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Ecology and physiological potential of tundra soil bacteria

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Title
Ecology and physiological potential of tundra soil bacteria
Name (type = personal)
NamePart (type = family)
Gadkari
NamePart (type = given)
Preshita
NamePart (type = date)
1990-
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Preshita Gadkari
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author
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Haggblom
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Max
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Max Haggblom
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Advisory Committee
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chair
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Barkay
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Tamar
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Tamar Barkay
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Advisory Committee
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internal member
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Kerkhof
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Lee
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Lee Kerkhof
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Advisory Committee
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Mannisto
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Minna
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Minna Mannisto
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Advisory Committee
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outside member
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Rutgers University
Role
RoleTerm (authority = RULIB)
degree grantor
Name (type = corporate)
NamePart
School of Graduate Studies
Role
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school
TypeOfResource
Text
Genre (authority = marcgt)
theses
OriginInfo
DateCreated (qualifier = exact)
2019
DateOther (qualifier = exact); (type = degree)
2019-01
CopyrightDate (encoding = w3cdtf)
2019
Place
PlaceTerm (type = code)
xx
Language
LanguageTerm (authority = ISO639-2b); (type = code)
eng
Abstract (type = abstract)
Arctic tundra soils cover a vast portion of the planet, store massive amounts of carbon, and harbor microbial life throughout all seasons. Bacteria in Arctic tundra soils impact global carbon cycling, and their capabilities are becoming more consequential with climate change. This research aimed to understand metabolic capabilities of tundra bacteria and identify metabolically-active bacteria in frozen tundra soil. The Arctic tundra site of Kilpisjärvi, Finland served as a model landscape to explore the ecology and physiological potential of bacteria using bacterial isolates and soil incubations.

The effect of thaw on tundra soil bacteria is starting to be better understood, but very little is known about the impact of subzero temperature changes, when the ground is frozen. Soil respiration continues in the winter, though at slower rates. Identifying cryo-active bacterial communities is important since soil respiration is largely determined by microbial C mineralization through decomposition of complex soil organic matter. Although previous studies have examined the microbiomes of frozen soils, most have failed to detect which members of the bacterial communities are metabolically active. This detection is important as cold temperatures preserve commonly measured biomolecules such as DNA, RNA, etc., and may provide misleading information. To ascertain metabolically-active bacteria, stable-isotope probing of tundra soil incubations with 13C-cellobiose at subzero temperatures of 0, -4, and -16°C was carried out, and numerous active bacterial phyla including the Ignavibacteria, Candidatus Saccharibacteria, Verrucomicrobia were detected. Temperature was shown to impact which members of the bacterial community assimilated cellobiose, even within subzero ranges. Phylogenies of members of cryo-active bacterial phyla were further explored, and added new insights to known physiological capabilities of these groups. Implications of different bacterial communities active within subzero temperatures may suggest that nutrient cycling may be impacted by temperature shifts within frozen soils.

Another gap in tundra bacteriology is understanding the physiological abilities of tundra soil isolates. Arctic tundra soil isolates such as Mucilaginibacter mallensis, along with other members of the Mucilaginibacter genus are hypothesized to play an important role in processing carbon, but their genomic capabilities remain unexplored. Genomic analysis revealed that M. mallensis strain MP1X4 was adapted to process complex carbon, and had an abundance of loci associated with polysaccharide utilization and Carbohydrate Active Enzymes compared to other members of the genus. Other Arctic tundra isolates such as the Acidobacteria were found to have unusual membrane-bound isoprenoid structures such as hopanoids and carotenoids. These carotenoids and hopanoids are hypothesized to aid maintaining membrane fluidity. Arctic Acidobacteria such as Granulicella mallensis MP5ACTX8, Granulicella tundricola MP5ACTX9, Terriglobus saanensis SP1PR4, and new isolates A2288, M8UP23, M8UP39, MP8S11, MP8S7, and MP8S9 had their genomes sequenced, from which isoprenoid pathways were investigated. From genomic analysis of these Acidobacteria, biosynthetic pathways of carotenoids, such as phytoene, zeta-carotene, neurosporene, lycopene, and hopanoids, such such as diploptene, adenosylhopane, ribosylhopane, bacteriohopanetetrol (BHT), BHT acetylglucosamine, BHT glucosamine, and BHT cyclitol ether, were detected for some species.

Investigation into the ecology and genomes of Arctic bacteria provided insights into the bacterial communities assimilating carbon in subzero temperatures, and the possible genomic adaptations that allow these bacteria to live in the Arctic tundra soils.
Subject (authority = RUETD)
Topic
Microbial Biology
Subject (authority = ETD-LCSH)
Topic
Tundra soils
Subject (authority = ETD-LCSH)
Topic
Bacteria -- Physiology
RelatedItem (type = host)
TitleInfo
Title
Rutgers University Electronic Theses and Dissertations
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ETD
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ETD_9420
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electronic resource
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application/pdf
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text/xml
Extent
1 online resource (139 pages : illustrations)
Note (type = degree)
Ph.D.
Note (type = bibliography)
Includes bibliographical references
Note (type = statement of responsibility)
by Preshita Gadkari
Subject (authority = lcsh/lcnaf)
Geographic
Kilpisjärvi (Finland and Sweden)
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TitleInfo
Title
School of Graduate Studies Electronic Theses and Dissertations
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rucore10001600001
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NjNbRU
Identifier (type = doi)
doi:10.7282/t3-7jmn-2697
Genre (authority = ExL-Esploro)
ETD doctoral
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The author owns the copyright to this work.
RightsHolder (type = personal)
Name
FamilyName
Gadkari
GivenName
Preshita
Role
Copyright Holder
RightsEvent
Type
Permission or license
DateTime (encoding = w3cdtf); (qualifier = exact); (point = start)
2018-12-12 08:29:08
AssociatedEntity
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Preshita Gadkari
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Affiliation
Rutgers University. School of Graduate Studies
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Author Agreement License
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I hereby grant to the Rutgers University Libraries and to my school the non-exclusive right to archive, reproduce and distribute my thesis or dissertation, in whole or in part, and/or my abstract, in whole or in part, in and from an electronic format, subject to the release date subsequently stipulated in this submittal form and approved by my school. I represent and stipulate that the thesis or dissertation and its abstract are my original work, that they do not infringe or violate any rights of others, and that I make these grants as the sole owner of the rights to my thesis or dissertation and its abstract. I represent that I have obtained written permissions, when necessary, from the owner(s) of each third party copyrighted matter to be included in my thesis or dissertation and will supply copies of such upon request by my school. I acknowledge that RU ETD and my school will not distribute my thesis or dissertation or its abstract if, in their reasonable judgment, they believe all such rights have not been secured. I acknowledge that I retain ownership rights to the copyright of my work. I also retain the right to use all or part of this thesis or dissertation in future works, such as articles or books.
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2019-01-31
DateTime (encoding = w3cdtf); (qualifier = exact); (point = end)
2020-01-31
Detail
Access to this PDF has been restricted at the author's request. It will be publicly available after January 31st, 2020.
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Copyright protected
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