Iwanaga M, Kuyyakanond T
Department of Bacteriology, School of Medicine, University of the Ryukyus, Okinawa, Japan.
J Clin Microbiol. 1987 Dec;25(12):2314-6. doi: 10.1128/jcm.25.12.2314-2316.1987.
A large amount of cholera toxin (CT) was produced by Vibrio cholerae O1 cultured in yeast extract-peptone water. The organisms were cultured initially in a stationary test tube (small surface-to-volume ratio) until the end of the exponential phase and subsequently cultured in a shaking flask for 15 to 20 h. By this method (previously reported as the AKI-SW method), most cholera vibrios produced an abundance of CT (up to 64 micrograms/ml), regardless of their biotype and serotype. A substantial amount of CT was produced even in basic peptone water (2% peptone, 0.5% NaCl). Use of sodium bicarbonate, which markedly stimulated CT production in the stationary test tube culture, was undesirable for CT production by the culture method used here. CT production was greatly influenced by culture conditions but was not significantly affected by the composition of the medium.
在酵母提取物蛋白胨水中培养的霍乱弧菌O1产生了大量霍乱毒素(CT)。这些微生物最初在静止的试管中培养(表面积与体积比小),直到指数生长期结束,随后在摇瓶中培养15至20小时。通过这种方法(先前报道为AKI-SW方法),大多数霍乱弧菌产生大量CT(高达64微克/毫升),无论其生物型和血清型如何。即使在基本蛋白胨水(2%蛋白胨,0.5%氯化钠)中也产生了大量CT。使用碳酸氢钠在静止试管培养中能显著刺激CT产生,但对于此处所用的培养方法而言,并不利于CT的产生。CT的产生受培养条件的极大影响,但不受培养基成分的显著影响。