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A method for the isolation of canavanine by ion exchange

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Title A method for the isolation of canavanine by ion exchange
Names Fujiwara, Allan (creator)
Christensen, Bert E. (advisor)
Date Issued 1964-09-22 (iso8601)
Note Graduation date: 1965
Abstract In 1959 Kitagawa discovered and isolated the amino acid,
canavanine. Since its discovery much interest has been centered on
this amino acid because of its biological aspects; e.g. canavanine has
been shown to inhibit the growth of bacteria, viruses, protozoa, and
cancer cells.
The occurrence of canavanine is widespread in the leguminous
plants and its identification and isolation for this reason has been restricted
to these plants; of the leguminous plants, jack bean meal
(Canavalia ensiformis) has been a readily available source.
The most notable of its properties is the characteristic ruby
red color which canavanine forms with sodium nitroprusside. This
color formation has been used for the identification of canavanine in
natural products. An unfortunate reaction of canavanine is its deamination
and cyclization to desaminocanavanine under neutral conditions.
This conversion has been responsible for some of the loss of canavanine during its isolation. A, useful reaction which canavanine
undergoes is the formation of an insoluble salt with flavianic
acid. The formation of canavanine diflavianate is the usual method
for the isolation of canavanine from crude extraction mixtures. However,
various workers have experienced difficulty in the conversion
of canavanine diflavianate to its free base and thus they have introduced
various modifications in the procedure. The author in attempting
to isolate canavanine from the crude extracts by the use of flavianic
acid has also found the conversion of canavanine diflavianate to
its free base (canavanine) difficult and tedious. It was found that in
order to effect a complete conversion, a large excess of barium hydroxide
must be added to an incipient boiling solution of canavanine
diflavianate. Under these conditions a reliable isolation of canavanine
was obtained.
Since the use of flavianic acid in the isolation of canavanine
has proved to be difficult and tedious an ion exchange method which
avoids the use of flavianic acid has been investigated. The results
with this method indicated that a quantitative and practical isolation
of canavanine directly from the crude extracts could be achieved.
The use of a strongly acidic ion exchange resin in conjunction with a
preferential eluting agent has been the key for the separation and isolation
of canavanine as its free base from the impurities in the crude
extract.
Genre Thesis/Dissertation
Topic Amino acids
Identifier http://hdl.handle.net/1957/48142

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