Unique Cellular, Physiological, and Metabolic Adaptations to the Euendolithic Lifestyle in a Boring Cyanobacterium.

abstract: Euendolithic cyanobacteria have the remarkable ability to actively excavate and grow within certain minerals. Their activity leads to increased erosion of marine and terrestrial carbonates, negatively affecting coral reef and bivalve ecology. Despite their environmental relevance, the bori...

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Other Authors: Guida, Brandon Scott (Author)
Format: Doctoral Thesis
Language:English
Published: 2016
Subjects:
Online Access:http://hdl.handle.net/2286/R.I.38713
id ndltd-asu.edu-item-38713
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spelling ndltd-asu.edu-item-387132018-06-22T03:07:26Z Unique Cellular, Physiological, and Metabolic Adaptations to the Euendolithic Lifestyle in a Boring Cyanobacterium. abstract: Euendolithic cyanobacteria have the remarkable ability to actively excavate and grow within certain minerals. Their activity leads to increased erosion of marine and terrestrial carbonates, negatively affecting coral reef and bivalve ecology. Despite their environmental relevance, the boring mechanism has remained elusive and paradoxical, in that cyanobacteria alkalinize their surroundings, typically leading to carbonate precipitation, not dissolution. Thus, euendoliths must rely on unique adaptations to bore. Recent work using the filamentous model euendolith Mastigocoleus testarum strain BC008 indicated that excavation relied on transcellular calcium transport mediated by P-type ATPases, but the phenomenon remained unclear. Here I present evidence that excavation in M. testarum involves an unprecedented set of adaptations. Long-range calcium transport is achieved through the coordinated pumping of multiple cells, orchestrated by the localization of calcium ATPases in a repeating annular pattern, positioned at a single cell pole, adjacent to each cell septum along the filament. Additionally, specialized chlorotic cells that I named calcicytes, differentiate and accumulate calcium at concentrations more than 500 fold those of canonical cells, likely allowing for fast calcium flow at non-toxic concentrations through undifferentiated cells. I also show, using 13C stable isotope tracers and NanoSIMS imaging, that endolithic M. testarum derives most of its carbon from the mineral carbonates it dissolves, the first autotroph ever shown to fix mineral carbon, confirming the existence of a direct link between oxidized solid carbon pools and reduced organic pools in the biosphere. Finally, using genomic and transcriptomic approaches, I analyze gene expression searching for additional adaptations related to the endolithic lifestyle. A large and diverse set of genes (24% of 6917 genes) were significantly differentially regulated while boring, including several master regulators and genes expectedly needed under this condition (such as transport, nutrient scavenging, oxidative stress, and calcium-binding protein genes). However, I also discovered the up-regulation of several puzzling gene sets involved in alternative carbon fixation pathways, anaerobic metabolism, and some related to photosynthesis and respiration. This transcriptomic data provides us with several new, readily testable hypotheses regarding adaptations to the endolithic lifestyle. In all, my data clearly show that boring organisms show extraordinarily interesting adaptations. Dissertation/Thesis Guida, Brandon Scott (Author) Garcia-Pichel, Ferran (Advisor) Chandler, Douglas (Committee member) Bingham, Scott (Committee member) Roberson, Robert (Committee member) Arizona State University (Publisher) Molecular biology Microbiology Cellular biology benthic bioerosion cyanobacteria endolith intracellular calcium eng 222 pages Doctoral Dissertation Microbiology 2016 Doctoral Dissertation http://hdl.handle.net/2286/R.I.38713 http://rightsstatements.org/vocab/InC/1.0/ All Rights Reserved 2016
collection NDLTD
language English
format Doctoral Thesis
sources NDLTD
topic Molecular biology
Microbiology
Cellular biology
benthic
bioerosion
cyanobacteria
endolith
intracellular calcium
spellingShingle Molecular biology
Microbiology
Cellular biology
benthic
bioerosion
cyanobacteria
endolith
intracellular calcium
Unique Cellular, Physiological, and Metabolic Adaptations to the Euendolithic Lifestyle in a Boring Cyanobacterium.
description abstract: Euendolithic cyanobacteria have the remarkable ability to actively excavate and grow within certain minerals. Their activity leads to increased erosion of marine and terrestrial carbonates, negatively affecting coral reef and bivalve ecology. Despite their environmental relevance, the boring mechanism has remained elusive and paradoxical, in that cyanobacteria alkalinize their surroundings, typically leading to carbonate precipitation, not dissolution. Thus, euendoliths must rely on unique adaptations to bore. Recent work using the filamentous model euendolith Mastigocoleus testarum strain BC008 indicated that excavation relied on transcellular calcium transport mediated by P-type ATPases, but the phenomenon remained unclear. Here I present evidence that excavation in M. testarum involves an unprecedented set of adaptations. Long-range calcium transport is achieved through the coordinated pumping of multiple cells, orchestrated by the localization of calcium ATPases in a repeating annular pattern, positioned at a single cell pole, adjacent to each cell septum along the filament. Additionally, specialized chlorotic cells that I named calcicytes, differentiate and accumulate calcium at concentrations more than 500 fold those of canonical cells, likely allowing for fast calcium flow at non-toxic concentrations through undifferentiated cells. I also show, using 13C stable isotope tracers and NanoSIMS imaging, that endolithic M. testarum derives most of its carbon from the mineral carbonates it dissolves, the first autotroph ever shown to fix mineral carbon, confirming the existence of a direct link between oxidized solid carbon pools and reduced organic pools in the biosphere. Finally, using genomic and transcriptomic approaches, I analyze gene expression searching for additional adaptations related to the endolithic lifestyle. A large and diverse set of genes (24% of 6917 genes) were significantly differentially regulated while boring, including several master regulators and genes expectedly needed under this condition (such as transport, nutrient scavenging, oxidative stress, and calcium-binding protein genes). However, I also discovered the up-regulation of several puzzling gene sets involved in alternative carbon fixation pathways, anaerobic metabolism, and some related to photosynthesis and respiration. This transcriptomic data provides us with several new, readily testable hypotheses regarding adaptations to the endolithic lifestyle. In all, my data clearly show that boring organisms show extraordinarily interesting adaptations. === Dissertation/Thesis === Doctoral Dissertation Microbiology 2016
author2 Guida, Brandon Scott (Author)
author_facet Guida, Brandon Scott (Author)
title Unique Cellular, Physiological, and Metabolic Adaptations to the Euendolithic Lifestyle in a Boring Cyanobacterium.
title_short Unique Cellular, Physiological, and Metabolic Adaptations to the Euendolithic Lifestyle in a Boring Cyanobacterium.
title_full Unique Cellular, Physiological, and Metabolic Adaptations to the Euendolithic Lifestyle in a Boring Cyanobacterium.
title_fullStr Unique Cellular, Physiological, and Metabolic Adaptations to the Euendolithic Lifestyle in a Boring Cyanobacterium.
title_full_unstemmed Unique Cellular, Physiological, and Metabolic Adaptations to the Euendolithic Lifestyle in a Boring Cyanobacterium.
title_sort unique cellular, physiological, and metabolic adaptations to the euendolithic lifestyle in a boring cyanobacterium.
publishDate 2016
url http://hdl.handle.net/2286/R.I.38713
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