氨基酸抗代谢产物的研究。(八)微生物中精氨酸琥珀酸和菜豆琥珀酸的形成

Tomoji Suzuki, S. Muraoka, T. Makino
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引用次数: 3

摘要

氨基酸抗代谢产物的研究。(八)微生物精氨酸琥珀酸和菜豆琥珀酸的形成铃木智二、木保oka三郎和真野Teruo(铃木实验室)日本药学会杂志,77,282(1957)制备了大肠杆菌和阿拉伯乳杆菌的丙酮干燥细胞,用纸电泳和纸层析法观察了精氨酸或菜豆琥珀酸和富马酸形成精氨酸琥珀酸(ASA)和菜豆琥珀酸(CSA)。ASA是由大肠杆菌亲本菌株形成的,但没有检测到其需要精氨酸的突变体(不能用鸟氨酸或瓜氨酸来补偿)。即使是亲本菌株,在含有精氨酸的培养基中培养也会导致精氨酸琥珀酸酶活性消失,也不会形成ASA。CSA的形成与ASA相同。注射。阿拉伯糖ASA是由瓜氨酸和天冬氨酸以及精氨酸和富马酸形成的。CSA本身抑制Lact的增殖。这种抑制作用很容易用精氨酸恢复。从实验结果出发,对大麻碱的作用机理进行了探讨。氨基酸抗代谢产物的研究。(九)天冬氨酸单、二肼的生物活性铃木智司和田中文彦(铃木实验室)日本药学会学报,77,1218(1957)合成了天冬氨酸单、二肼和3-羟基天冬氨酸,并研究了它们对肠系膜白孢菌P-60和大肠杆菌1号的抑制作用。在天冬氨酸存在的情况下,白细胞的生长。肠系膜被100 r/cc完全抑制。单肼,500r /cc。3-羟基天冬氨酸,2000 r/cc。肼。到留伊克为止。因此,单肼的生长抑制作用强于双肼。相反,不需要天冬氨酸的大肠杆菌1号的生长被二肼更强烈地抑制,509的有效抑制浓度为55 r/cc。单肼和33 r/cc。的(118)
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Studies on the Antimetabolites of Amino Acids. (VIII) : Formation of Arginosuccinic Acid and Canavanosuccinic : Acid in Microorganisms
S Studies on the Antimetabolites of Amino Acids. (VIII) Formation of Arginosuccinic Acid and Canavanosuccinic Acid in Microorganisms Tomoji SUZUKI, Saburo MUPAOKA and Teruo MAKINO (Suzuki Laboratory) Journal of the Pharmaceutical Society of Japan (Yakugaku Zasshi), 77, 282 (1957) Acetone-dried cells of Escherichia coli and Lactobacillus arabinosus were prepared and the formation of arginosuccinic acid (ASA) and canavanosuccinic acid (CSA) from arginine or canavanine and fumarate was followed by paper electrophoresis and paper chromatography. ASA was found to be formed by the parent strain of E. coli but it was not detected with its arginine-requiring mutant (cannot be compensated with ornithine or citrulline). Even with the parent strain, its culture in a medium containing arginine causes disappearance of arginosuccinase activity and ASA formation does not take place. The formation of CSA was identical with the case of ASA. With Lact. arabinosus ASA was formed from citrulline and aspartic acid, as well as from arginine and fumarate. CSA itself inhibits proliferation of Lact. arabinosus and this inhibition is easily recoverd with arginine. Considerations were made on the action mechanism of canavanine from these experimental results. Studies on the Antimetabolites of Amino Acids. (IX) Biological Activity of Aspartic Acid Monoand Dihydrazide Tomoji SUZUKI and Fumihiko TANAKA (Suzuki Laboratory) Journal of the Pharmaceutical Society of Japan (Yakugaku Zasshi), 77, 1218 (1957) As partic acid monoand dihydrazides, and 3-hydroxyaspartic acid were synthesized and their action in inhibiting the growth of Leuconostoc mesenteroides P-60 and Escherichia coli No. 1 was examined. In the presence of aspartic acid, growth of Leuc. mesenteroides was completely inhibited by 100 r/cc. of monohydrazide, 500 r/cc. of 3-hydroxyaspartic acid, and 2000 r/cc. of dihydrazide. So far as Leuc. mesenteroides is concened, therefore, the growthinhibitory action of monohydrazide is stronger than that of dihydrazide. On the contrary, the growth of E. coli No. 1, which requires no aspartic acid for growth, was more strongly inhibited by the dihydrazide, the effective concentration for 50 9 inhibition being 55 r/cc. of the monohydrazide and 33 r/cc. of (118)
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