#METABOLOMICS WORKBENCH TruxalCarlson_20200909_105704 DATATRACK_ID:2158 STUDY_ID:ST001480 ANALYSIS_ID:AN002457 PROJECT_ID:PR001004
VERSION             	1
CREATED_ON             	September 14, 2020, 4:17 pm
#PROJECT
PR:PROJECT_TITLE                 	Large diversity in nitrogen- and sulfur-containing compatible solute profiles in
PR:PROJECT_TITLE                 	polar and temperate diatoms
PR:PROJECT_TYPE                  	Marine Metabolomics
PR:PROJECT_SUMMARY               	Intense bottom-ice algal blooms, often dominated by diatoms, are an important
PR:PROJECT_SUMMARY               	source of food for grazers, organic matter for export during sea ice melt, and
PR:PROJECT_SUMMARY               	dissolved organic carbon. Sea-ice diatoms have a number of adaptations,
PR:PROJECT_SUMMARY               	including accumulation of compatible solutes, that allow them to inhabit this
PR:PROJECT_SUMMARY               	highly variable environment characterized by extremes in temperature, salinity,
PR:PROJECT_SUMMARY               	and light. In addition to protecting them from extreme conditions, these
PR:PROJECT_SUMMARY               	compounds present a labile, nutrient-rich source of organic matter and include
PR:PROJECT_SUMMARY               	precursors to climate active compounds (e.g. DMS), which are likely regulated
PR:PROJECT_SUMMARY               	with environmental change. Here, intracellular concentrations of 45 metabolites
PR:PROJECT_SUMMARY               	were quantified in three sea-ice diatom species and were compared to two
PR:PROJECT_SUMMARY               	temperate diatom species, with a focus on compatible solutes and free amino acid
PR:PROJECT_SUMMARY               	pools. There was a large diversity of metabolite concentrations between diatoms
PR:PROJECT_SUMMARY               	with no clear pattern identifiable for sea-ice species. Concentrations of some
PR:PROJECT_SUMMARY               	compatible solutes (isethionic acid, homarine) approached 1 M in the sea-ice
PR:PROJECT_SUMMARY               	diatoms, Fragilariopsis cylindrus and Navicula cf. perminuta, but not in the
PR:PROJECT_SUMMARY               	larger sea-ice diatom, Nitzschia lecointei or in the temperate diatom species.
PR:PROJECT_SUMMARY               	The differential use of compatible solutes in sea-ice diatoms suggest different
PR:PROJECT_SUMMARY               	adaptive strategies and highlights which small organic compounds may be
PR:PROJECT_SUMMARY               	important in polar biogeochemical cycles.
PR:INSTITUTE                     	University of Washington
PR:DEPARTMENT                    	Oceanography
PR:LABORATORY                    	Ingalls Lab
PR:LAST_NAME                     	Dawson
PR:FIRST_NAME                    	Hannah
PR:ADDRESS                       	1501 NE Boat Street, Marine Science Building, Room G, Seattle, WA, 98195, USA
PR:EMAIL                         	hmdawson@uw.edu
PR:PHONE                         	206-543-0744
PR:PUBLICATIONS                  	Dawson et al, 2020, Integrative and Comparative Biology
#STUDY
ST:STUDY_TITLE                   	Large diversity in nitrogen- and sulfur-containing compatible solute profiles in
ST:STUDY_TITLE                   	polar and temperate diatoms
ST:STUDY_TYPE                    	Intracellular metabolites were quantified in diatom species
ST:STUDY_SUMMARY                 	Intense bottom-ice algal blooms, often dominated by diatoms, are an important
ST:STUDY_SUMMARY                 	source of food for grazers, organic matter for export during sea ice melt, and
ST:STUDY_SUMMARY                 	dissolved organic carbon. Sea-ice diatoms have a number of adaptations,
ST:STUDY_SUMMARY                 	including accumulation of compatible solutes, that allow them to inhabit this
ST:STUDY_SUMMARY                 	highly variable environment characterized by extremes in temperature, salinity,
ST:STUDY_SUMMARY                 	and light. In addition to protecting them from extreme conditions, these
ST:STUDY_SUMMARY                 	compounds present a labile, nutrient-rich source of organic matter and include
ST:STUDY_SUMMARY                 	precursors to climate active compounds (e.g. DMS), which are likely regulated
ST:STUDY_SUMMARY                 	with environmental change. Here, intracellular concentrations of 45 metabolites
ST:STUDY_SUMMARY                 	were quantified in three sea-ice diatom species and were compared to two
ST:STUDY_SUMMARY                 	temperate diatom species, with a focus on compatible solutes and free amino acid
ST:STUDY_SUMMARY                 	pools. There was a large diversity of metabolite concentrations between diatoms
ST:STUDY_SUMMARY                 	with no clear pattern identifiable for sea-ice species. Concentrations of some
ST:STUDY_SUMMARY                 	compatible solutes (isethionic acid, homarine) approached 1 M in the sea-ice
ST:STUDY_SUMMARY                 	diatoms, Fragilariopsis cylindrus and Navicula cf. perminuta, but not in the
ST:STUDY_SUMMARY                 	larger sea-ice diatom, Nitzschia lecointei or in the temperate diatom species.
ST:STUDY_SUMMARY                 	The differential use of compatible solutes in sea-ice diatoms suggest different
ST:STUDY_SUMMARY                 	adaptive strategies and highlights which small organic compounds may be
ST:STUDY_SUMMARY                 	important in polar biogeochemical cycles.
ST:INSTITUTE                     	University of Washington
ST:DEPARTMENT                    	Oceanography
ST:LABORATORY                    	Ingalls Lab
ST:LAST_NAME                     	Dawson
ST:FIRST_NAME                    	Hannah
ST:ADDRESS                       	1501 NE Boat Street, Marine Science Building, Room G, Seattle, WA, 98195, USA
ST:EMAIL                         	hmdawson@uw.edu
ST:PHONE                         	206-543-0744
ST:PUBLICATIONS                  	Dawson et al, 2020, Integrative and Comparative Biology
#SUBJECT
SU:SUBJECT_TYPE                  	Other
SU:SUBJECT_SPECIES               	Nitzschia lecointei;Fragilariopsis cylindrus;Navicula cf. perminuta;Navicula pelliculosa
#SUBJECT_SAMPLE_FACTORS:         	SUBJECT(optional)[tab]SAMPLE[tab]FACTORS(NAME:VALUE pairs separated by |)[tab]Raw file names and additional sample data
SUBJECT_SAMPLE_FACTORS           	-	Nl_32ppt-1C_1	Species:Nitzschia lecointei | Salinity:32 | Temp_degC:-1	Light=Saturating; Cobalamin=Replete; Vol_intracellular_µL=1.2756163; Vol_filtered_mL=70; Replicate=1; Type=Smp; Strain=NA; RAW_FILE_NAME=200309_Smp_32ppt-1C_A 200309_Smp_32ppt-1C_A
SUBJECT_SAMPLE_FACTORS           	-	Nl_32ppt-1C_2	Species:Nitzschia lecointei | Salinity:32 | Temp_degC:-1	Light=Saturating; Cobalamin=Replete; Vol_intracellular_µL=1.174789; Vol_filtered_mL=70; Replicate=2; Type=Smp; Strain=NA; RAW_FILE_NAME=200309_Smp_32ppt-1C_B 200309_Smp_32ppt-1C_
SUBJECT_SAMPLE_FACTORS           	-	Nl_32ppt-1C_3	Species:Nitzschia lecointei | Salinity:32 | Temp_degC:-1	Light=Saturating; Cobalamin=Replete; Vol_intracellular_µL=1.1610501; Vol_filtered_mL=70; Replicate=3; Type=Smp; Strain=NA; RAW_FILE_NAME=200309_Smp_32ppt-1C_C 200309_Smp_32ppt-1C_C
SUBJECT_SAMPLE_FACTORS           	-	Nl_32ppt4C_1	Species:Nitzschia lecointei | Salinity:32 | Temp_degC:4	Light=Saturating; Cobalamin=Replete; Vol_intracellular_µL=1.532752987; Vol_filtered_mL=70; Replicate=1; Type=Smp; Strain=NA; RAW_FILE_NAME=200309_Smp_32ppt4C_A 200309_Smp_32ppt4C_A
SUBJECT_SAMPLE_FACTORS           	-	Nl_32ppt4C_2	Species:Nitzschia lecointei | Salinity:32 | Temp_degC:4	Light=Saturating; Cobalamin=Replete; Vol_intracellular_µL=1.75542558; Vol_filtered_mL=70; Replicate=2; Type=Smp; Strain=NA; RAW_FILE_NAME=200309_Smp_32ppt4C_B 200309_Smp_32ppt4C_B
SUBJECT_SAMPLE_FACTORS           	-	Nl_32ppt4C_3	Species:Nitzschia lecointei | Salinity:32 | Temp_degC:4	Light=Saturating; Cobalamin=Replete; Vol_intracellular_µL=1.66524318; Vol_filtered_mL=70; Replicate=3; Type=Smp; Strain=NA; RAW_FILE_NAME=200309_Smp_32ppt4C_C 200309_Smp_32ppt4C_C
SUBJECT_SAMPLE_FACTORS           	-	Nl_41ppt-1C_1	Species:Nitzschia lecointei | Salinity:41 | Temp_degC:-1	Light=Saturating; Cobalamin=Replete; Vol_intracellular_µL=1.746388756; Vol_filtered_mL=70; Replicate=1; Type=Smp; Strain=NA; RAW_FILE_NAME=200309_Smp_41ppt-1C_A 200309_Smp_41ppt-1C_A
SUBJECT_SAMPLE_FACTORS           	-	Nl_41ppt-1C_2	Species:Nitzschia lecointei | Salinity:41 | Temp_degC:-1	Light=Saturating; Cobalamin=Replete; Vol_intracellular_µL=1.399316304; Vol_filtered_mL=70; Replicate=2; Type=Smp; Strain=NA; RAW_FILE_NAME=200309_Smp_41ppt-1C_B 200309_Smp_41ppt-1C_B
SUBJECT_SAMPLE_FACTORS           	-	Nl_41ppt-1C_3	Species:Nitzschia lecointei | Salinity:41 | Temp_degC:-1	Light=Saturating; Cobalamin=Replete; Vol_intracellular_µL=1.657191524; Vol_filtered_mL=70; Replicate=3; Type=Smp; Strain=NA; RAW_FILE_NAME=200309_Smp_41ppt-1C_C 200309_Smp_41ppt-1C_C
SUBJECT_SAMPLE_FACTORS           	-	Nl_41ppt4C_1	Species:Nitzschia lecointei | Salinity:41 | Temp_degC:4	Light=Saturating; Cobalamin=Replete; Vol_intracellular_µL=1.11758985; Vol_filtered_mL=70; Replicate=1; Type=Smp; Strain=NA; RAW_FILE_NAME=200309_Smp_41ppt4C_A 200309_Smp_41ppt4C_A
SUBJECT_SAMPLE_FACTORS           	-	Nl_41ppt4C_2	Species:Nitzschia lecointei | Salinity:41 | Temp_degC:4	Light=Saturating; Cobalamin=Replete; Vol_intracellular_µL=1.310557636; Vol_filtered_mL=70; Replicate=2; Type=Smp; Strain=NA; RAW_FILE_NAME=200309_Smp_41ppt4C_B 200309_Smp_41ppt4C_B
SUBJECT_SAMPLE_FACTORS           	-	Nl_41ppt4C_3	Species:Nitzschia lecointei | Salinity:41 | Temp_degC:4	Light=Saturating; Cobalamin=Replete; Vol_intracellular_µL=1.272660153; Vol_filtered_mL=70; Replicate=3; Type=Smp; Strain=NA; RAW_FILE_NAME=200309_Smp_41ppt4C_C 200309_Smp_41ppt4C_C
SUBJECT_SAMPLE_FACTORS           	-	Fc_1	Species:Fragilariopsis cylindrus | Salinity:31 | Temp_degC:-1	Light=Saturating; Cobalamin=Replete; Vol_intracellular_µL=0.232254; Vol_filtered_mL=69; Replicate=1; Type=Smp; Strain=CCMP1102; RAW_FILE_NAME=200309_Smp_Fc_1 200309_Smp_Fc_1
SUBJECT_SAMPLE_FACTORS           	-	Fc_2	Species:Fragilariopsis cylindrus | Salinity:31 | Temp_degC:-1	Light=Saturating; Cobalamin=Replete; Vol_intracellular_µL=0.23529; Vol_filtered_mL=69; Replicate=2; Type=Smp; Strain=CCMP1102; RAW_FILE_NAME=200309_Smp_Fc_2 200309_Smp_Fc_2
SUBJECT_SAMPLE_FACTORS           	-	Nl_1	Species:Nitzschia lecointei | Salinity:31 | Temp_degC:-1	Light=Saturating; Cobalamin=Replete; Vol_intracellular_µL=0.51129; Vol_filtered_mL=69; Replicate=1; Type=Smp; Strain=NA; RAW_FILE_NAME=200309_Smp_Nl_1 200309_Smp_Nl_1
SUBJECT_SAMPLE_FACTORS           	-	Nl_2	Species:Nitzschia lecointei | Salinity:31 | Temp_degC:-1	Light=Saturating; Cobalamin=Replete; Vol_intracellular_µL=0.490314; Vol_filtered_mL=69; Replicate=2; Type=Smp; Strain=NA; RAW_FILE_NAME=200309_Smp_Nl_2 200309_Smp_Nl_2
SUBJECT_SAMPLE_FACTORS           	-	Nperm_1	Species:Navicula cf. perminuta | Salinity:31 | Temp_degC:-1	Light=Saturating; Cobalamin=Replete; Vol_intracellular_µL=0.203895; Vol_filtered_mL=69; Replicate=1; Type=Smp; Strain=NA; RAW_FILE_NAME=200309_Smp_Np_1 200309_Smp_Np_1
SUBJECT_SAMPLE_FACTORS           	-	Nperm_2	Species:Navicula cf. perminuta | Salinity:31 | Temp_degC:-1	Light=Saturating; Cobalamin=Replete; Vol_intracellular_µL=0.193545; Vol_filtered_mL=69; Replicate=2; Type=Smp; Strain=NA; RAW_FILE_NAME=200309_Smp_Np_2 200309_Smp_Np_2
SUBJECT_SAMPLE_FACTORS           	-	Npell_1	Species:Navicula pelliculosa | Salinity:35 | Temp_degC:13	Light=Saturating; Cobalamin=Replete; Vol_intracellular_µL=0.6318675; Vol_filtered_mL=69; Replicate=1; Type=Smp; Strain=CCMP543; RAW_FILE_NAME=200309_Smp_NpB12SL_AB 200309_Smp_NpB12SL_AB
SUBJECT_SAMPLE_FACTORS           	-	Npell_2	Species:Navicula pelliculosa | Salinity:35 | Temp_degC:13	Light=Saturating; Cobalamin=Replete; Vol_intracellular_µL=0.6090975; Vol_filtered_mL=69; Replicate=2; Type=Smp; Strain=CCMP543; RAW_FILE_NAME=200309_Smp_NpB12SL_.D 200309_Smp_NpB12SL_CD
SUBJECT_SAMPLE_FACTORS           	-	Npell_3	Species:Navicula pelliculosa | Salinity:35 | Temp_degC:13	Light=Saturating; Cobalamin=Replete; Vol_intracellular_µL=0.59409; Vol_filtered_mL=69; Replicate=3; Type=Smp; Strain=CCMP543; RAW_FILE_NAME=200309_Smp_NpB12SL_EF 200309_Smp_NpB12SL_EF
#COLLECTION
CO:COLLECTION_SUMMARY            	Axenic cultures of three Antarctic sea-ice diatoms (N. lecointei, N. cf.
CO:COLLECTION_SUMMARY            	perminuta, and F. cylindrus) and two temperate diatoms (T. pseudonana and N.
CO:COLLECTION_SUMMARY            	pelliculosa) were chosen for study. Cells were harvested during exponential
CO:COLLECTION_SUMMARY            	growth onto 47 mm 0.2 µm PTFE filters (Omnipore) using combusted glassware and
CO:COLLECTION_SUMMARY            	gentle filtration and stored at –80 °C until extraction. For each biological
CO:COLLECTION_SUMMARY            	replicate (n = 2 for Antarctic species, n = 3 for temperate species), two 35 mL
CO:COLLECTION_SUMMARY            	cultures were harvested onto each filter . An un-inoculated media blank was
CO:COLLECTION_SUMMARY            	prepared and treated in the same manner as samples.
CO:SAMPLE_TYPE                   	Cultured diatom cells
CO:STORAGE_CONDITIONS            	Described in summary
#TREATMENT
TR:TREATMENT_SUMMARY             	Antarctic species were grown at −1°C and a PAR irradiance of 45 𝜇mol
TR:TREATMENT_SUMMARY             	photons m−2 s−1 (16:8 light:dark cycle) using cool white lights. Temperate
TR:TREATMENT_SUMMARY             	species were grown at 13°C and a PAR irradiance of 120 𝜇mol photons m−-2
TR:TREATMENT_SUMMARY             	s−-1(12:12 light:dark cycle). In both cases, light was saturating. Cultures
TR:TREATMENT_SUMMARY             	were grown in artificial seawater (ESAW, salinity 31, for Antarctic species and
TR:TREATMENT_SUMMARY             	Instant Ocean, salinity ~35 for temperate species). Cobalamin (vitamin B12) was
TR:TREATMENT_SUMMARY             	replete in all cultures. To explore the effect of growth conditions on metabolic
TR:TREATMENT_SUMMARY             	profiles using non-metric dimensional scaling analysis, samples were included of
TR:TREATMENT_SUMMARY             	N. lecointei grown at temperatures of −1 and 4˚C and salinities of 32 and 41.
#SAMPLEPREP
SP:SAMPLEPREP_SUMMARY            	Each sample was extracted using a modified Bligh-Dyer extraction. Briefly,
SP:SAMPLEPREP_SUMMARY            	filters were cut up and put into 15 mL teflon centrifuge tubes containing a
SP:SAMPLEPREP_SUMMARY            	mixture of 100 µm and 400 µm silica beads. Heavy isotope-labeled internal
SP:SAMPLEPREP_SUMMARY            	standards were added along with ~2 mL of cold aqueous solvent (50:50
SP:SAMPLEPREP_SUMMARY            	methanol:water) and ~3 mL of cold organic solvent (dichloromethane). The samples
SP:SAMPLEPREP_SUMMARY            	were shaken on a FastPrep-24 Homogenizer for 30 seconds and chilled in a -20 °C
SP:SAMPLEPREP_SUMMARY            	freezer repeatedly for three cycles of bead-beating and a total of 30 minutes of
SP:SAMPLEPREP_SUMMARY            	chilling. The organic and aqueous layers were separated by spinning samples in a
SP:SAMPLEPREP_SUMMARY            	centrifuge at 4,300 rpm for 2 minutes at 4 °C. The aqueous layer was removed to
SP:SAMPLEPREP_SUMMARY            	a new glass centrifuge tube. The remaining organic fraction was rinsed three
SP:SAMPLEPREP_SUMMARY            	more times with additions of 1 to 2 mL of 50:50 methanol:water. All aqueous
SP:SAMPLEPREP_SUMMARY            	rinses were combined for each sample and dried down under N2 gas. The remaining
SP:SAMPLEPREP_SUMMARY            	organic layer was transferred into a clean glass centrifuge tube and the
SP:SAMPLEPREP_SUMMARY            	remaining bead beating tube was rinsed two more times with cold organic solvent.
SP:SAMPLEPREP_SUMMARY            	The combined organic rinses were centrifuged, transferred to a new tube, and
SP:SAMPLEPREP_SUMMARY            	dried under N2 gas. Dried aqueous fractions were re-dissolved in 380 µL of
SP:SAMPLEPREP_SUMMARY            	water. Dried organic fractions were re-dissolved in 380 µL of 1:1
SP:SAMPLEPREP_SUMMARY            	water:acetonitrile. 20 µL of isotope-labeled injection standards in water were
SP:SAMPLEPREP_SUMMARY            	added to both fractions. An un-inoculated media blank was prepared and treated
SP:SAMPLEPREP_SUMMARY            	in the same manner as the samples.
SP:PROCESSING_STORAGE_CONDITIONS 	On ice
SP:EXTRACTION_METHOD             	Bligh-Dyer
SP:EXTRACT_STORAGE               	-80℃
#CHROMATOGRAPHY
CH:CHROMATOGRAPHY_SUMMARY        	See attached summary.
CH:CHROMATOGRAPHY_TYPE           	HILIC
CH:INSTRUMENT_NAME               	Waters Acquity I-Class
CH:COLUMN_NAME                   	SeQuant ZIC- pHILIC (150 x 2.1mm, 5um)
#ANALYSIS
AN:ANALYSIS_TYPE                 	MS
#MS
MS:INSTRUMENT_NAME               	Thermo Q Exactive HF hybrid Orbitrap
MS:INSTRUMENT_TYPE               	Orbitrap
MS:MS_TYPE                       	ESI
MS:ION_MODE                      	NEGATIVE
MS:MS_COMMENTS                   	See attached protocol.
#MS_METABOLITE_DATA
MS_METABOLITE_DATA:UNITS	mM (intracellular concentration)
MS_METABOLITE_DATA_START
Samples	Fc_1	Fc_2	Nperm_1	Nperm_2	Nl_1	Nl_2	Nl_32ppt-1C_1	Nl_32ppt-1C_2	Nl_32ppt-1C_3	Nl_32ppt4C_1	Nl_32ppt4C_2	Nl_32ppt4C_3	Nl_41ppt-1C_1	Nl_41ppt-1C_2	Nl_41ppt-1C_3	Nl_41ppt4C_1	Nl_41ppt4C_2	Nl_41ppt4C_3	Npell_1	Npell_2	Npell_3
Factors	Species:Fragilariopsis cylindrus | Salinity:31 | Temp_degC:-1	Species:Fragilariopsis cylindrus | Salinity:31 | Temp_degC:-1	Species:Navicula cf. perminuta | Salinity:31 | Temp_degC:-1	Species:Navicula cf. perminuta | Salinity:31 | Temp_degC:-1	Species:Nitzschia lecointei | Salinity:31 | Temp_degC:-1	Species:Nitzschia lecointei | Salinity:31 | Temp_degC:-1	Species:Nitzschia lecointei | Salinity:32 | Temp_degC:-1	Species:Nitzschia lecointei | Salinity:32 | Temp_degC:-1	Species:Nitzschia lecointei | Salinity:32 | Temp_degC:-1	Species:Nitzschia lecointei | Salinity:32 | Temp_degC:4	Species:Nitzschia lecointei | Salinity:32 | Temp_degC:4	Species:Nitzschia lecointei | Salinity:32 | Temp_degC:4	Species:Nitzschia lecointei | Salinity:41 | Temp_degC:-1	Species:Nitzschia lecointei | Salinity:41 | Temp_degC:-1	Species:Nitzschia lecointei | Salinity:41 | Temp_degC:-1	Species:Nitzschia lecointei | Salinity:41 | Temp_degC:4	Species:Nitzschia lecointei | Salinity:41 | Temp_degC:4	Species:Nitzschia lecointei | Salinity:41 | Temp_degC:4	Species:Navicula pelliculosa | Salinity:35 | Temp_degC:13	Species:Navicula pelliculosa | Salinity:35 | Temp_degC:13	Species:Navicula pelliculosa | Salinity:35 | Temp_degC:13
Cysteic Acid	0.220308128	0.180471397	38.93058894	47.73955314	1.79630068	2.573834052	0.451618071	0.49157852	0.483654448	0.322380339	0.257077757	0.432169789	0.213342879	0.280651409	0.236813466	0.370011503	0.276918049	0.274553617			
DHPS			205.1945008	217.5637618	71.32511869	80.4518594	34.66824326	33.18666562	41.31862866	29.22191195	23.47146157	32.21356354	32.75438582	40.3458025	35.1679633	63.83991191	33.39737247	34.59442417	7.191210725	3.069111334	2.810251636
Isethionic Acid	1036.940614	909.4273807	0.333396755	0.188736694	1.559017281	0.313406235	0.02400944	0.022469527	0.023298774	0.050380358	0.044745878	0.048401826				0.042865604	0.035874663	0.027861386			
L-Pyroglutamic acid	2.568606578	2.212950335	10.49756325	13.55793016	1.871343159	2.60337302	0.908882395	0.95367034	1.186045876	0.377215007	0.386287727	0.59671078	0.749597316	0.829637875	0.759777659	0.643583351	0.418551353	0.596552437	21.11499564	13.52200313	12.79691343
Sucrose							0.036684942		0.043287353	0.028184314	0.104058566	0.040666763	0.135520841	0.041580783	0.052382281	0.178537884	0.061821958	0.28590915			
Sulfolactic Acid	0.003837326	0.007451488	0.004441515	0.006770601	0.036844077	0.042405272	0.003984052	0.005242126	0.01558195	0.030448103	0.027774478	0.053616041	0.008838588	0.007004662	0.009488644	0.061659192	0.046209417	0.039208448			
Taurine	342.9803485	341.5099969			0.53981803	0.122821752	0.088859694	0.104881747	0.105480207	0.378777795	0.360269576	0.347204642	0.092183839	0.119254789	0.104301346	0.43884965	0.351090828	0.278562739			
Trehalose			0.0505798	0.064189205			0.00312502	0.023300023	0.007525223	0.005173465	0.012639175	0.010232693	0.0156806	0.013538649		0.015893105	0.012209089	0.01632141			
MS_METABOLITE_DATA_END
#METABOLITES
METABOLITES_START
metabolite_name	quantitated m/z	KEGG_ID	CHEBI	KEGGNAME	MS_method
Cysteic Acid	167.996671	C00506	CHEBI:17285	L-Cysteate; L-Cysteic acid; 3-Sulfoalanine; 2-Amino-3-sulfopropionic acid	HILIC_QE_Neg
DHPS	155.001422	C19675	CHEBI:60997	(R)-2,3-Dihydroxypropane-1-sulfonate	HILIC_QE_Neg
Isethionic Acid	124.990857	C05123	CHEBI:1157	2-Hydroxyethanesulfonate; 2-Hydroxyethanesulfonic acid; 2-Hydroxyethane-1-sulfonic acid; Isethionic acid; Isethionate	HILIC_QE_Neg
L-Pyroglutamic acid	128.034768	C01879	CHEBI:18183	5-Oxoproline; Pidolic acid; Pyroglutamic acid; 5-Pyrrolidone-2-carboxylic acid; Pyroglutamate; 5-Oxo-L-proline; L-Pyroglutamic acid; L-5-Pyrrolidone-2-carboxylic acid	HILIC_QE_Neg
Sucrose	341.10839	C00089	CHEBI:17992	Sucrose; Cane sugar; Saccharose; 1-alpha-D-Glucopyranosyl-2-beta-D-fructofuranoside	HILIC_QE_Neg
Sulfolactic Acid	168.980687	C16069	CHEBI:50519	3-Sulfolactate	HILIC_QE_Neg
Taurine	124.006841	C00245	CHEBI:15891	Taurine; 2-Aminoethanesulfonic acid; Aminoethylsulfonic acid	HILIC_QE_Neg
Trehalose	341.10839	C01083	CHEBI:16551	alpha,alpha-Trehalose; alpha,alpha'-Trehalose; Trehalose	HILIC_QE_Neg
METABOLITES_END
#END