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Autolysis of Lactococcus lactis is increased upon D-alanine depletion of peptidoglycan and lipoteichoic acids.

Steen A, Palumbo E, Deghorain M, Cocconcelli PS, Delcour J, Kuipers OP, Kok J, Buist G, Hols P.

J Bacteriol. 2005 Jan;187(1):114-24.


Reduced lysis upon growth of Lactococcus lactis on galactose is a consequence of decreased binding of the autolysin AcmA.

Steen A, Buist G, Kramer NE, Jalving R, Benus GF, Venema G, Kuipers OP, Kok J.

Appl Environ Microbiol. 2008 Aug;74(15):4671-9. doi: 10.1128/AEM.00103-08. Epub 2008 Jun 6.


Peptidoglycan N-acetylglucosamine deacetylation decreases autolysis in Lactococcus lactis.

Meyrand M, Boughammoura A, Courtin P, Mézange C, Guillot A, Chapot-Chartier MP.

Microbiology. 2007 Oct;153(Pt 10):3275-85.


Autolysis of Lactococcus lactis is influenced by proteolysis.

Buist G, Venema G, Kok J.

J Bacteriol. 1998 Nov;180(22):5947-53.


AcmD, a homolog of the major autolysin AcmA of Lactococcus lactis, binds to the cell wall and contributes to cell separation and autolysis.

Visweswaran GR, Steen A, Leenhouts K, Szeliga M, Ruban B, Hesseling-Meinders A, Dijkstra BW, Kuipers OP, Kok J, Buist G.

PLoS One. 2013 Aug 8;8(8):e72167. doi: 10.1371/journal.pone.0072167. eCollection 2013.


Autolysis of Lactococcus lactis caused by induced overproduction of its major autolysin, AcmA.

Buist G, Karsens H, Nauta A, van Sinderen D, Venema G, Kok J.

Appl Environ Microbiol. 1997 Jul;63(7):2722-8.


Requirement of autolytic activity for bacteriocin-induced lysis.

Martínez-Cuesta MC, Kok J, Herranz E, Peláez C, Requena T, Buist G.

Appl Environ Microbiol. 2000 Aug;66(8):3174-9.


AcmA of Lactococcus lactis is an N-acetylglucosaminidase with an optimal number of LysM domains for proper functioning.

Steen A, Buist G, Horsburgh GJ, Venema G, Kuipers OP, Foster SJ, Kok J.

FEBS J. 2005 Jun;272(11):2854-68.


A novel type of peptidoglycan-binding domain highly specific for amidated D-Asp cross-bridge, identified in Lactobacillus casei bacteriophage endolysins.

Regulski K, Courtin P, Kulakauskas S, Chapot-Chartier MP.

J Biol Chem. 2013 Jul 12;288(28):20416-26. doi: 10.1074/jbc.M112.446344. Epub 2013 Jun 3.


Influence of lipoteichoic acid D-alanylation on protein secretion in Lactococcus lactis as revealed by random mutagenesis.

Nouaille S, Commissaire J, Gratadoux JJ, Ravn P, Bolotin A, Gruss A, Le Loir Y, Langella P.

Appl Environ Microbiol. 2004 Mar;70(3):1600-7.


Incorporation of D-alanine into lipoteichoic acid and wall teichoic acid in Bacillus subtilis. Identification of genes and regulation.

Perego M, Glaser P, Minutello A, Strauch MA, Leopold K, Fischer W.

J Biol Chem. 1995 Jun 30;270(26):15598-606.


Biosynthesis of lipoteichoic acid in Lactobacillus rhamnosus: role of DltD in D-alanylation.

Debabov DV, Kiriukhin MY, Neuhaus FC.

J Bacteriol. 2000 May;182(10):2855-64.


Cell wall attachment of a widely distributed peptidoglycan binding domain is hindered by cell wall constituents.

Steen A, Buist G, Leenhouts KJ, El Khattabi M, Grijpstra F, Zomer AL, Venema G, Kuipers OP, Kok J.

J Biol Chem. 2003 Jun 27;278(26):23874-81. Epub 2003 Apr 8.


Functional analysis of D-alanylation of lipoteichoic acid in the probiotic strain Lactobacillus rhamnosus GG.

Perea Vélez M, Verhoeven TL, Draing C, Von Aulock S, Pfitzenmaier M, Geyer A, Lambrichts I, Grangette C, Pot B, Vanderleyden J, De Keersmaecker SC.

Appl Environ Microbiol. 2007 Jun;73(11):3595-604. Epub 2007 Apr 13.


Identification of an essential gene responsible for D-Asp incorporation in the Lactococcus lactis peptidoglycan crossbridge.

Veiga P, Piquet S, Maisons A, Furlan S, Courtin P, Chapot-Chartier MP, Kulakauskas S.

Mol Microbiol. 2006 Dec;62(6):1713-24.


Increased D-alanylation of lipoteichoic acid and a thickened septum are main determinants in the nisin resistance mechanism of Lactococcus lactis.

Kramer NE, Hasper HE, van den Bogaard PT, Morath S, de Kruijff B, Hartung T, Smid EJ, Breukink E, Kok J, Kuipers OP.

Microbiology. 2008 Jun;154(Pt 6):1755-62. doi: 10.1099/mic.0.2007/015412-0.

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