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pmid:30891015

Mixotrophic Growth Under Micro-Oxic Conditions in the Purple Sulfur Bacterium "Thiodictyon syntrophicum".

Samuel M Luedin · Nicola Storelli · Francesco Danza · Samuele Roman · Matthias Wittwer · Joël F Pothier · Mauro Tonolla

Frontiers in microbiology · 2019 doi:10.3389/fmicb.2019.00384

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Experiment

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Data

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title
Mixotrophic Growth Under Micro-Oxic Conditions in the Purple Sulfur Bacterium "Thiodictyon syntrophicum".
doi
10.3389/fmicb.2019.00384
pmid
30891015
authors array · 7 items
[0]
Samuel M Luedin
[1]
Nicola Storelli
[2]
Francesco Danza
[3]
Samuele Roman
[4]
Matthias Wittwer
[5]
Joël F Pothier
[6]
Mauro Tonolla
journal
Frontiers in microbiology
year
2019
abstract
The microbial ecosystem of the meromictic Lake Cadagno (Ticino, Swiss Alps) has been studied intensively in order to understand structure and functioning of the anoxygenic phototrophic sulfur bacteria community living in the chemocline. It has been found that the purple sulfur bacterium "Thiodictyon syntrophicum" strain Cad16T, belonging to the Chromatiaceae, fixes around 26% of all bulk inorganic carbon in the chemocline, both during day and night. With this study, we elucidated for the first time the mode of carbon fixation of str. Cad16T under micro-oxic conditions with a combination of long-term monitoring of key physicochemical parameters with CTD, 14C-incorporation experiments and quantitative proteomics using in-situ dialysis bag incubations of str. Cad16T cultures. Regular vertical CTD profiling during the study period in summer 2017 revealed that the chemocline sank from 12 to 14 m which was accompanied by a bloom of cyanobacteria and the subsequent oxygenation of the deeper water column. Sampling was performed both day and night. CO2 assimilation rates were higher during the light period compared to those in the dark, both in the chemocline population and in the incubated cultures. The relative change in the proteome between day and night (663 quantified proteins) comprised only 1% of all proteins encoded in str. Cad16T. Oxidative respiration pathways were upregulated at light, whereas stress-related mechanisms prevailed during the night. These results indicate that low light availability and the co-occurring oxygenation of the chemocline induced mixotrophic growth in str. Cad16T. Our study thereby helps to further understand the consequences micro-oxic conditions for phototrophic sulfur oxidizing bacteria. The complete proteome data have been deposited to the ProteomeXchange database with identifier PXD010641.
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Raw data was statistically analyzed using t-tests in Excel (Microsoft Office 2010, v-0.14.0.7168.5000).
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Genomic Data Availability The complete genome of str. Cad16T (Luedin et al., 2018a) is available under the GenBank assembly GCA_002813775.1. Proteomic Data Availability The complete proteomic data of str. Cad16T have been deposited to the ProteomeXchange Consortium (ProteomeXchange Datasets2) via the PRIDE partner repository (Vizcaíno et al., 2012) under the accession PXD010641 and project DOI 10.6019/PXD010641.
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sections[12] "Genomic Data Availability" paragraphs 1-2
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Genomic Data Availability The complete genome of str.
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Cad16T (Luedin et al., 2018a) is available under the GenBank assembly GCA_002813775.1.
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Proteomic Data Availability The complete proteomic data of str.
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Cad16T have been deposited to the ProteomeXchange Consortium (ProteomeXchange Datasets2) via the PRIDE partner repository (Vizcaíno et al., 2012) under the accession PXD010641 and project DOI 10.6019/PXD010641.
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Genomic Data Availability The complete genome of str. Cad16T (Luedin et al., 2018a) is available under the GenBank assembly GCA_002813775.1. Proteomic Data Availability The complete proteomic data of str. Cad16T have been deposited to the ProteomeXchange Consortium (ProteomeXchange Datasets2) via the PRIDE partner repository (Vizcaíno et al., 2012) under the accession PXD010641 and project DOI 10.6019/PXD010641.
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Genomic Data Availability The complete genome of str. Cad16T (Luedin et al., 2018a) is available under the GenBank assembly GCA_002813775.1. Proteomic Data Availability The complete proteomic data of str. Cad16T have been deposited to the ProteomeXchange Consortium (ProteomeXchange Datasets2) via the PRIDE partner repository (Vizcaíno et al., 2012) under the accession PXD010641 and project DOI 10.6019/PXD010641.
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Anoxygenic Photosynthesis and Dark Carbon Metabolism in the Purple Sulfur Bacterium “Thiodictyon syntrophicum“ nov. strain Cad16T
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Functional categories of “Thiodictyon syntrophicum” strain Cad16T proteins that were identified with LC-MS2.
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[11] array · 3 items
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List of “Thiodictyon syntrophicum” strain Cad16T proteins identified as more abundant in the light period.
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List of “Thiodictyon syntrophicum” strain Cad16T proteins identified as more abundant in the light period.
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3.83
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List of “Thyodictyon syntrophicum” strain Cad16T proteins identified as more abundant in the dark period.
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List of “Thyodictyon syntrophicum” strain Cad16T proteins identified as more abundant in the dark period.
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2.76
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[4]
6.66E-10
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5.26
[4]
9.24E-09
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3.81E-03
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2.65
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[4]
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[26] array · 5 items
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AUB82842.1
[1]
Dinitrogenase iron-molybdenum cofactor biosynthesis protein
[2]
S
[3]
3.30
[4]
3.81E-03
[27] array · 5 items
[0]
AUB83253.1
[1]
Nitrogen fixation protein
[2]
S
[3]
2.96
[4]
3.81E-03
[28] array · 5 items
[0]
AUB83860.1
[1]
Tellurite resistance protein TehB
[2]
S
[3]
2.76
[4]
1.23E-02
[29] array · 5 items
[0]
AUB83943.1
[1]
Short-chain dehydrogenase reductase SDR
[2]
S
[3]
2.91
[4]
4.18E-03
[30] array · 5 items
[0]
AUB84318.1
[1]
Transposase
[2]
S
[3]
2.99
[4]
3.81E-03
[31] array · 5 items
[0]
AUB84331.1
[1]
Dienelactone hydrolase
[2]
S
[3]
2.91
[4]
4.18E-03
[32] array · 5 items
[0]
AUB85354.1
[1]
Protein of unknown function (DUF2868)
[2]
S
[3]
3.78
[4]
2.26E-04
[33] array · 5 items
[0]
AUB82296.1
[1]
Ppx GppA phosphatase
[2]
T
[3]
2.79
[4]
1.23E-02
[34] array · 5 items
[0]
AUB82910.1
[1]
YciI-like protein
[2]
T
[3]
2.63
[4]
2.93E-02
[35] array · 5 items
[0]
AUB79943.1
[1]
General secretion pathway protein G
[2]
U
[3]
2.96
[4]
3.81E-03
[36] array · 5 items
[0]
AUB80110.1
[1]
Hypothetical protein
[2]
–
[3]
3.21
[4]
3.81E-03
[37] array · 5 items
[0]
AUB81753.1
[1]
ATPase
[2]
–
[3]
4.76
[4]
1.20E-06
[38] array · 5 items
[0]
AUB82624.1
[1]
Hypothetical protein
[2]
–
[3]
2.81
[4]
1.23E-02
[39] array · 5 items
[0]
AUB82926.1
[1]
Hypothetical protein
[2]
–
[3]
2.99
[4]
3.81E-03
locator
section[21]/table-wrap[2]#T3
[5] object · 16 fields
id
asset:table:pmid:30891015:4
role
table
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jats-table
media_type
application/vnd.jats.table+json
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null
sha256
sha256:9d9944580ff0581a49d139f7cb719b905533bf248e01e56ede4a1f7996f00c5b
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read_table
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note
Absolute carbon uptake rates of the microbial community in the Lake Cadagno chemocline.
structure object · 5 fields
pmcid
PMC6413534
section_index
22
section_title
Discussion
row_count
9
column_count
6
table object · 8 fields
label
Table 4
caption
Absolute carbon uptake rates of the microbial community in the Lake Cadagno chemocline.
rows array · 9 items
[0] array · 4 items
[0]
[1]
Conditions
[2]
[3]
[1] array · 5 items
[0]
[1]
Light
[2]
Dark
[3]
[4]
[2] array · 6 items
[0]
Photosynthesis
[1]
Oxygenic
[2]
Anoxygenic
[3]
[4]
Depth [m]
[5]
References
[3] array · 6 items
[0]
Carbon Uptake Rates [nM h−1]
[1]
3,825
[2]
4,175
[3]
7,608
[4]
11.5
[5]
Camacho et al., 2001
[4] array · 5 items
[0]
[1]
1,200
[2]
–
[3]
11.5
[4]
Musat et al., 2008
[5] array · 5 items
[0]
[1]
85
[2]
25
[3]
12.5
[4]
Halm et al., 2009
[6] array · 5 items
[0]
[1]
6,187
[2]
4,812
[3]
12.0
[4]
Storelli et al., 2013
[7] array · 5 items
[0]
[1]
987
[2]
–
[3]
11.4
[4]
Berg et al., 2016
[8] array · 5 items
[0]
[1]
757
[2]
587
[3]
14.0
[4]
This study
locator
section[22]/table-wrap[1]#T4
gaps array · 2 items
[0]
asset:data:geo:PXD010641 not downloaded
[1]
asset:data:geo:PXD010641 licence not read
analysis object · 4 fields
state
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methods array · 1 item
[0] object · 10 fields
id
method-1
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null
specific
null
label
t-test
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missing_operations array · 0 items
parameters object · 0 fields
data_shapes array · 0 items
evidence object · 3 fields
score
1
band
verbatim
quote
Raw data was statistically analyzed using t-tests in Excel (Microsoft Office 2010, v-0.14.0.7168.5000).
targets array · 0 items
gaps array · 1 item
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method.reader_named_unmapped
capability object · 3 fields
state
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capability_id
capability:computational_analysis
label
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assay_families array · 9 items
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meta_analysis
[1]
machine_learning
[2]
survival_analysis
[3]
statistical_regression
[4]
pca
[5]
molecular_docking
[6]
network_analysis
[7]
differential_expression
[8]
gwas
candidate
Automated Assays Laravel application and simulated adapters
gaps array · 0 items
readiness object · 8 fields
state
blocked
tier
R4
blocking_axis
method
blocked_on
method:not_determinable
axes object · 3 fields
method object · 5 fields
tier
R4
expressible
false
required_operations array · 0 items
missing_operations array · 0 items
basis
The reader quoted the method the paper names (t-test), but the corpus's method extractor could not map it onto a DSL operation, so the method is published but not expressible.
capability object · 4 fields
tier
R1
capability_id
capability:computational_analysis
availability_state
owned
basis
The computational analysis is owned. The physical bench the paper used is not, so a physical validation cannot be run here.
data object · 6 fields
tier
R1
reachable
true
accessions array · 1 item
[0]
PXD010641
resolved_accessions array · 1 item
[0]
PXD010641
statements array · 1 item
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Genomic Data Availability The complete genome of str. Cad16T (Luedin et al., 2018a) is available under the GenBank assembly GCA_002813775.1. Proteomic Data Availability The complete proteomic data of str. Cad16T have been deposited to the ProteomeXchange Consortium (ProteomeXchange Datasets2) via the PRIDE partner repository (Vizcaíno et al., 2012) under the accession PXD010641 and project DOI 10.6019/PXD010641.
basis
The paper names PXD010641 in ProteomeXchange Consortium via the PRIDE partner repository and the accession resolves in the repository. No dataset was downloaded and no licence was read.
can_run object · 3 fields
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source:pmid:30891015
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asset:table:pmid:30891015:1
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asset:table:pmid:30891015:2
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asset:table:pmid:30891015:3
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asset:table:pmid:30891015:4
steps array · 1 item
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run_analysis
must_build object · 5 fields
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data_gaps array · 1 item
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data:geo:PXD010641
gaps array · 1 item
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method:not_determinable
review object · 5 fields
state
partial
machine_critique object · 5 fields
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extraction_review
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MiniMax-M3.1-Flash
provider
minimax
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minimax
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independence
single_reader
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method
verbatim
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completion_tokens
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id
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MiniMax-M3.1-Flash
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minimax
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review.independent_reader
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review.machine_critique
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review.human_critique
execution object · 5 fields
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not_run
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execution.not_run
provenance object · 7 fields
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pmid:30891015
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paper
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pmid:30891015
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source:pmid:30891015
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manuscript
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PMID 30891015 full text
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data:geo:PXD010641
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dataset
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activity-reading-sci-2026-11-01
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pmid:30891015
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id
source:pmid:30891015
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data:geo:PXD010641
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agent:corpus-assay-engine
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agent:minimax-reader
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activity-resolve-PXD010641
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data:geo:PXD010641
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agent:corpus-assay-engine
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Complete file
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It has been found that the purple sulfur bacterium \"Thiodictyon syntrophicum\" strain Cad16T, belonging to the Chromatiaceae, fixes around 26% of all bulk inorganic carbon in the chemocline, both during day and night. With this study, we elucidated for the first time the mode of carbon fixation of str. Cad16T under micro-oxic conditions with a combination of long-term monitoring of key physicochemical parameters with CTD, 14C-incorporation experiments and quantitative proteomics using in-situ dialysis bag incubations of str. Cad16T cultures. Regular vertical CTD profiling during the study period in summer 2017 revealed that the chemocline sank from 12 to 14 m which was accompanied by a bloom of cyanobacteria and the subsequent oxygenation of the deeper water column. Sampling was performed both day and night. CO2 assimilation rates were higher during the light period compared to those in the dark, both in the chemocline population and in the incubated cultures. The relative change in the proteome between day and night (663 quantified proteins) comprised only 1% of all proteins encoded in str. Cad16T. Oxidative respiration pathways were upregulated at light, whereas stress-related mechanisms prevailed during the night. These results indicate that low light availability and the co-occurring oxygenation of the chemocline induced mixotrophic growth in str. Cad16T. Our study thereby helps to further understand the consequences micro-oxic conditions for phototrophic sulfur oxidizing bacteria. 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“Thyodictyon syntrophicum” strain Cad16T proteins identified as more abundant in the dark period.", "structure": {"pmcid": "PMC6413534", "section_index": 21, "section_title": "Proteins Differentially Expressed", "row_count": 40, "column_count": 5}, "table": {"label": "Table 3", "caption": "List of “Thyodictyon syntrophicum” strain Cad16T proteins identified as more abundant in the dark period.", "rows": [["Accession", "Name", "COG category", "cat score", "lfdr"], ["AUB80187.1", "Isocitrate dehydrogenase (NADP)", "C", "2.94", "3.81E-03"], ["AUB81294.1", "Oxidoreductase", "C", "3.54", "2.26E-04"], ["AUB82371.1", "Adenylylsulfate reductase alpha subunit", "C", "3.03", "3.81E-03"], ["AUB83156.1", "NADH dehydrogenase NAD(P)H nitroreductase", "C", "3.03", "3.81E-03"], ["AUB84003.1", "Rubrerythrin", "C", "2.54", "4.44E-02"], ["AUB80125.1", "Cell division protein FtsZ", "D", "2.67", "2.93E-02"], ["AUB79575.1", "Extracellular solute-binding protein, family 3", "E", "2.62", "4.44E-02"], ["AUB81750.1", "Decarboxylase", "E", "2.63", "2.93E-02"], ["AUB83785.1", "4-hydroxy-tetrahydrodipicolinate synthase", "E", "2.94", "4.18E-03"], ["AUB84954.1", "acetolactate synthase", "E", "2.76", "1.95E-02"], ["AUB84325.1", "Proline iminopeptidase", "E", "2.91", "4.18E-03"], ["AUB82337.1", "Adenylosuccinate synthase", "F", "2.54", "4.44E-02"], ["AUB79762.1", "Ubiquinone biosynthesis regulatory protein kinase UbiB", "H", "2.86", "1.23E-02"], ["AUB80927.1", "uBA THIF-type NAD FAD binding", "H", "2.64", "2.93E-02"], ["AUB83525.1", "Synthase", "I", "5.36", "6.66E-10"], ["AUB81024.1", "Lysyl-tRNA synthetase", "J", "3.31", "1.29E-03"], ["AUB79657.1", "OmpA MotB", "M", "5.26", "9.24E-09"], ["AUB80121.1", "Cell wall formation (By similarity)", "M", "3.04", "3.81E-03"], ["AUB83127.1", "Choloylglycine hydrolase", "M", "2.98", "3.81E-03"], ["AUB83783.1", "Conserved repeat domain protein", "M", "2.58", "4.44E-02"], ["AUB83066.1", "Twitching motility protein", "N, U", "3.14", "3.81E-03"], ["AUB79946.1", "Heat-shock protein", "O", "2.65", "2.93E-02"], ["AUB82608.1", "Endopeptidase La", "O", "5.02", "1.01E-07"], ["AUB85620.1", "DnaK-related protein", "O", "2.78", "1.23E-02"], ["AUB81090.1", "Protein of unknown function (DUF971)", "S", "3.55", "2.26E-04"], ["AUB82842.1", "Dinitrogenase iron-molybdenum cofactor biosynthesis protein", "S", "3.30", "3.81E-03"], ["AUB83253.1", "Nitrogen fixation protein", "S", "2.96", "3.81E-03"], ["AUB83860.1", "Tellurite resistance protein TehB", "S", "2.76", "1.23E-02"], ["AUB83943.1", "Short-chain dehydrogenase reductase SDR", "S", "2.91", "4.18E-03"], ["AUB84318.1", "Transposase", "S", "2.99", "3.81E-03"], ["AUB84331.1", "Dienelactone hydrolase", "S", "2.91", "4.18E-03"], ["AUB85354.1", "Protein of unknown function (DUF2868)", "S", "3.78", "2.26E-04"], ["AUB82296.1", "Ppx GppA phosphatase", "T", "2.79", "1.23E-02"], ["AUB82910.1", "YciI-like protein", "T", "2.63", "2.93E-02"], ["AUB79943.1", "General secretion pathway protein G", "U", 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