| Literature DB >> 31653338 |
Eaazhisai Kandiah1, Diego Carriel2, Pierre Simon Garcia3, Jan Felix1, Manuel Banzhaf4, George Kritikos4, Maria Bacia-Verloop1, Céline Brochier-Armanet3, Sylvie Elsen5, Irina Gutsche6.
Abstract
The only enzyme responsible for cadaverine production in the major multidrug-resistant human pathogen Pseudomonas aeruginosa is the lysine decarboxylase LdcA. This enzyme modulates the general polyamine homeostasis, promotes growth, and reduces bacterial persistence during carbenicillin treatment. Here we present a 3.7-Å resolution cryoelectron microscopy structure of LdcA. We introduce an original approach correlating phylogenetic signal with structural information and reveal possible recombination among LdcA and arginine decarboxylase subfamilies within structural domain boundaries. We show that LdcA is involved in full virulence in an insect pathogenesis model. Furthermore, unlike its enterobacterial counterparts, LdcA is regulated neither by the stringent response alarmone ppGpp nor by the AAA+ ATPase RavA. Instead, the P. aeruginosa ravA gene seems to play a defensive role. Altogether, our study identifies LdcA as an important player in P. aeruginosa physiology and virulence and as a potential drug target.Entities:
Keywords: LdcA; Pseudomonas aeruginosa; amino acid decarboxylases; bacteria; cryo-EM structure; defense island; evolution; phylogenetic analysis; ppGpp; virulence
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Year: 2019 PMID: 31653338 DOI: 10.1016/j.str.2019.10.003
Source DB: PubMed Journal: Structure ISSN: 0969-2126 Impact factor: 5.006