γ-PGA Hydrolases of Phage Origin in Bacillus subtilis and Other Microbial Genomes.
γ-PGA Hydrolases of Phage Origin in Bacillus subtilis and Other Microbial Genomes.
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DOI:
10.1371/journal.pone.0130810
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发表时间:
2015
期刊:
影响因子:
3.7
通讯作者:
Calvio C
中科院分区:
文献类型:
--
作者:
Mamberti S;Prati P;Cremaschi P;Seppi C;Morelli CF;Galizzi A;Fabbi M;Calvio C
Poly-γ-glutamate (γ-PGA) is an industrially interesting polymer secreted mainly by members of the class Bacilli which forms a shield able to protect bacteria from phagocytosis and phages. Few enzymes are known to degrade γ-PGA; among them is a phage-encoded γ-PGA hydrolase, PghP. The supposed role of PghP in phages is to ensure access to the surface of bacterial cells by dismantling the γ-PGA barrier. We identified four unannotated B. subtilis genes through similarity of their encoded products to PghP; in fact these genes reside in prophage elements of B. subtilis genome. The recombinant products of two of them demonstrate efficient polymer degradation, confirming that sequence similarity reflects functional homology. Genes encoding similar γ-PGA hydrolases were identified in phages specific for the order Bacillales and in numerous microbial genomes, not only belonging to that order. The distribution of the γ-PGA biosynthesis operon was also investigated with a bioinformatics approach; it was found that the list of organisms endowed with γ-PGA biosynthetic functions is larger than expected and includes several pathogenic species. Moreover in non-Bacillales bacteria the predicted γ-PGA hydrolase genes are preferentially found in species that do not have the genetic asset for polymer production. Our findings suggest that γ-PGA hydrolase genes might have spread across microbial genomes via horizontal exchanges rather than via phage infection. We hypothesize that, in natural habitats rich in γ-PGA supplied by producer organisms, the availability of hydrolases that release glutamate oligomers from γ-PGA might be a beneficial trait under positive selection.
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DOI:
10.1107/s1744309109029881
发表时间:
2009-09-01
影响因子:
0.9
作者:
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通讯作者:
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影响因子:
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通讯作者:
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DOI:
10.1107/s1744309110001685
发表时间:
2010-10-01
影响因子:
0.9
作者:
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通讯作者:
Finn, Robert D.