Summary of Study ST002511

This data is available at the NIH Common Fund's National Metabolomics Data Repository (NMDR) website, the Metabolomics Workbench, https://www.metabolomicsworkbench.org, where it has been assigned Project ID PR001621. The data can be accessed directly via it's Project DOI: 10.21228/M85M6X This work is supported by NIH grant, U2C- DK119886.

See: https://www.metabolomicsworkbench.org/about/howtocite.php

This study contains a large results data set and is not available in the mwTab file. It is only available for download via FTP as data file(s) here.

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Study IDST002511
Study TitleEnhanced niche colonization and competition during bacterial adaptation to a fungus
Study TypeFungal / bacterial interaction
Study SummaryEnhanced niche 1 colonization and competition during bacterial adaptation to a fungus
Institute
Netherlands Institute of Ecology
DepartmentMicrobial Ecology
Last NameTyc
First NameOlaf
AddressDroevendaalsesteeg 10, 6708 PB Wageningen, The Netherlands
EmailOlaf.Tyc@kgu.de
Phone+496963018046
Submit Date2023-03-16
Raw Data AvailableYes
Raw Data File Type(s)mzML
Analysis Type DetailGC-MS
Release Date2023-04-04
Release Version1
Olaf Tyc Olaf Tyc
https://dx.doi.org/10.21228/M85M6X
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Collection:

Collection ID:CO002604
Collection Summary:For analysis and trapping of volatile organic compounds two-compartment glass Petri-dishes (Garbeva et al., 2014) containing 1% LB-A (Carl-Roth LB- Agar) were applied. The fungus Aspergillus niger was inoculated 24 hours before addition of the bacterial strain on the left side of the two compartment glass petri-dish and incubated overnight at 28 °C. The bacterial strain Bacillus subtilis 3610 was incubated overnight at 28 °C in LB- liquid medium (Carl-Roth LB- Medium). After overnight _incubation a volume of 2 µl of the grown Bacillus subtilis 3610 culture was spotted on the opposite side of the Aspergillus niger culture. The glass Petri-dishes were kept open for 25 min. for drying of the droplets. After the drying process plates were closed by a lid with an outlet connected to a steel trap containing 150 mg Tenax TA and 150 mg Carbopack B (Markes International Ltd) and incubated at 28 °C. The Tenax steel traps were collected after three and five days of incubation and stored at 4 °C until GC-Q-TOF analysis. As controls, glass Petri-dishes containing LB agar media without inoculated bacteria or fungi were used.
Sample Type:Fungal/bacterial volatiles
Collection Method:Tenax Trap
Collection Location:Wageningen, The Netherlands
Collection Frequency:3 days and 5 days
Collection Duration:5 min.
Storage Conditions:4℃
Collection Vials:Tenax
Storage Vials:Metal tubes
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