Regulated Control of the Assembly and Diversity of LPS by Noncoding sRNAs - Publication - Bridge of Knowledge

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Regulated Control of the Assembly and Diversity of LPS by Noncoding sRNAs

Abstract

The outer membrane (OM) of Gram-negative bacteria is asymmetric due to the presence of lipopolysaccharide (LPS) facing the outer leaflet of the OM and phospholipids facing the periplasmic side. LPS is essential for bacterial viability, since it provides a permeability barrier and is a major virulence determinant in pathogenic bacteria. In Escherichia coli, several steps of LPS biosynthesis and assembly are regulated by the RpoE sigma factor and stress responsive two-component systems as well as dedicated small RNAs. LPS composition is highly heterogeneous and dynamically altered upon stress and other challenges in the environment because of the transcriptional activation of RpoE regulon members and posttranslational control by RpoE-regulated Hfq-dependent RybB and MicA sRNAs. The PhoP/Q two-component system further regulates Kdo2-lipid A modification via MgrR sRNA. Some of these structural alterations are critical for antibiotic resistance, OM integrity, virulence, survival in host, and adaptation to specific environmental niches. The heterogeneity arises following the incorporation of nonstoichiometric modifications in the lipid A part and alterations in the composition of inner and outer core of LPS. The biosynthesis of LPS and phospholipids is tightly coupled. This requires the availability of metabolic precursors, whose accumulation is controlled by sRNAs like SlrA, GlmZ, and GlmY.

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DOI:
Digital Object Identifier (open in new tab) 10.1155/2015/153561
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Category:
Articles
Type:
artykuł w czasopiśmie wyróżnionym w JCR
Published in:
JOURNAL OF BIOMEDICINE AND BIOTECHNOLOGY no. 2015, pages 1 - 16,
ISSN: 1110-7243
Language:
English
Publication year:
2015
Bibliographic description:
Klein-Raina G., Raina S.: Regulated Control of the Assembly and Diversity of LPS by Noncoding sRNAs// JOURNAL OF BIOMEDICINE AND BIOTECHNOLOGY. -Vol. 2015, (2015), s.1-16
DOI:
Digital Object Identifier (open in new tab) 10.1155/2015/153561
Verified by:
Gdańsk University of Technology

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