Ice Age chronosequences. The goal was to investigate and compare vegetation response to micro‐site frost disturbance with that of previous studies done at a coarser landscape scale. Location The study sites occur on Little Ice Age glacier forelands within Jotunheimen, Norway (61°–62° N). The forelands of the glaciers Slettmarkbreen, Styggedalsbreen and Vestre Memurubreen have been well studied providing chronological controls for landscape studies. Sorted patterned ground features are found within the chronosequences, typically declining with frost intensity and disturbance with increasing terrain age. Methods Micro‐plots (8.3 × 8.3 cm) were placed at the inner borders and centres of patterned ground features. Species were identified and per cent species cover and per cent cover of life‐form category were noted. Nonparametric Kruskal–Wallis and Mann–Whitney U‐tests were used to test for differences between percent cover of life‐form categories within patterned ground features as well as to identify thresholds of successional change across the chronosequences. Results Significant relationships between life‐from groups and patterned ground positions of varying ages were deduced using nonparametric statistics. Findings were then used to discuss trends of succession within patterned ground features and across the chronosequences. Vegetation establishment occurs at the border positions of young (< 30 years) patterned ground features. With time and distance from the ice margin, vegetation encroaches inwards toward the disturbed centres. Succession within patterned ground exhibits several stages: (1) bryophytes/crusts and lichens, (2) grasses/sedges and (3) woody shrubs. The occurrence of forbs was sporadic and generally non‐significant. Main conclusions Frost disturbance in patterned ground appears to delay successional trends of vegetation communities when compared with previous studies on ‘stable’ terrain, producing micro‐site lag effects. These small patches of disturbed ground are therefore important regarding vegetation assemblages across the landscape and are unlikely to be detected at the landscape scale.     

A 44 kilodalton cell surface homodimer regulates interleukin 2 production by activated human T lymphocytes

We previously described a cell surface antigen, termed Tp44, detected by monoclonal antibody 9.3 on approximately 80% of mature human T lymphocytes. Analysis by SDS-polyacrylamide gel electrophoresis and isoelectric focusing demonstrated that this antigen consists of two identical 44 kilodalton glycopeptides that form a disulfide-linked homodimer. Competitive binding experiments showed that antibody 9.3 and an anti-CD3 antibody (64.1) recognize distinct antigenic determinants; furthermore, the binding of antibody 9.3 was unaffected by prior modulation of CD3. Thus, Tp44 has no detectable cell surface association with CD3. By itself, antibody 9.3 had no detectable effect on either IL 2 receptor expression or IL 2 release, and did not cause T cell proliferation even when monocytes were present and exogenous IL 2 was provided, indicating that binding of antibody 9.3 does not provide a primary signal for T cell activation. However, the proliferative responses of T lymphocytes activated by phytohemagglutinin, concanavalin A, or an anti-CD3 monoclonal antibody were strikingly enhanced in the presence of antibody 9.3, an effect associated with increased IL 2 receptor expression and increased IL 2 secretion. Antibody 9.3 enabled anti-CD3-Sepharose-activated T cells and anti-CD3 antibody-activated Jurkat cells to release IL 2 in the absence of monocytes. Fab fragments of antibody 9.3 had no effect on anti-CD3-induced IL 2 release by Jurkat cells, whereas F(ab')2 fragments had activity comparable to that of unmodified antibody, indicating that bivalent binding of Tp44 molecules is required for IL 2 secretion. Together, these results suggest that TP44 may function as a receptor for accessory signals in the activation of T cells.