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In vitro high-resolution structural dynamics of single germinating bacterial spores
Proceedings of the National Academy of Sciences

The high-resolution architecture and structural dynamics of Bacillus spores
Biophysical Journal, January 2005

Architecture and high-resolution structure of Bacillus thuringiensis and Bacillus cereus spore coat surfaces
Langmuir 2005
 

Public Affairs : Newsroom : News Releases : 2007 News Release Archive :: NR-07-06-01

News Release                               Printer-Friendly

  Contact: Anne M. Stark
  Phone: (925) 422-9799
  E-mail: stark8@llnl.gov
  FOR IMMEDIATE RELEASE
June 4, 2007
NR-07-06-01

Researchers track how spores break out
of dormant state

LIVERMORE, Calif. – Tapping into the unknown world of awakening dormant bacterial spores, researchers have revealed through atomic force microscopy (AFM) the alterations of spore coat and germ cell wall that accompany the transformation from a spore to a vegetative cell.

spore progression
Emergence of vegetative cells: 60- to 70-nm-deep apertures in the rodlet layer that gradually enlarged (C and D), and subsequently eroded the entire spore coat (E). Germ cells emerged from these apertures.
Click for high-resolution image

When starved of nutrients Bacillus (rod-shaped bacteria) cells initiate a series of genetic, biochemical and structural events that result in the formation of metabolically dormant spores.

They can remain dormant for extended periods and, partly because of their tough spore coat, have a significant resistance to extreme environmental factors including heat, radiation and toxic chemicals. However, once in favorable conditions, spores break the dormant state through germination and reenter the vegetative mode of replication.

Although significant progress has been made in understanding the biochemical and genetic bases of the spore germination process, it is still unclear how a spore breaks out of its dormant state.

But a new in vitro study of single germinating Bacillus atrophaeus spores details how the spore coat structures break down, and it shows with unprecedented resolution how the new bacterium emerges from the disintegrating spore.

The new research, led by Lawrence Livermore National Laboratory scientists, appears in the June 4 issue of the Proceedings of the National Academy of Sciences.

“A thorough understanding of spore germination is important for the development of new countermeasures that identify the earliest stages of a wide range of spore mediated diseases, including botulism, gas gangrene and pulmonary anthrax,” said Alexander Malkin, senior author from LLNL’s Biosciences and Biotechnology Division.

“But it’s also important to gain fundamental insights into the key events in bacterial cell development.”

spores
Atomic force microscope (AFM) images of the rodlet layer of an intact spore (top), a degrading rodlet layer during germination (middle) and the cell wall structure of the newly emerging vegetative cell (bottom)
Click for high resolution image

The researchers, including Marco Plomp, lead author at LLNL, and those from Children’s Hospital Oakland Research Institute and Northwestern University, used AFM to identify disassembly of the outer spore coat rodlet structures, which appear to be structurally similar to amyloid fibrils that have been associated with neural degenerative diseases, such as Alzheimer’s and prion diseases.

“The extreme physical and chemical resistance of Bacillus spores suggests that evolutionary forces have captured the mechanical rigidity and resistance of these amyloid self-assembling biomaterials to structure the protective outer spore surface,” Plomp said.

When exposed to a solution that triggers germination, nanometer sized etch pits were seen developing in the rodlet layer. These etch pits evolved into ever widening fissures, leaving narrow strips of remaining rodlet structure. In the end, 1- to 3- nm-wide fibrils remained. The in vitro AFM imaging also revealed the porous fibrous cell wall structure of newly emerging and mature vegetative cells, consisting of a network of nanometer-wide peptidoglycan fibers.

“These results show that dynamic AFM is a promising tool to investigate the formation and evolution of the bacterial cell wall,” Malkin said.

The research is funded by LLNL’s Laboratory Directed Research and Development program, the Defense Advanced Research Project Agency (DARPA) and the Federal Bureau of Investigation.

Founded in 1952, Lawrence Livermore National Laboratory is a national security laboratory, with a mission to ensure national security and apply science and technology to the important issues of our time. Lawrence Livermore National Laboratory is managed by the University of California for the U.S. Department of Energy’s National Nuclear Security Administration.

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October 5, 2007

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