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   <subfield code="a">Asymmetric amination of 4-methoxyphenylacetone and its related compounds with microorganisms</subfield>
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   <subfield code="c">[Katsuhiko Nakamichi, Takeji Shibatani, Yoko Yamamoto, Tadashi Sato]</subfield>
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   <subfield code="a">Summary: Asymmetric amination of 4-methoxyphenylacetone and its related compounds by microorganisms was investigated. Among 630 type culture strains, 4-methoxyphenylacetone-aminating ability was found inBrevibacterium, Chromobacterium, Flavobacterium, Mycobacterium, Pseudomonas, andSarcina spp. 4-Methoxyamphetamine produced by these microorganisms was the (S)-(+)-enantiomer.B. linens IFO 12141 was selected as the best strain. The optimum pH of amination was about 7.0, andl-alanine was the most effective aminov donor for the amination. By using this strain, 37.6 mM (S)-(+)-4-methoxyamphetamine was formed with a 94% conversion yield from 4-methoxyphenylacetone. As for substrate specificity,B. linens IFO 12141 catalysed amination of 3,4-dimethoxyphenylacetone and 4-(4-methoxyphenyl)-2-butanone, and formed the corresponding optically active amines.</subfield>
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