
pmid: 14061731
Abstract Several β-substituted aspartic acid analogs were tested as growth inhibitors of Escherichia coli and Leuconostoc mesenteroides. Of the compounds tested, the two racemic pairs of β-hydroxyaspartic acid were shown to be the most active inhibitors of growth. In most instances, this antagonism was readily reversed by l -aspartic acid. In L. mesenteroides, however, d -aspartic acid appears to be a more effective reversal agent than the l isomer in alleviating the growth inhibition caused by dl -erythro-β-hydroxyaspartic acid. None of the β-substituted aspartic acid analogs tested supported growth of L. mesenteroides, a culture which requires preformed aspartic acid, in the absence of aspartic acid.
Pharmacology, Aspartic Acid, Bacteria, Antimetabolites, Research, Escherichia coli, Chemistry Techniques, Analytical, Leuconostoc
Pharmacology, Aspartic Acid, Bacteria, Antimetabolites, Research, Escherichia coli, Chemistry Techniques, Analytical, Leuconostoc
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