Show simple item record

dc.contributor.authorNivens, David E.
dc.contributor.authorOhman, Dennis E.
dc.contributor.authorWilliams, Jessica
dc.contributor.authorFranklin, Michael J.
dc.identifier.citationNivens DE, Ohman DE, Williams J, Franklin MJ, "Role of alginate and alginate O-acetylation in the formation of Pseudomonas aeruginosa microcolonies and biofilms," J Bacteriol, 2001 183:1047-1057en_US
dc.description.abstractAttenuated total reflection/Fourier transform-infrared spectrometry (ATR/FT-IR) and scanning confocal laser microscopy (SCLM) were used to study the role of alginate and alginate structure in the attachment and growth of Pseudomonas aeruginosa on surfaces. Developing biofilms of the mucoid (alginate-producing) cystic fibrosis pulmonary isolate FRD1, as well as mucoid and nonmucoid mutant strains, were monitored by ATR/FT-IR for 44 and 88 h as IR absorbance bands in the region of 2,000 to 1,000 cm−1. All strains produced biofilms that absorbed IR radiation near 1,650 cm−1 (amide I), 1,550 cm−1 (amide II), 1,240 cm−1 (PO stretching, C—O—C stretching, and/or amide III vibrations), 1,100 to 1,000 cm−1(C—OH and P—O stretching) 1,450 cm−1, and 1,400 cm−1. The FRD1 biofilms produced spectra with an increase in relative absorbance at 1,060 cm−1 (C—OH stretching of alginate) and 1,250 cm−1 (C—O stretching of the O-acetyl group in alginate), as compared to biofilms of nonmucoid mutant strains. Dehydration of an 88-h FRD1 biofilm revealed other IR bands that were also found in the spectrum of purified FRD1 alginate. These results provide evidence that alginate was present within the FRD1 biofilms and at greater relative concentrations at depths exceeding 1 μm, the analysis range for the ATR/FT-IR technique. After 88 h, biofilms of the nonmucoid strains produced amide II absorbances that were six to eight times as intense as those of the mucoid FRD1 parent strain. However, the cell densities in biofilms were similar, suggesting that FRD1 formed biofilms with most cells at depths that exceeded the analysis range of the ATR/FT-IR technique. SCLM analysis confirmed this result, demonstrating that nonmucoid strains formed densely packed biofilms that were generally less than 6 μm in depth. In contrast, FRD1 produced microcolonies that were approximately 40 μm in depth. An algJ mutant strain that produced alginate lacking O-acetyl groups gave an amide II signal approximately fivefold weaker than that of FRD1 and produced small microcolonies. After 44 h, the algJ mutant switched to the nonmucoid phenotype and formed uniform biofilms, similar to biofilms produced by the nonmucoid strains. These results demonstrate that alginate, although not required for P. aeruginosa biofilm development, plays a role in the biofilm structure and may act as intercellular material, required for formation of thicker three-dimensional biofilms. The results also demonstrate the importance of alginate O acetylation in P. aeruginosabiofilm architecture.en_US
dc.titleRole of alginate and alginate O-acetylation in the formation of Pseudomonas aeruginosa microcolonies and biofilmsen_US
mus.citation.journaltitleJournal of Bacteriologyen_US
mus.identifier.categoryEngineering & Computer Scienceen_US
mus.relation.collegeCollege of Engineeringen_US
mus.relation.departmentCenter for Biofilm Engineering.en_US
mus.relation.departmentChemical & Biological Engineering.en_US
mus.relation.departmentChemical Engineering.en_US
mus.relation.universityMontana State University - Bozemanen_US
mus.relation.researchgroupCenter for Biofilm Engineering.en_US

Files in this item


This item appears in the following Collection(s)

Show simple item record

MSU uses DSpace software, copyright © 2002-2017  Duraspace. For library collections that are not accessible, we are committed to providing reasonable accommodations and timely access to users with disabilities. For assistance, please submit an accessibility request for library material.