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MB Sample ID: SA246278

Local Sample ID:20210712_Palaemon_Branchie_M8_78_01_10986
Subject ID:SU002550
Subject Type:Other organism
Subject Species:Palaemon serratus
Taxonomy ID:645159
Age Or Age Range:Adults
Weight Or Weight Range:10g
Height Or Height Range:5cm
Gender:Male and female

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Subject:

Subject ID:SU002550
Subject Type:Other organism
Subject Species:Palaemon serratus
Taxonomy ID:645159
Age Or Age Range:Adults
Weight Or Weight Range:10g
Height Or Height Range:5cm
Gender:Male and female

Factors:

Local Sample IDMB Sample IDFactor Level IDLevel ValueFactor Name
20210712_Palaemon_Branchie_M8_78_01_10986SA246278FL030888GillsOrgan
20210712_Palaemon_Branchie_M8_78_01_10986SA246278FL030888Malesex

Collection:

Collection ID:CO002543
Collection Summary:Specimens of Palaemon serratus were collected by a professional fisherman (DYFLO) in February 2021, using special traps in the 2-nautical mile zone of the Cap of La Hève (Le Havre, Normandy, France). The collected prawns were returned to the laboratory within a maximum of 1 h, using 30 L-polypropylene tanks filled with artificial sea water (ASW; salinity of 33‰ from dissolution of TETRA SEA® salt, which is commonly used in maintenance of marine aquarium), in oxygenated conditions (Rollin et al., 2021). The prawns were transferred and kept into 80 L-aquariums that were connected to an ASW supply, and under constant aeration and filtration. Then, 10 mature males and gravid females (i.e. ovarian stage 4) of homogenous size (i.e. 8.5 ± 0.9 cm total length) and homogenous moult stage (i.e. D1’-D1’’) were anesthetized on ice and dissected. The gills, the nervous gland (i.e. eyestalks medulla and supra oesophageal ganglia), the muscle, the hepatopancreas and the gonads were weighted, individually frozen in liquid nitrogen and stored at -20°C.
Sample Type:Shrimp organs
Collection Method:Fishing net
Collection Location:Le Havre, France
Storage Conditions:-20℃
Storage Vials:eppendorfs

Treatment:

Treatment ID:TR002562
Treatment Summary:no treatment was applied. Individuals were anaesthetized and organs were collected, frozen and kept at -20°C prior to metabolite extraction.

Sample Preparation:

Sampleprep ID:SP002556
Sampleprep Summary:Metabolites were extracted from wet tissues with 75%-25% UHPLC methanol-water (with a ratio of 1 ml for 100 mg of fresh tissues), grinded mechanically (GLH850 OMNI) and sonicated with an ultrasonic probe (SONICS VibraCell, 130 Watt, 20 Khz, 60% amplitude) for 30 sec, twice. Samples were then centrifuged at 15,000 g for 10 min at 4°C and the supernatant collected and store at -20°C until mass spectrometry analysis.
Processing Storage Conditions:-20℃
Extract Storage:-20℃

Combined analysis:

Analysis ID AN004014
Analysis type MS
Chromatography type Reversed phase
Chromatography system Bruker ELUTE UHPLC
Column Thermo Acclaim Polar Advantage II (150 x 3mm,3um)
MS Type ESI
MS instrument type QTOF
MS instrument name Bruker Compact
Ion Mode POSITIVE
Units counts

Chromatography:

Chromatography ID:CH002965
Chromatography Summary:The metabolites were analysed by injection of 2 µL of the supernatants on an UHPLC (ELUTE, Bruker) using a Polar Advances II 2.5 pore C18 column (Thermo, Waltham, MA, USA) at a 300 µL·min−1 flow rate with a linear gradient of acetonitrile in 0.1% formic acid (5%–90% in 16 min).
Instrument Name:Bruker ELUTE UHPLC
Column Name:Thermo Acclaim Polar Advantage II (150 x 3mm,3um)
Column Temperature:40
Flow Gradient:5-90%
Flow Rate:0.3 mL/min
Solvent A:100% water
Solvent B:100% acetonitrile
Chromatography Type:Reversed phase

MS:

MS ID:MS003761
Analysis ID:AN004014
Instrument Name:Bruker Compact
Instrument Type:QTOF
MS Type:ESI
MS Comments:Metabolites were subsequently ionised and analysed using an electrospray ionization hybrid quadrupole time-of-flight high-resolution mass spectrometer (ESI-Qq-TOF Compact, Bruker) at 2 Hz speed on the 50–1500 m/z range on positive autoMS/MS mode between 2 and 8 Hz speed on the 50–1500 m/z range with information-dependent acquisition (IDA).
Ion Mode:POSITIVE
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