| Title : Lipolytic enzymes in Myxococcus xanthus - Moraleda-Munoz_2007_J.Bacteriol_189_3072 |
| Author(s) : Moraleda-Munoz A , Shimkets LJ |
| Ref : Journal of Bacteriology , 189 :3072 , 2007 |
|
Abstract :
The genome of Myxococcus xanthus encodes lipolytic enzymes in three different families: patatin lipases, alpha/beta hydrolases, and GDSL lipases. One member of each family was characterized. The protein encoded by MXAN_3852 contains motifs characteristic of patatins. MXAN_5522 encodes a protein with the G-X-S-X-G motif characteristic of the lipase subfamily of alpha/beta hydrolases. MXAN_4569 encodes a member of the GDSL family of lipolytic enzymes. Strains with deletions of MXAN_5522 and MXAN_4569 undergo faster development and earlier myxospore formation than the wild-type strain. The MXAN_5522 mutation results in spore yields substantially higher than those seen for wild-type cells. Gene expression analysis using translational lacZ fusions indicates that while all three genes are expressed during development, only MXAN_5522 and MXAN_4569 are expressed during vegetative growth. The proteins encoded by these genes were overexpressed using a T7 RNA polymerase transcription (pET102/D-TOPO) system in Escherichia coli BL21 Star (DE3) cells. The substrate specificities of the purified enzymes were investigated using p-nitrophenyl esters with chain lengths from C(2) to C(16). These enzymes preferentially hydrolyzed esters of short-chain fatty acids, yielding the highest activity with p-nitrophenyl acetate. |
| PubMedSearch : Moraleda-Munoz_2007_J.Bacteriol_189_3072 |
| PubMedID: 17307851 |
Moraleda-Munoz A, Shimkets LJ (2007)
Lipolytic enzymes in Myxococcus xanthus
Journal of Bacteriology
189 :3072
Moraleda-Munoz A, Shimkets LJ (2007)
Journal of Bacteriology
189 :3072