Remarks on Pure Spin Connection Formulations of Gravity

In the derivation of a pure spin connection action functional for gravity two methods have been proposed. The first starts from a first order lagrangian formulation, the second from a hamiltonian formulation. In this note we show that they lead to identical results for the specific cases of pure gravity with or without a cosmological constant

Towards a path integral for the pure-spin connection formulation of gravity

A proposal for the path-integral of pure-spin-connection formulation of gravity is described, based on the two-form formulation of Capovilla et. al. It is shown that the resulting effective-action for the spin-connection, upon functional integration of the two-form field $\Sigma$ and the auxiliary matrix field $\psi$ is {\it non-polynomial}, even for the case of vanishing cosmological constant and absence of any matter couplings. Further, a diagramatic evaluation is proposed for the contribution of the matrix-field to the pure spin connection action.Comment: 8 pages in plain-TeX.-----IUCAA_TH/9

2-Form Gravity of the Lorentzian Signature

We introduce a new spinorial, BF-like action for the Einstein gravity. This is a first, up to our knowledge, 2-form action which describes the real, Lorentzian gravity and uses only the self-dual connection. In the generic case, the corresponding classical canonical theory is equivalent to the Einstein-Ashtekar theory plus the reality conditions

Identification and structural characterisation of a partially arabinosylated lipoarabinomannan variant isolated from a Corynebacterium glutamicum ubiAmutant

Arabinan polysaccharide side-chains are present in both Mycobacterium tuberculosis and Corynebacterium glutamicum in the heteropolysaccharide arabinogalactan (AG), and in M. tuberculosis in the lipoglycan, lipoarabinomannan (LAM). Herein, we show by quantitative sugar and glycosyl linkage analysis that C. glutamicum possesses a much smaller LAM version, Cg-LAM, characterised by single t-Araf residues linked to th

Topological Lattice Gravity Using Self-Dual Variables

Topological gravity is the reduction of general relativity to flat space-times. A lattice model describing topological gravity is developed starting from a Hamiltonian lattice version of B\w F theory. The extra symmetries not present in gravity that kill the local degrees of freedom in $B\wedge F$ theory are removed. The remaining symmetries preserve the geometrical character of the lattice. Using self-dual variables, the conditions that guarantee the geometricity of the lattice become reality conditions. The local part of the remaining symmetry generators, that respect the geometricity-reality conditions, has the form of Ashtekar's constraints for GR. Only after constraining the initial data to flat lattices and considering the non-local (plus local) part of the constraints does the algebra of the symmetry generators close. A strategy to extend the model for non-flat connections and quantization are discussed.Comment: 22 pages, revtex, no figure

Higgs Bosons: Intermediate Mass Range at e+e- Colliders

We elaborate on the production of the Standard Model Higgs particle at high-energy $e^+e^-$ colliders through the reaction $e^+e^- \rightarrow ZH$. Particular emphasis is put on the intermediate mass range. In addition to the signal we discuss in detail the background processes. Angular distributions which are sensitive to the spin and parity of the Higgs particle are analyzed.Comment: Standard Latex. 15 pages. 11 figures available by fax or regular mail. MAD/PH/749, DESY 93-064, UdeM-LPN-TH-93-143, NUHEP-TH-93-1

Automated glycan assembly of arabinomannan oligosaccharides from Mycobacterium tuberculosis

Arabinomannan (AM) polysaccharides are clinical biomarkers for Mycobacterium tuberculosis (MTB) infections due to their roles in the interaction with host cells and interference with macrophage activation. Collections of defined AM oligosaccharides can help to improve the understanding of these polysaccharides and the development of novel therapeutical and diagnostic agents. Automated glycan assembly (AGA) was employed to prepare the core structure of AM from MTB, containing α-(1,6)-Man, α-(1,5)-Ara, and α-(1,2)-Man linkages. The introduction of a capping step after each glycosylation and further optimized reaction conditions allowed for the synthesis of a series of oligosaccharides, ranging from hexa- to branched dodecasaccharides