Literature DB >> 10849429

Do sequence repeats play an equivalent role in the choline-binding module of pneumococcal LytA amidase?

J Varea1, J L Saiz, C López-Zumel, B Monterroso, F J Medrano, J L Arrondo, I Iloro, J Laynez, J L Garcia, M Menéndez.   

Abstract

LytA amidase breaks down the N-acetylmuramoyl-l-alanine bonds in the peptidoglycan backbone of Streptococcus pneumoniae. Its polypeptide chain has two modules: the NH(2)-terminal module, responsible for the catalytic activity, and the COOH-terminal module, constructed by six tandem repeats of 20 or 21 amino acids (p1-p6) and a short COOH-terminal tail. The polypeptide chain must contain at least four repeats to efficiently anchor the autolysin to the choline residues of the cell wall. Nevertheless, the catalytic efficiency decreases by 90% upon deletion of the final tail. The structural implications of deleting step by step the two last (p5 and p6) repeats and the final COOH-tail and their effects on choline-amidase interactions have been examined by comparing four truncated mutants with LytA amidase by means of different techniques. Removal of this region has minor effects on secondary structure content but significantly affects the stability of native conformations. The last 11 amino acids and the p5 repeat stabilize the COOH-terminal module; each increases the module transition temperature by about 6 degrees C. Moreover, the p5 motif also seems to participate, in a choline-dependent way, in the stabilization of the NH(2)-terminal module. The effects of choline binding on the thermal stability profile of the mutant lacking the p5 repeat might reflect a cooperative pathway providing molecular communication between the choline-binding module and the NH(2)-terminal region. The three sequence motives favor the choline-amidase interaction, but the tail is an essential factor in the monomer <--> dimer self-association equilibrium of LytA and its regulation by choline. The final tail is required for preferential interaction of choline with LytA dimers and for the existence of different sets of choline-binding sites. The p6 repeat scarcely affects the amidase stability but could provide the proper three-dimensional orientation of the final tail.

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Year:  2000        PMID: 10849429     DOI: 10.1074/jbc.M004379200

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  14 in total

1.  Linker Editing of Pneumococcal Lysin ClyJ Conveys Improved Bactericidal Activity.

Authors:  Hang Yang; Dehua Luo; Irina Etobayeva; Xiaohong Li; Yujing Gong; Shujuan Wang; Qiong Li; Poshi Xu; Wen Yin; Jin He; Daniel C Nelson; Hongping Wei
Journal:  Antimicrob Agents Chemother       Date:  2020-01-27       Impact factor: 5.191

2.  On the remarkable mechanostability of scaffoldins and the mechanical clamp motif.

Authors:  Alejandro Valbuena; Javier Oroz; Rubén Hervás; Andrés Manuel Vera; David Rodríguez; Margarita Menéndez; Joanna I Sulkowska; Marek Cieplak; Mariano Carrión-Vázquez
Journal:  Proc Natl Acad Sci U S A       Date:  2009-07-31       Impact factor: 11.205

3.  Unravelling the structure of the pneumococcal autolytic lysozyme.

Authors:  Begoña Monterroso; Consuelo López-Zumel; José L García; José L Sáiz; Pedro García; Nuria E Campillo; Margarita Menéndez
Journal:  Biochem J       Date:  2005-10-01       Impact factor: 3.857

4.  ClyJ Is a Novel Pneumococcal Chimeric Lysin with a Cysteine- and Histidine-Dependent Amidohydrolase/Peptidase Catalytic Domain.

Authors:  Hang Yang; Yujing Gong; Huaidong Zhang; Irina Etobayeva; Paulina Miernikiewicz; Dehua Luo; Xiaohong Li; Xiaoxu Zhang; Krystyna Dąbrowska; Daniel C Nelson; Jin He; Hongping Wei
Journal:  Antimicrob Agents Chemother       Date:  2019-03-27       Impact factor: 5.191

5.  Accumulation of partly folded states in the equilibrium unfolding of the pneumococcal choline-binding module C-LytA.

Authors:  Beatriz Maestro; Jesús M Sanz
Journal:  Biochem J       Date:  2005-04-15       Impact factor: 3.857

6.  Insights into the structure-function relationships of pneumococcal cell wall lysozymes, LytC and Cpl-1.

Authors:  Begoña Monterroso; José Luis Sáiz; Pedro García; José Luis García; Margarita Menéndez
Journal:  J Biol Chem       Date:  2008-07-30       Impact factor: 5.157

7.  A Choline-Recognizing Monomeric Lysin, ClyJ-3m, Shows Elevated Activity against Streptococcus pneumoniae.

Authors:  Dehua Luo; Li Huang; Vijay Singh Gondil; Wanli Zhou; Wan Yang; Minghui Jia; Shencai Hu; Jin He; Hang Yang; Hongping Wei
Journal:  Antimicrob Agents Chemother       Date:  2020-11-17       Impact factor: 5.191

8.  Characterization of Ejl, the cell-wall amidase coded by the pneumococcal bacteriophage Ej-1.

Authors:  José L Sáiz; Consuelo López-Zumel; Begoña Monterroso; Julio Varea; José Luis R Arrondo; Ibon Iloro; José L García; José Laynez; Margarita Menéndez
Journal:  Protein Sci       Date:  2002-07       Impact factor: 6.725

9.  Structure of pneumococcal peptidoglycan hydrolase LytB reveals insights into the bacterial cell wall remodeling and pathogenesis.

Authors:  Xiao-Hui Bai; Hui-Jie Chen; Yong-Liang Jiang; Zhensong Wen; Yubin Huang; Wang Cheng; Qiong Li; Lei Qi; Jing-Ren Zhang; Yuxing Chen; Cong-Zhao Zhou
Journal:  J Biol Chem       Date:  2014-07-07       Impact factor: 5.157

Review 10.  Listeria monocytogenes surface proteins: from genome predictions to function.

Authors:  Hélène Bierne; Pascale Cossart
Journal:  Microbiol Mol Biol Rev       Date:  2007-06       Impact factor: 11.056

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