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MB Sample ID: SA177202

Local Sample ID:S_545
Subject ID:SU001991
Subject Type:Human
Subject Species:Homo sapiens
Taxonomy ID:9606

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Subject:

Subject ID:SU001991
Subject Type:Human
Subject Species:Homo sapiens
Taxonomy ID:9606

Factors:

Local Sample IDMB Sample IDFactor Level IDLevel ValueFactor Name
S_545SA177202FL021960SampleSample type

Collection:

Collection ID:CO001984
Collection Summary:Infant stool samples were collected at home using provided diapers, sealed in a separate polyethylene bag and frozen in a home freezer or kept chilled until transport. Samples were transported in a cooler with ice packs and brought to the routine 6-week post-partum visit within 24 hours of collection. Stool samples remained frozen until processing where they were thawed at 4 °C. Using sterile applicators, 0.5–1 g of stool was aliquoted into trace element-free cryovial tubes and then frozen at −80 °C in a biorepository
Sample Type:Feces
Storage Conditions:-80℃

Treatment:

Treatment ID:TR002003
Treatment Summary:NA

Sample Preparation:

Sampleprep ID:SP001997
Sampleprep Summary:De-identified stool aliquots were shipped on dry ice and immediately stored at -80 °C for metabolomics analysis. Samples were randomized into batches. For each batch, samples were thawed and ~150mg of stool was transferred to MagNA Lyser tubes after recording the weight, Samples were then homogenized with 50% acetonitrile in water by using the Omni Bead Disruptor (Omni International, GA, USA). Homogenized samples were centrifuged at 16000 rcf and the supernatant was separated into another tube. An aliquot (1000 uL, 100 mg equivalent of fecal mass) was transferred into Eppendorf tube and lyophilized overnight. The dried extract was reconstituted in 700 uL of NMR master mix (containing 0.2M phosphate, 0.5 mM DSS-d6, and 0.2% sodium azide), vortexed on a multitube vortexer at speed 5 for 2 min and centrifuged at 16000 rcf for 5 min. A 600 µl aliquot of the supernatant was transferred into a pre-labeled 5mm NMR tube for data acquisition on a 700 MHz spectrometer. Additionally, study pooled samples (created from randomly selected study samples) and batch pooled quality control (QC) samples were generated from supernatants of study samples and aliquots of supernatants were dried and reconstituted similar to study samples described above, and used for QC purposes.
Sampleprep Protocol Filename:1. Dartmouth-Fecal Metabolomics_NMR_Batch2 Procedures
Processing Storage Conditions:4℃
Extraction Method:50% Acetonitrile in Water
Extract Storage:-80℃
Sample Resuspension:In phosphate buffer containing D2O

Analysis:

MB Sample ID:SA177202
Analysis ID:AN003111
Laboratory Name:Metabolomics and Exposome Lab at UNC Nutrition Research Institute
Analysis Type:NMR
Software Version:TopSpin 3.5
Operator Name:Wimal Pathmasiri
Detector Type:NMR
Data Format:fid, 1r
Results File:4a._Dartmouth-Fecal_Metabolomics_NMR_Normalized_Binned_Data.txt
Units:ppm

NMR:

NMR ID:NM000214
Analysis ID:AN003111
Instrument Name:Avance III 700 MHz NMR Spectrometer
Instrument Type:FT-NMR
NMR Experiment Type:1D-1H
Field Frequency Lock:3015 Hz, D2O
Standard Concentration:0.5 mM
Spectrometer Frequency:700 MHz
NMR Probe:CP QCI/HPCN
NMR Solvent:90% H2O, 10% D2O
NMR Tube Size:5 mm
Shimming Method:topshim
Pulse Sequence:noesygppr1d
Water Suppression:pre-saturation
Pulse Width:14.59 us
Power Level:12.3 Watts
Receiver Gain:36
Offset Frequency:3290.61 Hz
Presaturation Power Level:0.0000964 Watts
Chemical Shift Ref Cpd:DSS-d6
Temperature:25 C
Number Of Scans:64
Dummy Scans:4
Acquisition Time:3.9 seconds
Relaxation Delay:2 seconds
Spectral Width:12 ppm
Num Data Points Acquired:65536
Real Data Points:32768
Line Broadening:0.5 Hz
Zero Filling:Yes
Apodization:Lorentzian
Baseline Correction Method:Polynomial
Chemical Shift Ref Std:DSS-d6
Binned Increment:0.04ppm
Binned Data Excluded Range:4.79 - 4.85 ppm (Water region)
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