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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
1988-7-25
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pubmed:abstractText |
The kinetics, quantitative yield, and sequence of solute release during the extraction of allergenic substances from short ragweed (Ambrosia artemisiifolia) pollen were compared with a conventional batch-type method and the novel technique of pollen grain column chromatography. With the batch method, 14.6 +/- 1.7 mg of pollen solutes were eluted per 100 mg of dried defatted pollen in 1 minute; the 24-hour solute yield was 27.4 +/- 2.7 mg. With the column method, 3.7 +/- 1.3 mg of pollen solutes were eluted in 1 minute; the 24-hour solute yield was 29.3 +/- 2.1 mg. The kinetics of solute release with the column method were modeled as the simultaneous first-order elution of ragweed-pollen solutes into three hypothetical compartments. The theoretical initial solute concentration was 50 gm/L. The isoelectric focusing patterns, optical properties, distributions of enzymes, Ra5, and antigen E activities were consistent with the sequential separation of ragweed-pollen solutes and the three compartment model. Enzyme activities were eluted either maximally in the first minute (phosphatases and N-acetyl-beta-glucaminidase) or delayed until 10 minutes (leucine aminopeptidase). Ra5 was eluted rapidly, whereas antigen E was eluted during a more prolonged period. Pollen grain chromatography provides a simple, reproducible method for studying pollen solute release.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Acid Phosphatase,
http://linkedlifedata.com/resource/pubmed/chemical/Alkaline Phosphatase,
http://linkedlifedata.com/resource/pubmed/chemical/Allergens,
http://linkedlifedata.com/resource/pubmed/chemical/Amb a I protein, Ambrosia...,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, Plant,
http://linkedlifedata.com/resource/pubmed/chemical/Cell Extracts,
http://linkedlifedata.com/resource/pubmed/chemical/Esterases,
http://linkedlifedata.com/resource/pubmed/chemical/Phosphoric Monoester Hydrolases,
http://linkedlifedata.com/resource/pubmed/chemical/Plant Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/group 5 allergens, Ambrosia
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
0091-6749
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
81
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1126-34
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:2837503-Acid Phosphatase,
pubmed-meshheading:2837503-Alkaline Phosphatase,
pubmed-meshheading:2837503-Allergens,
pubmed-meshheading:2837503-Antigens, Plant,
pubmed-meshheading:2837503-Cell Extracts,
pubmed-meshheading:2837503-Chromatography,
pubmed-meshheading:2837503-Esterases,
pubmed-meshheading:2837503-Isoelectric Focusing,
pubmed-meshheading:2837503-Kinetics,
pubmed-meshheading:2837503-Phosphoric Monoester Hydrolases,
pubmed-meshheading:2837503-Plant Proteins,
pubmed-meshheading:2837503-Pollen,
pubmed-meshheading:2837503-Substrate Specificity
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pubmed:year |
1988
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pubmed:articleTitle |
Pollen grain column chromatography: quantitation and biochemical analysis of ragweed-pollen solutes.
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pubmed:affiliation |
Department of Medicine, Duke University, Durham, NC 27710.
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pubmed:publicationType |
Journal Article
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