D-MALIC ACID PRODUCTION FROM DL-MALIC ACID BY ENANTIOSPECIFIC ASSIMILATION WITH ACINETOBACTER-LWOFII

被引:4
作者
MIYAMA, M
NAKAYAMA, K
机构
[1] Zama Research Laboratories, Bior Inc., Kanagawa, 5-5410, Zama
关键词
D O I
10.1007/BF00131547
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Acinetobacter lwofii ATCC 9036 assimilated L-malic acid eantiospecifically and left D-malic acid when grown in a medium containing DL-malic acid. The optical purity of the D-malic acid isolated from the culture filtrate was 100%. When the organism was incubated at 26-degrees-C, 220 r.p.m. in a Erlenmeyer flask containing 100g/l of disodium maleate, L-malic acid was completely consumed during 7 days incubation and D-malic acid remained at the concentration of 35g/l.
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页码:23 / 28
页数:6
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共 6 条
[1]   The effect of citrate on the rotation of the molybdate complexes of malate, citramalate and isocitrate [J].
Krebs, HA ;
Eggleston, LV .
BIOCHEMICAL JOURNAL, 1943, 37 :334-338
[2]   ENANTIOSELECTIVE SYNTHESES OF 3-SUBSTITUTED 4-(ALKOXYCARBONYL)-2-AZETIDINONES FROM MALIC-ACID [J].
MILLER, MJ ;
BAJWA, JS ;
MATTINGLY, PG ;
PETERSON, K .
JOURNAL OF ORGANIC CHEMISTRY, 1982, 47 (25) :4928-4933
[3]  
MIYAMA, 1993, IN PRESS BIOTECHNOL, V6
[4]   PHEROMONE SYNTHESIS .24. SYNTHESIS OF OPTICALLY-ACTIVE FORMS OF IPSDIENOL AND IPSENOL - PHEROMONE COMPONENTS OF IPS BARK BEETLES [J].
MORI, K ;
TAKIGAWA, T ;
MATSUO, T .
TETRAHEDRON, 1979, 35 (08) :933-940
[5]   TOTAL SYNTHESIS OF OPTICALLY-ACTIVE INTEGERRIMINE, A 12-MEMBERED DILACTONIC PYRROLIZIDINE ALKALOID OF RETRONECINE TYPE .2. ENANTIOSELECTIVE SYNTHESIS OF (+)-RETRONECINE [J].
NIWA, H ;
MIYACHI, Y ;
OKAMOTO, O ;
UOSAKI, Y ;
YAMADA, K .
TETRAHEDRON LETTERS, 1986, 27 (38) :4605-4608
[6]   STEREOCHEMICAL BEHAVIOR IN THE BIOSYNTHESIS OF 2-OXO-PANTOLACTONE - SYNTHESIS OF STEREOSPECIFICALLY INDICATED PANTOLACTONE FROM MALIC-ACID [J].
WASMUTH, D ;
ARIGONI, D ;
SEEBACH, D .
HELVETICA CHIMICA ACTA, 1982, 65 (01) :344-352