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| Auteurs principaux: | , , , , , , |
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| Format: | Artículo científico |
| Langue: | en |
| Publié: |
Molecular biology of the cell
2025
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| Sujets: | |
| Accès en ligne: | https://pubmed.ncbi.nlm.nih.gov/40105931/ |
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| _version_ | 1868266228856913921 |
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| author | Henthorn, Daniel Wilson, Sean Tank, Raveen K Mallard, William Fadero, Tanner Gao, Ruixuan Garner, Ethan C |
| author_facet | Henthorn, Daniel Wilson, Sean Tank, Raveen K Mallard, William Fadero, Tanner Gao, Ruixuan Garner, Ethan C Henthorn, Daniel Wilson, Sean Tank, Raveen K Mallard, William Fadero, Tanner Gao, Ruixuan Garner, Ethan C |
| collection | PubMed - marine biology |
| contents | twisting arises from torsional stress established by cell wall insertion and released by hydrolase-mediated cell wall cleavage. Henthorn, Daniel Wilson, Sean Tank, Raveen K Mallard, William Fadero, Tanner Gao, Ruixuan Garner, Ethan C Bacillus subtilis Cell Wall Hydrolases Bacterial Proteins Escherichia coli Peptidoglycan The cell walls of rod-shaped Gram-positive bacteria are thick, multilayered networks that chirally twist as cells elongate. The underlying basis of twisting is not known, but probing the processes underlying this phenomenon may give insights into how cell wall material is inserted, how it evolves during cleavage, and the mechanics within the sacculus. In , we see cell chains lacking hydrolases twist far slower than chains of wild-type cells, indicating that cell wall cleavage modulates the twisting rate. We see that when cells within chains separate, the two nascent ends rotate as they separate. Together, this suggests there is torsional stress within the cell wall that, when unreleased, perturbs overall chain morphology. Unlike , we see that twisting does not arise from MreB's angle of motion, as its angle is identical in both fast-twisting wild-type cells and slow-twisting hydrolase-deficient cells. Rather, the circumferential insertion of glycans appears to establish this torsional stress, as increasing Rod complex activity by deleting causes cells to twist faster than wild-type cells. Together, these experiments suggest the twisting of cells arises from radial glycan insertion, which somehow causes torsional stress in the wall that is later released by hydrolase activity. |
| format | Artículo científico |
| id | pubmed_40105931 |
| institution | PubMed |
| language | en |
| publishDate | 2025 |
| publisher | Molecular biology of the cell |
| record_format | pubmed |
| spellingShingle | twisting arises from torsional stress established by cell wall insertion and released by hydrolase-mediated cell wall cleavage. Henthorn, Daniel Wilson, Sean Tank, Raveen K Mallard, William Fadero, Tanner Gao, Ruixuan Garner, Ethan C Bacillus subtilis Cell Wall Hydrolases Bacterial Proteins Escherichia coli Peptidoglycan twisting arises from torsional stress established by cell wall insertion and released by hydrolase-mediated cell wall cleavage. Henthorn, Daniel Wilson, Sean Tank, Raveen K Mallard, William Fadero, Tanner Gao, Ruixuan Garner, Ethan C Bacillus subtilis Cell Wall Hydrolases Bacterial Proteins Escherichia coli Peptidoglycan The cell walls of rod-shaped Gram-positive bacteria are thick, multilayered networks that chirally twist as cells elongate. The underlying basis of twisting is not known, but probing the processes underlying this phenomenon may give insights into how cell wall material is inserted, how it evolves during cleavage, and the mechanics within the sacculus. In , we see cell chains lacking hydrolases twist far slower than chains of wild-type cells, indicating that cell wall cleavage modulates the twisting rate. We see that when cells within chains separate, the two nascent ends rotate as they separate. Together, this suggests there is torsional stress within the cell wall that, when unreleased, perturbs overall chain morphology. Unlike , we see that twisting does not arise from MreB's angle of motion, as its angle is identical in both fast-twisting wild-type cells and slow-twisting hydrolase-deficient cells. Rather, the circumferential insertion of glycans appears to establish this torsional stress, as increasing Rod complex activity by deleting causes cells to twist faster than wild-type cells. Together, these experiments suggest the twisting of cells arises from radial glycan insertion, which somehow causes torsional stress in the wall that is later released by hydrolase activity. |
| title | twisting arises from torsional stress established by cell wall insertion and released by hydrolase-mediated cell wall cleavage. |
| topic | Bacillus subtilis Cell Wall Hydrolases Bacterial Proteins Escherichia coli Peptidoglycan |
| url | https://pubmed.ncbi.nlm.nih.gov/40105931/ |