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Microbiology and Molecular Biology Reviews, December 2002, p. 702-738, Vol. 66, No. 4
1092-2172/02/$04.00+0     DOI: 10.1128/MMBR.66.4.702-738.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.

Biochemistry and Comparative Genomics of SxxK Superfamily Acyltransferases Offer a Clue to the Mycobacterial Paradox: Presence of Penicillin-Susceptible Target Proteins versus Lack of Efficiency of Penicillin as Therapeutic Agent

Colette Goffin and Jean-Marie Ghuysen*

Center for Protein Engineering, Institut de Chimie, University of Liège, B-4000 Sart Tilman, Liège, Belgium

The bacterial acyltransferases of the SxxK superfamily vary enormously in sequence and function, with conservation of particular amino acid groups and all-{alpha} and {alpha}/ß folds. They occur as independent entities (free-standing polypeptides) and as modules linked to other polypeptides (protein fusions). They can be classified into three groups. The group I SxxK D,D-acyltransferases are ubiquitous in the bacterial world. They invariably bear the motifs SxxK, SxN(D), and KT(S)G. Anchored in the plasma membrane with the bulk of the polypeptide chain exposed on the outer face of it, they are implicated in the synthesis of wall peptidoglycans of the most frequently encountered (4->3) type. They are inactivated by penicillin and other ß-lactam antibiotics acting as suicide carbonyl donors in the form of penicillin-binding proteins (PBPs). They are components of a morphogenetic apparatus which, as a whole, controls multiple parameters such as shape and size and allows the bacterial cells to enlarge and duplicate their particular pattern. Class A PBP fusions comprise a glycosyltransferase module fused to an SxxK acyltransferase of class A. Class B PBP fusions comprise a linker, i.e., protein recognition, module fused to an SxxK acyltransferase of class B. They ensure the remodeling of the (4->3) peptidoglycans in a cell cycle-dependent manner. The free-standing PBPs hydrolyze D,D peptide bonds. The group II SxxK acyltransferases frequently have a partially modified bar code, but the SxxK motif is invariant. They react with penicillin in various ways and illustrate the great plasticity of the catalytic centers. The secreted free-standing PBPs, the serine ß-lactamases, and the penicillin sensors of several penicillin sensory transducers help the D,D-acyltransferases of group I escape penicillin action. The group III SxxK acyltransferases are indistinguishable from the PBP fusion proteins of group I in motifs and membrane topology, but they resist penicillin. They are referred to as Penr protein fusions. Plausible hypotheses are put forward on the roles that the Penr protein fusions, acting as L,D-acyltransferases, may play in the (3->3) peptidoglycan-synthesizing molecular machines. Shifting the wall peptidoglycan from the (4->3) type to the (3->3) type could help Mycobacterium tuberculosis and Mycobacterium leprae survive by making them penicillin resistant.

* Corresponding author. Mailing address: Center for Protein Engineering, Institut de Chimie, University of Liège, B6, B-4000 Sart Tilman, Liège, Belgium. Phone: 32 4 366.33.96/95. Fax: 32 4 366.33.64. E-mail: jmghuysen{at}ulg.ac.be.

Microbiology and Molecular Biology Reviews, December 2002, p. 702-738, Vol. 66, No. 4
1092-2172/02/$04.00+0     DOI: 10.1128/MMBR.66.4.702-738.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.



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