Literature DB >> 22859568

Physical basis for the adaptive flexibility of Bacillus spore coats.

Ozgur Sahin1, Ee Hou Yong, Adam Driks, L Mahadevan.   

Abstract

Bacillus spores are highly resistant dormant cells formed in response to starvation. The spore is surrounded by a structurally complex protein shell, the coat, which protects the genetic material. In spite of its dormancy, once nutrient is available (or an appropriate physical stimulus is provided) the spore is able to resume metabolic activity and return to vegetative growth, a process requiring the coat to be shed. Spores dynamically expand and contract in response to humidity, demanding that the coat be flexible. Despite the coat's critical biological functions, essentially nothing is known about the design principles that allow the coat to be tough but also flexible and, when metabolic activity resumes, to be efficiently shed. Here, we investigated the hypothesis that these apparently incompatible characteristics derive from an adaptive mechanical response of the coat. We generated a mechanical model predicting the emergence and dynamics of the folding patterns uniformly seen in Bacillus spore coats. According to this model, spores carefully harness mechanical instabilities to fold into a wrinkled pattern during sporulation. Owing to the inherent nonlinearity in their formation, these wrinkles persist during dormancy and allow the spore to accommodate changes in volume without compromising structural and biochemical integrity. This characteristic of the spore and its coat may inspire design of adaptive materials.

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Year:  2012        PMID: 22859568      PMCID: PMC3479929          DOI: 10.1098/rsif.2012.0470

Source DB:  PubMed          Journal:  J R Soc Interface        ISSN: 1742-5662            Impact factor:   4.118


  31 in total

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Authors:  Adam Driks
Journal:  Proc Natl Acad Sci U S A       Date:  2003-03-11       Impact factor: 11.205

2.  Characterization of spoIVA, a sporulation gene involved in coat morphogenesis in Bacillus subtilis.

Authors:  S Roels; A Driks; R Losick
Journal:  J Bacteriol       Date:  1992-01       Impact factor: 3.490

3.  Characterization of the Bacillus subtilis spore morphogenetic coat protein CotO.

Authors:  D C McPherson; H Kim; M Hahn; R Wang; P Grabowski; P Eichenberger; A Driks
Journal:  J Bacteriol       Date:  2005-12       Impact factor: 3.490

4.  Muramic lactam in peptidoglycan of Bacillus subtilis spores is required for spore outgrowth but not for spore dehydration or heat resistance.

Authors:  D L Popham; J Helin; C E Costello; P Setlow
Journal:  Proc Natl Acad Sci U S A       Date:  1996-12-24       Impact factor: 11.205

5.  Bacillus anthracis and Bacillus subtilis spore surface properties and transport.

Authors:  Gang Chen; Adam Driks; Kamal Tawfiq; Michael Mallozzi; Sandip Patil
Journal:  Colloids Surf B Biointerfaces       Date:  2009-12-28       Impact factor: 5.268

6.  An unusually small gene required for sporulation by Bacillus subtilis.

Authors:  P A Levin; N Fan; E Ricca; A Driks; R Losick; S Cutting
Journal:  Mol Microbiol       Date:  1993-08       Impact factor: 3.501

7.  Cloning and characterization of a gene required for assembly of the Bacillus subtilis spore coat.

Authors:  B Beall; A Driks; R Losick; C P Moran
Journal:  J Bacteriol       Date:  1993-03       Impact factor: 3.490

8.  Structures in the cell wall that enable hygroscopic movement of wheat awns.

Authors:  Rivka Elbaum; Stanislav Gorb; Peter Fratzl
Journal:  J Struct Biol       Date:  2008-06-24       Impact factor: 2.867

9.  Mechanism of silicate binding to the bacterial cell wall in Bacillus subtilis.

Authors:  M U Mera; T J Beveridge
Journal:  J Bacteriol       Date:  1993-04       Impact factor: 3.490

10.  Unmasking novel sporulation genes in Bacillus subtilis.

Authors:  Jessica M Silvaggi; David L Popham; Adam Driks; Patrick Eichenberger; Richard Losick
Journal:  J Bacteriol       Date:  2004-12       Impact factor: 3.490

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  7 in total

Review 1.  Protein Synthesis during Germination: Shedding New Light on a Classical Question.

Authors:  Tyler Boone; Adam Driks
Journal:  J Bacteriol       Date:  2016-11-18       Impact factor: 3.490

2.  Bacillus spores as building blocks for stimuli-responsive materials and nanogenerators.

Authors:  Xi Chen; L Mahadevan; Adam Driks; Ozgur Sahin
Journal:  Nat Nanotechnol       Date:  2014-01-26       Impact factor: 39.213

3.  Nanomechanical Characterization of Bacillus anthracis Spores by Atomic Force Microscopy.

Authors:  Alex G Li; Larry W Burggraf; Yun Xing
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4.  Identifying different types of microorganisms with terahertz spectroscopy.

Authors:  S A Yoon; S H Cha; S W Jun; S J Park; J-Y Park; S Lee; H S Kim; Y H Ahn
Journal:  Biomed Opt Express       Date:  2019-12-23       Impact factor: 3.732

5.  Resilient living materials built by printing bacterial spores.

Authors:  Lina M González; Nikita Mukhitov; Christopher A Voigt
Journal:  Nat Chem Biol       Date:  2019-12-02       Impact factor: 15.040

6.  High-precision fitting measurements of the kinetics of size changes during germination of individual Bacillus spores.

Authors:  Jintao Liang; Pengfei Zhang; Peter Setlow; Yong-Qing Li
Journal:  Appl Environ Microbiol       Date:  2014-08       Impact factor: 4.792

7.  Analysis of killing of growing cells and dormant and germinated spores of Bacillus species by black silicon nanopillars.

Authors:  Sonali Ghosh; Shanyuan Niu; Maya Yankova; Matthew Mecklenburg; Stephen M King; Jayakanth Ravichandran; Rajiv K Kalia; Aiichiro Nakano; Priya Vashishta; Peter Setlow
Journal:  Sci Rep       Date:  2017-12-19       Impact factor: 4.379

  7 in total

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