Summary of Study ST002770

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 PR001727. The data can be accessed directly via it's Project DOI: 10.21228/M8GD9S This work is supported by NIH grant, U2C- DK119886.

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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 IDST002770
Study TitleMetabolomics and Molecular Networking-Guided Screening of Bacillus-Derived Bioactive Compounds Against a Highly Lethal Vibrio Species
Study SummaryDuring our search for active substances capable of inhibiting a newly discovered highly lethal Vibrio strain vp-HL causing highly lethal Vibrio disease in shrimp (HLVD), we found that the fermentation broth of multiple Bacillus strains exhibited antibacterial activity. However, the substances responsible for the activity remained unclear. Metabolomics was employed in conjunction with bioactivity screening to identify the antibacterial compounds from Bacillus strains. The Ethyl Acetate extracts of the broth of 20 Bacillus strains were analyzed using UPLC-MS/MS. Principal Component Analysis (PCA) and Orthogonal Partial Least Square - Discriminant Analysis (OPLS-DA) was used for pattern recognition. The strains fall into two groups in the scores plot from PCA. The S-plot from OPLS-DA offered information on biomarkers.
Institute
Third Institute of Oceanography, Ministry of Natural Resources
Last NameXia
First NameJinmei
AddressDaxue Rd, Xiamen, China.
Emailxiajinmei@tio.org.cn
Phone13003995626
Submit Date2023-06-29
Raw Data AvailableYes
Raw Data File Type(s)mzML
Analysis Type DetailLC-MS
Release Date2023-11-01
Release Version1
Jinmei Xia Jinmei Xia
https://dx.doi.org/10.21228/M8GD9S
ftp://www.metabolomicsworkbench.org/Studies/ application/zip

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Project:

Project ID:PR001727
Project DOI:doi: 10.21228/M8GD9S
Project Title:Bacillus-Derived Compounds Against a Vibrio
Project Summary:Metabolomics was employed in conjunction with bioactivity screening to identify the antibacterial compounds from Bacillus strains against the highly lethal Vibrio strain vp-HL.
Institute:Third Institute of Oceanography, Ministry of Natural Resources
Last Name:Xia
First Name:Jinmei
Address:Daxue Rd, Xiamen, China.
Email:xiajinmei@tio.org.cn
Phone:13003995626

Subject:

Subject ID:SU002877
Subject Type:Bacteria
Subject Species:Bacillus pumilus

Factors:

Subject type: Bacteria; Subject species: Bacillus pumilus (Factor headings shown in green)

mb_sample_id local_sample_id Group
SA29430424B1
SA29430527B1
SA2943062B1
SA29430722B1
SA29430823B1
SA29430920B1
SA2943104B1
SA29431114B1
SA2943127B1
SA29431315B1
SA29431447B2
SA29431550B2
SA29431656B2
SA29431746B2
SA29431834B2
SA29431935B2
SA29432038B2
SA29432139B2
SA29432243B2
SA29432344B2
Showing results 1 to 20 of 20

Collection:

Collection ID:CO002870
Collection Summary:The broth cultures were centrifuged at 7000 rpm for 10 min under 4 °C and the supernatants were collected.
Sample Type:Bacterial cells

Treatment:

Treatment ID:TR002886
Treatment Summary:The full-length 16S rRNA gene sequence was obtained for the studied Bacillus strains. The phylogenetic tree of the 16S rRNA gene showed that the strains formed two groups, which were defined as Group B1 and B2. The antagonistic activities of the Bacillus broth against the vp-HL strain were evaluated by the agar well diffusion method. The DI (diameters of the inhibition zones) values of the 20 Bacillus strains against the vp-HL strain were measured. All strains belonging to Group B2 showed DI values greater than those of strains from Group B1.

Sample Preparation:

Sampleprep ID:SP002883
Sampleprep Summary:The broth cultures were centrifuged at 7000 rpm for 10 min under 4 °C and the supernatants were collected. Ethyl acetate (EtOAc) with 2 × volume was added and sonicated for 10 min. The samples were then centrifuged at 7000 rpm at 4 °C for 10 min and the organic phase was collected and dried using a rotary evaporator. The extracts were resuspended in 1:1 acetonitrile: H2O with 1% formic acid. These samples were diluted 20 times using methanol. All samples were filtrated through 0.22 µm syringe filters.

Combined analysis:

Analysis ID AN004507
Analysis type MS
Chromatography type Reversed phase
Chromatography system Waters Acquity
Column Waters ACQUITY UPLC BEH C18 (50 x 2.1mm,1.7um)
MS Type ESI
MS instrument type QTOF
MS instrument name Waters Vion IMS QTof
Ion Mode POSITIVE
Units intensity

Chromatography:

Chromatography ID:CH003387
Chromatography Summary:Low pH polar
Instrument Name:Waters Acquity
Column Name:Waters ACQUITY UPLC BEH C18 (50 x 2.1mm,1.7um)
Column Temperature:30
Flow Gradient:5%B was kept for 0.5 min, 0.5-2.5 min, 5% to 30% B; 2.5-3.5 min, 30% to 40% B; 3.5-9 min, 40% to 99% B; 9-10 min, 99% to 5% B; and 5%B was kept for 3 min.
Flow Rate:0.35 mL/min
Solvent A:Water with 0.1% (vol/vol) formic acid
Solvent B:Acetonitrile with 0.1% (vol/vol) formic acid
Chromatography Type:Reversed phase

MS:

MS ID:MS004254
Analysis ID:AN004507
Instrument Name:Waters Vion IMS QTof
Instrument Type:QTOF
MS Type:ESI
MS Comments:UNIFI software (v. 1.8, Waters)
Ion Mode:POSITIVE
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