TY - JOUR
T1 - A LysM Domain intervenes in sequential protein-protein and protein-peptidoglycan interactions important for spore coat assembly in bacillus subtilis
AU - Pereira, Fatima C.
AU - Nunes, Filipa
AU - Cruz, Fernando
AU - Fernandes, Catarina
AU - Isidro, Anabela L.
AU - Lousa, Diana
AU - Soares, Cláudio M.
AU - Moran, Charles P.
AU - Henriques, Adriano O.
AU - Serrano, Mónica
PY - 2019/2/1
Y1 - 2019/2/1
N2 -
At a late stage in spore development in Bacillus subtilis, the mother cell directs synthesis of a layer of peptidoglycan known as the cortex between the two forespore membranes, as well as the assembly of a protective protein coat at the surface of the forespore outer membrane. SafA, the key determinant of inner coat assembly, is first recruited to the surface of the developing spore and then encases the spore under the control of the morphogenetic protein SpoVID. SafA has a LysM peptidoglycan-binding domain, SafA
LysM
, and localizes to the cortex-coat interface in mature spores. SafA
LysM
is followed by a region, A, required for an interaction with SpoVID and encasement. We now show that residues D10 and N30 in SafA
LysM
, while involved in the interaction with peptidoglycan, are also required for the interaction with SpoVID and encasement. We further show that single alanine substitutions on residues S11, L12, and I39 of SafA
LysM
that strongly impair binding to purified cortex peptidoglycan affect a later stage in the localization of SafA that is also dependent on the activity of SpoVE, a transglycosylase required for cortex formation. The assembly of SafA thus involves sequential protein-protein and protein-peptidoglycan interactions, mediated by the LysM domain, which are required first for encasement then for the final localization of the protein in mature spores. IMPORTANCE Bacillus subtilis spores are encased in a multiprotein coat that surrounds an underlying peptidoglycan layer, the cortex. How the connection between the two layers is enforced is not well established. Here, we elucidate the role of the peptidoglycan-binding LysM domain, present in two proteins, SafA and SpoVID, that govern the localization of additional proteins to the coat. We found that SafA
LysM
is a protein-protein interaction module during the early stages of coat assembly and a cortex-binding module at late stages in morphogenesis, with the cortex-binding function promoting a tight connection between the cortex and the coat. In contrast, SpoVID
LysM
functions only as a protein-protein interaction domain that targets SpoVID to the spore surface at the onset of coat assembly.
AB -
At a late stage in spore development in Bacillus subtilis, the mother cell directs synthesis of a layer of peptidoglycan known as the cortex between the two forespore membranes, as well as the assembly of a protective protein coat at the surface of the forespore outer membrane. SafA, the key determinant of inner coat assembly, is first recruited to the surface of the developing spore and then encases the spore under the control of the morphogenetic protein SpoVID. SafA has a LysM peptidoglycan-binding domain, SafA
LysM
, and localizes to the cortex-coat interface in mature spores. SafA
LysM
is followed by a region, A, required for an interaction with SpoVID and encasement. We now show that residues D10 and N30 in SafA
LysM
, while involved in the interaction with peptidoglycan, are also required for the interaction with SpoVID and encasement. We further show that single alanine substitutions on residues S11, L12, and I39 of SafA
LysM
that strongly impair binding to purified cortex peptidoglycan affect a later stage in the localization of SafA that is also dependent on the activity of SpoVE, a transglycosylase required for cortex formation. The assembly of SafA thus involves sequential protein-protein and protein-peptidoglycan interactions, mediated by the LysM domain, which are required first for encasement then for the final localization of the protein in mature spores. IMPORTANCE Bacillus subtilis spores are encased in a multiprotein coat that surrounds an underlying peptidoglycan layer, the cortex. How the connection between the two layers is enforced is not well established. Here, we elucidate the role of the peptidoglycan-binding LysM domain, present in two proteins, SafA and SpoVID, that govern the localization of additional proteins to the coat. We found that SafA
LysM
is a protein-protein interaction module during the early stages of coat assembly and a cortex-binding module at late stages in morphogenesis, with the cortex-binding function promoting a tight connection between the cortex and the coat. In contrast, SpoVID
LysM
functions only as a protein-protein interaction domain that targets SpoVID to the spore surface at the onset of coat assembly.
KW - LysM domain
KW - Peptidoglycan-binding protein
KW - Spore coat
KW - Spore cortex
KW - Sporulation
KW - SpoVID
UR - http://www.scopus.com/inward/record.url?scp=85061486186&partnerID=8YFLogxK
U2 - 10.1128/JB.00642-18
DO - 10.1128/JB.00642-18
M3 - Article
C2 - 30455281
AN - SCOPUS:85061486186
SN - 0021-9193
VL - 201
JO - Journal of Bacteriology
JF - Journal of Bacteriology
IS - 4
M1 - e00642-18
ER -