Horizontal-Acquisition of a Promiscuous Peptidoglycan-Recycling Enzyme Enables Aphids To Influence Symbiont Cell Wall Metabolism
| العنوان: | Horizontal-Acquisition of a Promiscuous Peptidoglycan-Recycling Enzyme Enables Aphids To Influence Symbiont Cell Wall Metabolism |
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| المؤلفون: | Thomas E. Smith, Mijoon Lee, Maria D. Person, Dusan Hesek, Shahriar Mobashery, Nancy A. Moran |
| المصدر: | mBio mBio, Vol 12, Iss 6 (2021) |
| سنة النشر: | 2021 |
| مصطلحات موضوعية: | Gene Transfer, Horizontal, enzyme promiscuity, food and beverages, N-Acetylmuramoyl-L-alanine Amidase, Peptidoglycan, pea aphid, biochemical phenomena, metabolism, and nutrition, Microbiology, QR1-502, symbiosis, carboxypeptidase, Bacterial Proteins, Buchnera, Cell Wall, Virology, Aphids, Animals, Insect Proteins, horizontal gene transfer, multifunctional, endopeptidase, Research Article |
| الوصف: | During evolution, enzymes can undergo shifts in preferred substrates or in catalytic activities. An intriguing question is how enzyme function changes following horizontal gene transfer, especially for bacterial genes that have moved to animal genomes. Some insects have acquired genes that encode enzymes for the biosynthesis of bacterial cell wall components and that appear to function to support or control their obligate endosymbiotic bacteria. In aphids, the bacterial endosymbiont Buchnera aphidicola provides essential amino acids for aphid hosts but lacks most genes for remodeling of the bacterial cell wall. The aphid genome has acquired seven genes with putative functions in cell wall metabolism that are primarily expressed in the aphid cells harboring Buchnera. In analyses of aphid homogenates, we detected peptidoglycan (PGN) muropeptides indicative of the reactions of PGN hydrolases encoded by horizontally acquired aphid genes but not by Buchnera genes. We produced one such host enzyme, ApLdcA, and characterized its activity with both cell wall derived and synthetic PGN. Both ApLdcA and the homologous enzyme in Escherichia coli, which functions as an l,d-carboxypeptidase in the cytoplasmic PGN recycling pathway, exhibit turnover of PGN substrates containing stem pentapeptides and cross-linkages via l,d-endopeptidase activity, consistent with a potential role in cell wall remodeling. Our results suggest that ApLdcA derives its functions from the promiscuous activities of an ancestral LdcA enzyme, whose acquisition by the aphid genome may have enabled hosts to influence Buchnera cell wall metabolism as a means to control symbiont growth and division. IMPORTANCE Most enzymes are capable of performing biologically irrelevant side reactions. During evolution, promiscuous enzyme activities may acquire new biological roles, especially after horizontal gene transfer to new organisms. Pea aphids harbor obligate bacterial symbionts called Buchnera and encode horizontally acquired bacterial genes with putative roles in cell wall metabolism. Though Buchnera lacks cell wall endopeptidase genes, we found evidence of endopeptidase activity among peptidoglycan muropeptides purified from aphids. We characterized a multifunctional, aphid-encoded enzyme, ApLdcA, which displays l,d-endopeptidase activities considered promiscuous for the Escherichia coli homolog, for which these activities do not contribute to its native role in peptidoglycan recycling. These results exemplify the roles of enzyme promiscuity and horizontal gene transfer in enzyme evolution and demonstrate how aphids influence symbiont cell wall metabolism. |
| تدمد: | 2150-7511 |
| URL الوصول: | https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c32e17b4dd3f89eda08ee8209c38e183 https://pubmed.ncbi.nlm.nih.gov/34933456 |
| حقوق: | OPEN |
| رقم الأكسشن: | edsair.doi.dedup.....c32e17b4dd3f89eda08ee8209c38e183 |
| قاعدة البيانات: | OpenAIRE |
| تدمد: | 21507511 |
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