Department of Vegetable Crops, University of California, Davis, California 95616.
Plant Physiol. 1986 Jun;81(2):637-41. doi: 10.1104/pp.81.2.637.
Since 1-(malonylamino)cyclopropane-1-carboxylic acid (MACC), the major conjugate of 1-aminocyclopropane-1-carboxylic acid (ACC) in plant tissues, is a poor ethylene producer, it is generally thought that MACC is a biologically inactive end product of ACC. In the present study we have shown that the capability of watercress (Nasturtium officinale R. Br) stem sections and tobacco (Nicotiana tabacum L.) leaf discs to convert exogenously applied MACC to ACC increased with increasing MACC concentrations (0.2-5 millimolar) and duration (4-48 hours) of the treatment. The MACC-induced ethylene production was inhibited by CoCl(2) but not by aminoethoxyvinylglycin, suggesting that the ACC formed is derived from the MACC applied, and not from the methionine pathway. This was further confirmed by the observation that radioactive MACC released radioactive ACC and ethylene. A cell-free extract, which catalyzes the conversion of MACC to ACC, was prepared from watercress stems which were preincubated with 1 millimolar MACC for 24 hours. Neither fresh tissues nor aged tissues incubated without external MACC exhibited enzymic activity, confirming the view that the enzyme is induced by MACC. The enzyme had a K(m) of 0.45 millimolar for MACC and showed maximal activity at pH 8.0 in the presence of 1 millimolar MnSO(4). The present study indicates that high MACC levels in the plant tissue can induce to some extent the capability to convert MACC to ACC.
由于 1-(丙二酰氨基)环丙烷-1-羧酸(MACC)是植物组织中 1-氨基环丙烷-1-羧酸(ACC)的主要轭合物,它是一种较差的乙烯产生物,因此通常认为 MACC 是 ACC 的生物上无活性的终产物。在本研究中,我们已经表明,豆瓣菜(Nasturtium officinale R. Br)茎段和烟草(Nicotiana tabacum L.)叶圆片将外源施加的 MACC 转化为 ACC 的能力随着 MACC 浓度(0.2-5 毫摩尔)和处理时间(4-48 小时)的增加而增加。MACC 诱导的乙烯产生被 CoCl2 抑制,但不受氨基乙氧基乙烯基甘氨酸的抑制,这表明形成的 ACC 源自施加的 MACC,而不是源自蛋氨酸途径。这进一步通过观察到放射性 MACC 释放放射性 ACC 和乙烯得到证实。从预先用 1 毫摩尔 MACC 孵育 24 小时的豆瓣菜茎制备了一种无细胞提取物,该提取物催化 MACC 向 ACC 的转化。新鲜组织和未孵育外部 MACC 的老化组织均未表现出酶活性,这证实了该酶被 MACC 诱导的观点。该酶对 MACC 的 K(m)为 0.45 毫摩尔,在存在 1 毫摩尔 MnSO4 时在 pH 8.0 下表现出最大活性。本研究表明,植物组织中高浓度的 MACC 可以在一定程度上诱导将 MACC 转化为 ACC 的能力。