de.pangaea.dataset937561 und dataset PANGAEA
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https://www.pangaea.de/ information pointOfContact 2026-07-10T14:49:27Z https://doi.pangaea.de/10.1594/PANGAEA.937561 <gco:CharacterString>Influence of flanking genes on Gammaproteobacterial form I and II RubisCO functioning</gco:CharacterString> 2021-10-26T12:50:23 publication https://doi.org/10.1594/PANGAEA.937561 Böhnke-Brandt, Stefanie
sboehnke-brandt@geomar.de
https://orcid.org/0000-0002-3431-5452 information author Perner, Mirjam
mperner@geomar.de
https://orcid.org/0000-0003-1223-9310 information author PANGAEA
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https://www.pangaea.de/ information publisher tableDigital Since the majority of all microorganisms are currently not culturable, we used a metagenomic approach to identify genes and enzymes associated with RubisCO expression. The investigated metagenomic DNA fragment originates from the deep-sea hydrothermal vent field Nibelungen at 8°18'S along the Mid-Atlantic Ridge. It is 13,023 bp and resembles genes from Thiomicrospira crunogena. The fragment encodes nine open reading frames (ORFs) which include two types of RubisCO, form I (CbbL/S) and form II (CbbM), two LysR transcriptional regulators (LysR1 and LysR2), two von Willebrand factor type A (CbbO-m and CbbO-1), and two AAA+ ATPases (CbbQ-m and CbbQ-1), expected to function as RubisCO activating enzymes. To date, only one study has ever investigated regulatory mechanisms in metagenome-derived RubisCO gene clusters (Böhnke and Perner 2015). Here, total RubisCO activity was significantly influenced when cbbL and cbbM neighboring genes were knocked out (Böhnke and Perner 2015), but it remained unclear which of the two RubisCOs was primarily affected by these mutations. Our study suggests that CbbQ-m and CbbO-m activate CbbL and that LysR1 and LysR2 proteins promote CbbQ-m/CbbO-m expression. CbbO-1 seems to activate CbbM and CbbM itself appears to contribute to intensifying LysR's binding ability and thus its own transcriptional regulation. CbbM furthermore appears to impair cbbL expression. completed Böhnke-Brandt, Stefanie
sboehnke-brandt@geomar.de
https://orcid.org/0000-0002-3431-5452 information principalInvestigator autotrophic CO2 fixation Calvin-Benson-Bassham (CBB) cycle CbbO CbbQ heterologous gene expression LysR non-native system RubisCO gene regulation theme <gco:CharacterString>PANGAEA Keyword List</gco:CharacterString> 1995-01-01 creation PANGAEA
info@pangaea.de
https://www.pangaea.de/ information pointOfContact DERIDGE From Mantle to Ocean: Energy-, Material- and Life-cycles at Spreading Axes RuBisCO Linkage between the distribution and biochemical properties of RuBisCO and CODH enzymes and abiotic properties in thermally and chemically distinct deep-sea hydrothermal vent systems theme <gco:CharacterString>PANGAEA Project List</gco:CharacterString> 1995-01-01 creation PANGAEA
info@pangaea.de
https://www.pangaea.de/ information pointOfContact copyright copyright CC-BY-4.0: Creative Commons Attribution 4.0 International textTable und geoscientificInformation -13.508833333333 -13.508833333333 -8.2971666666667 -8.2971666666667 2009-04-27T10:01:00 2009-04-27T10:01:00 Drachenschlund (Nibelungen hydrothermal vent field), sample type: fluid sample cruise. Fluid sample was collected within the DFG-SPP 1144 priority program “From Mantle to Ocean: Energy-, Material-, and Life-cycles at Spreading Axes" Work was granded by the Graduate School for C1-Chemistry in Resource and Energy Management and the DFG (Project PE1549/5 1 "Linkage between the distribution and biochemical properties of RubisCO and CODH enzymes and abiotic properties in thermally and chemically distinct deep-sea hydrothermal vent systems"). Crude extracts used for activity measurements were prepared after autoindiction. All fosmid clones were constructed with pCC1FOS vector and Epi300 as a host. The activity measurements were performed at 25°C in buffer A [100 mM Tris HCl (pH 7.8), 10 mM MgCl2, 1 mM EDTA, 25 mM NaHCO3, and 1 mM DTT] with 0.2 mg unpurified, total protein, and 5 mM ribulose 1.5 bisphosphate (Rubp), whereby Rubp addition is the initiation step. Quantification of RuPB and 3-PGA was done using High Pressure Liquid Chromatography (HPLC) (LaChrom Elite® system, Hitachi) with a Lichrospher® 100 RP 18e column (VWR International GmbH, Darmstadt, Germany), detection at 200 nm, acetonitrile as an eluent, and a flow of 0.6 ml per minute. Identification thematicClassification fosmid clone designation Insert size physicalMeasurement Sanger Sequencing modified after Sanger et al. (1977); PacBio Sequencing according to Rhoads and Au (2015) bp bp Gene name thematicClassification Sequence editing, BioEdit; inserted gene 1 Gene name thematicClassification Sequence editing, BioEdit; inserted gene 2 Insertion position physicalMeasurement gene 1; insertion position in non-coding region (ncr) is given in nucleotides aa aa Total length of inserted gene physicalMeasurement gene 1; insertion position in non-coding region (ncr) is given in nucleotides aa aa Insertion position physicalMeasurement gene 2; insertion position in non-coding region (ncr) is given in nucleotides aa aa Total length of inserted gene physicalMeasurement gene 2; insertion position in non-coding region (ncr) is given in nucleotides aa aa Specific ribulose-1,5-bisphosphate carboxylase/oxygenase activity physicalMeasurement High Performance Liquid Chromatography (HPLC) nmol/mg/min nmol/mg/min Specific ribulose-1,5-bisphosphate carboxylase/oxygenase activity, standard deviation physicalMeasurement Gaussian propagation of error ± ± text/tab-separated-values unknown https://doi.pangaea.de/10.1594/PANGAEA.937561?format=textfile download dataset The data set was checked for completeness, correctness, and consistency of metainformation. Validity of used methods was checked and - if applicable - precision and range of data. EVENT LABEL: M78/2_314 * LATITUDE: -8.297167 * LONGITUDE: -13.508833 * DATE/TIME: 2009-04-27T10:01:00 * ELEVATION: -2886.0 m * CAMPAIGN: M78/2 * BASIS: Meteor (1986) * METHOD/DEVICE: Remote operated vehicle 2009-04-27T10:01:00 Supplement to <gco:CharacterString>Unraveling RubisCO Form I and Form II Regulation in an Uncultured Organism from a Deep-Sea Hydrothermal Vent via Metagenomic and Mutagenesis Studies</gco:CharacterString> 2017-01-01 publication https://doi.org/10.3389/fmicb.2017.01303 Böhnke, Stefanie
sboehnke-brandt@geomar.de
https://orcid.org/0000-0002-3431-5452 information author Perner, Mirjam
mperner@geomar.de
https://orcid.org/0000-0003-1223-9310 information author documentDigital Frontiers in Microbiology 8