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1.
Microb Ecol ; 78(1): 33-41, 2019 Jul.
Article in English | MEDLINE | ID: mdl-30267129

ABSTRACT

How ecological diversity is maintained and distributed within populations is a longstanding question in microbial ecology. In the thermophilic cyanobacterium Synechococcus B', high observed levels of recombination are predicted to maintain ecological variation despite the simultaneous action of diverse selective pressures on different regions of the genome. To investigate ecological diversity in these bacteria, we directly isolated laboratory strains of Synechococcus B' from samples collected along the thermal gradients of two geothermal environments in Yellowstone National Park. Extensive recombination was evident for a multi-locus sequence data set, and, consequently, our sample did not exhibit the sequence clustering expected for distinct ecotypes evolving by periodic clonal selection. Evidence for local selective sweeps at specific loci suggests that sweeps may be common but that recombination is effective for maintaining diversity of unlinked genomic regions. Thermal performance for strain growth was positively associated with the temperature of the environment, indicating that Synechococcus B' populations consist of locally adapted ecological specialists that occupy specific thermal niches. Because this ecological differentiation is observed despite the absence of dispersal barriers among sites, we conclude that these bacteria may freely exchange much of the genome but that barriers to gene flow exist for loci under direct temperature selection.


Subject(s)
Gene Flow , Hot Springs/microbiology , Synechococcus/genetics , Ecology , Ecosystem , Genomics , Hot Springs/chemistry , Hot Temperature , Phylogeny , Recombination, Genetic , Synechococcus/chemistry , Synechococcus/growth & development , Synechococcus/isolation & purification
2.
Mol Biol Evol ; 30(4): 752-60, 2013 Apr.
Article in English | MEDLINE | ID: mdl-23292343

ABSTRACT

A long-standing question in evolutionary biology is how organisms adapt to novel environments. In North American hot springs, diversification of a clade of the cyanobacterium Synechococcus into hotter environments has resulted in the unique innovation of a light-driven ecosystem at temperatures up to 74°C, and temperature adaptation of photosynthetic carbon fixation with the Calvin cycle contributed to this process. Here, we investigated the evolution of thermostability of the Calvin cycle enzyme ribulose-1, 5-bisphosphate carboxylase/oxygenase (RuBisCO) during Synechococcus divergence. Circular dichroism thermal scans revealed that the RuBisCO of the most thermotolerant Synechococcus lineage is more stable than those of other lineages or of resurrected ancestral enzymes. Using site-directed mutagenesis, we next identified four amino acid substitutions that together increased stability and activity of this enzyme at higher temperatures. These are clustered near critical subunit interfaces distant from the active site. Each of the four amino acids is also observed in a less thermostable Synechococcus RuBisCO, and the impact on stability of three of these appears to be epistatic. Recombination analyses that allow for recurrent mutation as well as patterns of synonymous variation surrounding these sites suggest that the evolution of a more thermostable RuBisCO may have involved homologous recombination. Our results provide insights on the molecular evolutionary processes that shape niche differentiation and ecosystem function.


Subject(s)
Bacterial Proteins/chemistry , Ribulose-Bisphosphate Carboxylase/chemistry , Synechococcus/enzymology , Adaptation, Biological/genetics , Amino Acid Substitution , Bacterial Proteins/genetics , Catalytic Domain , Circular Dichroism , Enzyme Stability , Evolution, Molecular , Hot Temperature , Hydrogen Bonding , Models, Molecular , Molecular Sequence Data , Mutagenesis, Site-Directed , Photosynthesis , Phylogeny , Protein Interaction Domains and Motifs , Protein Structure, Quaternary , Protein Unfolding , Ribulose-Bisphosphate Carboxylase/genetics , Transition Temperature
3.
Appl Environ Microbiol ; 75(3): 729-34, 2009 Feb.
Article in English | MEDLINE | ID: mdl-19047382

ABSTRACT

Laboratory evolution experiments suggest the potential for microbial populations to contribute significant ecological variation to ecosystems, yet the functional importance of genetic diversity within natural populations of microorganisms is largely unknown. Here, we investigated the distribution of genetic and phenotypic variation for a population of the cyanobacterium Mastigocladus laminosus distributed along the temperature gradient of White Creek, Yellowstone NP. A total of 153 laboratory strains were directly isolated from five sites with mean annual temperatures ranging between 39 and 54 degrees C. Genetic characterization at four nitrogen metabolism genes identified 15 closely related lineages in the population sample. These lineages were distributed nonrandomly along White Creek, but the observed geographic structure could not be explained by limited dispersal capabilities. Temperature performance experiments with six M. laminosus lineages that maximized their respective relative abundances at different positions along the gradient provided evidence for niche differentiation within the population. Niche differentiation included a tradeoff in performance at high and low temperatures, respectively. The physiological variation of these lineages in laboratory culture was generally well matched to the prevailing temperature conditions experienced by these organisms in situ. These results suggest that sympatric diversification along an ecological selection gradient can be a potent source of evolutionary innovation in microbial populations.


Subject(s)
Cyanobacteria/classification , Cyanobacteria/isolation & purification , Genetic Variation , Water Microbiology , Bacterial Proteins/genetics , Cluster Analysis , Cyanobacteria/genetics , DNA, Bacterial/chemistry , DNA, Bacterial/genetics , Ecosystem , Metabolic Networks and Pathways/genetics , Molecular Sequence Data , Phylogeny , Sequence Analysis, DNA , Temperature
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