The long-term goal of this research is to determine why bacteria undergo specific changes in morphology. Bacteria, including pathogens, are found in a vast array of morphologies;however functions have rarely been attributed to specific shapes. In this work, the function of morphological changes in bacteria with cell membrane extensions, known as stalks, will examined as a model system to study the function of morphological adaptation. Recent mathematical models suggest that in nutrient limited environments, such as those inhabited by the stalked bacteria, increasing the length of the cell (and not the surface area) is the most important factor in increasing the efficiency of nutrient uptake. This suggests that the stalk plays a predominant role in the uptake of nutrients and promotes cell growth. Indeed, phosphate limitation is known to induce elongation of the stalk of Caulobacter crescents. In this work the contribution of stalks to nutrient uptake will be studied using two Gram negative bacteria, C. crescentus and Asticcacaulis biprosthecum. The comparative analysis between the mechanisms of nutrient uptake in these two bacterial species will help determine if the stalks arose by common descent or independently as consequence of living in similar nutrient-depleted environments. In this proposal, a multi-disciplinary approach is utilized to determine how nutrients are taken up by the stalk and transported to the cell body to be metabolized. Approaches used in this study will include fluorescence microscopy, microfluidics, proteomics, physiology, and mathematical modeling.
The specific aims of this proposal are to: 1). determine the rates of diffusion of nutrients from the stalk to the cell body, 2). determine the mechanism and capacity of nutrient uptake by stalks, and 3). determine the complement of stalk proteins. The results of the experiments outlined in this proposal will provide valuable information about the stalk, a morphological adaptation, which likely allows the stalked bacteria to persist in nutrient-limited environments. Cell shape changes in response to environmental cues are well documented in a number of bacterial systems, including pathogens. Enhancing our understanding of how bacterial cell shapes are maintained, function, and change will provide valuable information about the ability of bacteria to persist in unfavorable environments. This information can be used to design strategies to impede the persistence and proliferation of bacteria in specific environments.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32AI072992-03
Application #
7638536
Study Section
Special Emphasis Panel (ZRG1-F13-P (20))
Program Officer
Korpela, Jukka K
Project Start
2007-06-15
Project End
2010-06-14
Budget Start
2009-06-15
Budget End
2010-06-14
Support Year
3
Fiscal Year
2009
Total Cost
$51,710
Indirect Cost
Name
Indiana University Bloomington
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
006046700
City
Bloomington
State
IN
Country
United States
Zip Code
47401
Daniel, Jeremy J; Givan, Scott A; Brun, Yves V et al. (2015) Draft Genome Sequence of Prosthecomicrobium hirschii ATCC 27832T. Genome Announc 3:
Hoffman, Michelle D; Zucker, Lauren I; Brown, Pamela J B et al. (2015) Timescales and Frequencies of Reversible and Irreversible Adhesion Events of Single Bacterial Cells. Anal Chem 87:12032-9
Jiang, Chao; Brown, Pamela J B; Ducret, Adrien et al. (2014) Sequential evolution of bacterial morphology by co-option of a developmental regulator. Nature 506:489-93
Wan, Zhe; Brown, Pamela J B; Elliott, Ellen N et al. (2013) The adhesive and cohesive properties of a bacterial polysaccharide adhesin are modulated by a deacetylase. Mol Microbiol 88:486-500
Madren, Seth M; Hoffman, Michelle D; Brown, Pamela J B et al. (2012) Microfluidic device for automated synchronization of bacterial cells. Anal Chem 84:8571-8
Li, Guanglai; Brown, Pamela J B; Tang, Jay X et al. (2012) Surface contact stimulates the just-in-time deployment of bacterial adhesins. Mol Microbiol 83:41-51
Kuru, Erkin; Hughes, H Velocity; Brown, Pamela J et al. (2012) In?Situ probing of newly synthesized peptidoglycan in live bacteria with fluorescent D-amino acids. Angew Chem Int Ed Engl 51:12519-23
Brown, Pamela J B; de Pedro, Miguel A; Kysela, David T et al. (2012) Polar growth in the Alphaproteobacterial order Rhizobiales. Proc Natl Acad Sci U S A 109:1697-701
Brown, Pamela J B; Kysela, David T; Brun, Yves V (2011) Polarity and the diversity of growth mechanisms in bacteria. Semin Cell Dev Biol 22:790-8
Chertkov, Olga; Brown, Pamela J B; Kysela, David T et al. (2011) Complete genome sequence of Hirschia baltica type strain (IFAM 1418(T)). Stand Genomic Sci 5:287-97

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