2013
DOI: 10.1029/gm063p0151
|View full text |Cite
|
Sign up to set email alerts
|

Extraction and Analysis of Polysaccharides, Chiral Amino Acids, and Sfe-Extractable Lipids from Marine POM

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
2

Citation Types

0
7
0

Year Published

2016
2016
2023
2023

Publication Types

Select...
8

Relationship

0
8

Authors

Journals

citations
Cited by 16 publications
(7 citation statements)
references
References 36 publications
0
7
0
Order By: Relevance
“…The concentrations of D- and L-isomers of Asp were determined by the HPLC method described by Mopper and Furton (1991) with the modifications given in Langerhuus et al (2012) , including the following additional modifications: (1) N-isobutyryl-D-cysteine (IBDC) was used as a chiral agent added to OPA, (2) the pH of eluent A was adjusted to 6.4, (3) L-glutamine was used as an internal standard, and (4) all samples were analyzed twice, whereby one of the samples was spiked with a 25 nM standard. The concentrations of D- and L-aspartic acid were corrected for racemization during hydrolysis according to Kaiser and Benner (2005) .…”
Section: Methodsmentioning
confidence: 99%
“…The concentrations of D- and L-isomers of Asp were determined by the HPLC method described by Mopper and Furton (1991) with the modifications given in Langerhuus et al (2012) , including the following additional modifications: (1) N-isobutyryl-D-cysteine (IBDC) was used as a chiral agent added to OPA, (2) the pH of eluent A was adjusted to 6.4, (3) L-glutamine was used as an internal standard, and (4) all samples were analyzed twice, whereby one of the samples was spiked with a 25 nM standard. The concentrations of D- and L-aspartic acid were corrected for racemization during hydrolysis according to Kaiser and Benner (2005) .…”
Section: Methodsmentioning
confidence: 99%
“…Concentrations of D- and L-isomers of amino acids were analysed by HPLC following the method described by ref. 70 and with the modifications described in ref. 71 .…”
Section: Methods Summarymentioning
confidence: 99%
“…After gently inverting sub-sample bottles to homogenize, splits were filtered through 0.2 μm polypropylene filters for analysis of TDP and DIP. Samples were vacuum filtered using Nalgene ® polysulfone filtration apparatus at low pressure (≤5 psi) to prevent cell lysis (e.g., Bidigare, 1991; Karl et al, 1991; Matrai, 1991; Mopper and Furton, 1991). Filtration apparatus were acid cleaned (10% HCl) prior to initial use; between samples the upper reservoir was rinsed with unfiltered sample water, and the lower reservoir with the first 50-mL of filtrate to pass through the filter.…”
Section: Methodsmentioning
confidence: 99%