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A Study on Microbial Ecology in Permanently Ice-covered Lakes of McMurdo Dry Valleys, Antarctica

DC Field Value Language
dc.contributor.advisor김상종-
dc.contributor.author권미예-
dc.date.accessioned2017-10-27T17:11:52Z-
dc.date.available2017-10-27T17:11:52Z-
dc.date.issued2017-08-
dc.identifier.other000000144985-
dc.identifier.urihttps://hdl.handle.net/10371/137141-
dc.description학위논문 (박사)-- 서울대학교 대학원 자연과학대학 생명과학부, 2017. 8. 김상종.-
dc.description.abstractAntarctica has been considered as pristine and harsh environment in respect to microbes because of the extreme conditions. Perennially ice-covered lakes (Lake Fryxell, Lake Miers, and Lake Bonney) in the McMurdo Dry Valleys, Antarctica, are chemically stratified with depth and have distinct biological gradients. Despite of long-term research on these unique environments, the information on the structure of the microbial communities in the water columns of these lakes are scarce.
In this study, bacterial diversity in the ice-covered lakes in Antarctica was examined by 16S rRNA gene-based pyrosequencing. Distinct communities were present in each lake, reflecting the unique biogeochemical characteristics of these environments. Further, certain bacterial lineages were exclusively confined to specific depths within each lake. For example, candidate division WM88 occurred solely at a depth of 15 m in Lake Fryxell, whereas unknown lineages of Chlorobi were found only at a depth of 18 m in Lake Miers, and two distinct classes of Firmicutes inhabited East and West Lobe Bonney at depth of 30 m. Redundancy analysis revealed that community variation of bacterioplankton could be explained by the distinct conditions of each lake and depth
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dc.description.abstractin particular, assemblages from layers beneath the chemocline had biogeochemical associations that differed from those in the upper layers.
Despite of the fact that sulfate reduction has been actively detected, little is known about diversity of sulfate reducing bacteria in Lake Fryxell. Less than 1% of total bacteria are known to be culturable. By application of culture-independent approach such as metagenomics, not only full extent of bacterial diversity but also their ecological function could be obtained. Three draft genomes were recovered from metagenome data as sulfate reduction-related bacteria, two belonging to Deltaproteobacteria and one belonging to candidate division WM88. Deltaproteobacteria was a key player for sulfate reduction in Lake Fryxell whereas candidate division WM88 was indirectly related to the reaction of sulfate reduction. Other metabolic pathways were also investigated, and it was revealed that they were versatile in acquisition and usage of various carbon sources and energy conservation.
Another aspect of sulfate reducing bacteria in the bottom of Lake Fryxell was observed based on microcosm study as a culture-dependent approach. Through performing microcosm study using the lake water as a medium, previously uncultivated sulfate reducing bacteria were expected to be recovered from Lake Fryxell. From the microcosm culture, the genus Desulfosporosinus belonging to the phylum Firmicutes was surprisingly enriched in large proportion under specific conditions with low concentration of carbon source and sulfate. This genus has gained attention for the ability of sulfate reduction with high efficiency albeit low abundance in natural environments, which is known as rare biosphere.
The findings of patterns of bacterial community composition and their ecological functions, including sulfate reduction, may represent adaptation of bacteria to the extreme and unique biogeochemical gradients of ice-covered lakes in the McMurdo Dry Valleys. Also, novel results may provide further insights into the ecology and evolution of bacteria inhabiting the ice-covered lakes of Antarctica.
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dc.description.tableofcontentsCHAPTER 1. General introduction: Bacterial diversity and geochemistry in the ice-covered lakes, Antarctica 1
1.1 General information of McMurdo Dry Valleys, Antarctica 3
1.1.1. Antarctica and McMurdo Dry Valleys 3
1.1.2. Ice-covered lakes in McMurdo Dry Valleys 5
1.2. Microbial diversity and their pattern in the ice-covered lakes 9
1.2.1. Bacterial diversity and community structure in the ice-covered lakes 9
1.2.2. Diversity of sulfate-reducing bacteria in the ice-covered lake Fryxell 12
1.3. Moleculartechnologies formicrobial ecology 14
1.3.1. Molecular biological tools 4
1.3.2. High-throughput deep sequencing 15
1.4. Objectives of this study 16
CHAPTER 2.Bacterial community structure in permanently ice-covered lakes of McMurdo Dry Valleys, Antarctica 23
2.1. Introduction 25
2.2. Materials and Methods 27
2.2.1. Site description and sample collection 27
2.2.2. Chemical analyses and primary production measurements 28
2.2.3. Pyrosequencing and data analyses 29
2.2.4. Quantitative PCR 31
2.2.5. 16S rRNA gene cloning, sequencing and phylogenetic analysis 32
2.2.6. Statistical analyses 33
2.3. Results 35
2.3.1. Biogeochemical characteristics in five lakes of McMurdo dry valleys 35
2.3.2. Distribution and relative abundance of bacterial biomass 35
2.3.3. Distribution of bacterial phyla among lakes and depths 36
2.3.4. Bacterial differentiation between lakes and their relationship with physicochemical properties 39
2.3.5. Shared OTUsbetween lakes 41
2.4.Discussion 42
CHAPTER 3. Culture-independent approach:Insights into ecological function of sulfate-reducing bacteria using metagenomic analysis in ice-covered Lake Fryxell 69
3.1. Introduction 71
3.2. Materials and methods 74
3.2.1. Sample collection and DNA extraction 74
3.2.2. Metagenome shotgun sequencing, read trimming, de novoassembly and data binning 74
3.2.3. Community profiling with 16S rRNA gene and genome analysis. 75
3.2.4. Phylogenetic tree construction 76
3.3. Results 77
3.3.1. Bacterial community profiling using 16SrRNA gene 77
3.3.2. Comparison of metabolic pathway module between two size-fraction samples 77
3.3.3. Draft genomes and metabolic characterization for sulfate reducing bacteria 78
3.3.4. Phylogenetic positions of four draft genomes 81
3.4. Discussion 81
CHAPTER 4. Culture-dependent approach:culture strategies for sulfate reducing bacteria in ice-covered Lake Fryxell 105
4.1. Introduction 107
4.2. Materials and Methods 109
4.2.1. Sample collection and microcosm setup 109
4.2.2. Analytical methods 10
4.2.3. Serial transfers 111
4.2.4.Genomic DNA extraction 111
4.2.5. PCR amplification, cloning and sequencing 112
4.2.6. Quantitative real-time PCR 113
4.2.7. 16S rRNA gene amplicon sequencing, community and phylogeny analysis 114
4.3. Results 115
4.3.1. Evidence of sulfate reduction in microcosm 115
4.3.2. Shifts in bacterial community and identification of dominant populations during the anaerobic incubation 115
4.3.3. Quantification of bacteria and two targeted populations in FRX and microcosm samples 117
4.3.4. Phylogeny diversity of 16S rRNA gene and DsrAB gene in Desulfosporosinus 118
4.4. Discussion 118
CHAPTER 5. General conclusions 133
REFERENCES 139
국문초록(Abstract in Korean) 169
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dc.formatapplication/pdf-
dc.format.extent6038070 bytes-
dc.format.mediumapplication/pdf-
dc.language.isoen-
dc.publisher서울대학교 대학원-
dc.subjectbacterial diversity-
dc.subjectniche-specialization-
dc.subjectsulfate-reducing bacteria-
dc.subjectpyrosequecning-
dc.subjectmetagenome-
dc.subjectmicrocosm-
dc.subjectFryxell-
dc.subjectIce-covered lakes-
dc.subjectAntarctica-
dc.subject.ddc570-
dc.titleA Study on Microbial Ecology in Permanently Ice-covered Lakes of McMurdo Dry Valleys, Antarctica-
dc.typeThesis-
dc.description.degreeDoctor-
dc.contributor.affiliation자연과학대학 생명과학부-
dc.date.awarded2017-08-
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