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Metabolites detected in the spent supernatant after growth of salmon gut-derived bacteria on chitin and mannotetraose

ABSTRACT: Bacteria were grown on a minimal medium supplemented with chitin or mannotetraose as a sole carbon source. Cell pellet was removed and supernatant analysed for untargeted metabolomics. The sample was prepared by pooling small equal aliquots from each sample, to create a representative average of the entire set.

INSTRUMENT(S): Orbitrap Exploris 240

ORGANISM(S): Serratia Liquefaciens (ncbitaxon:614) Vibrio Splendidus (ncbitaxon:29497) Pseudomonas Sp. (ncbitaxon:306) Lelliottia Amnigena (ncbitaxon:61646) Carnobacterium Maltaromaticum (ncbitaxon:2751) Photobacterium Phosphoreum (ncbitaxon:659) Flavobacterium Sp. (ncbitaxon:239)

SUBMITTER: Sabina Leanti La Rosa/Phil B. Pope

PROVIDER: MSV000094616 | MassIVE | Thu Apr 25 00:44:00 BST 2024

REPOSITORIES: MassIVE

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Project description:One µg of total RNA from either an individual rat or from a pooled sample was amplified and labeled with a fluorescent dye (either Cy3 or Cy5) using the Low RNA Input Linear Amplification Labeling kit (Agilent Technologies, Palo Alto, CA) following the manufacturer’s protocol. The amount and quality of the resulting fluorescently labeled cRNA was assessed using a Nanodrop ND-100 spectrophometer and an Agilent Bioanalyzer. Equal amounts of Cy3- or Cy5-labeled cRNA were hybridized to the Agilent Rat Oligo Microarray (Agilent Technologies, Inc., Palo Alto, CA) for 17 hrs, prior to washing and scanning. Data was extracted from the resulting images using Agilent’s Feature Extraction Software (Agilent Technologies, Inc., Palo Alto, CA). For day/night comparisons, two types of complementing hybridizations were performed: hepatic RNA from individual day rats was hybridized against a pool made up of RNA from 12 hour offset night rats, and RNA from individual night rats was hybridized against a pool made up of RNA from 12-hour offset day rats. Specifically, hepatic RNA samples from three individual day rats collected ten hours after light on (CT10) were hybridized against a pooled RNA sample composed of equal aliquots of RNA from the livers of six night rats collected ten hrs after lights off (CT22); and RNA samples from three individual night rats collected at CT22 were hybridized against a pooled RNA sample composed of equal aliquots of RNA from the livers of six day rats collected at CT10. This was replicated in a second study for a total of 24 hybridizations of 12 hour offset samples. For time of day comparisons, equal aliquots of RNA from the livers of six rats collected at each of four different times of the circadian day (CT4, CT10, C16 and CT22) were pooled. The two replicate studies thus resulted in 8 pools (two replicate pools/time point times four time points); each pool was hybridized against a Universal Rat Reference RNA Standard (Stratagene, La Jolla, CA). Keywords: time-course

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Metabolites detected in the spent supernatant after growth of salmon gut-derived bacteria on chitin and mannotetraose

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