Thimann Laboratories, University of California, Santa Cruz, California 95064.
Plant Physiol. 1975 Feb;55(2):258-64. doi: 10.1104/pp.55.2.258.
The ontogeny of glyoxysomes and leaf peroxisomes has been examined in the cotyledons of germinating watermelon (Citrullus vulgaris) seedlings. Organelles from the cotyledons were extracted by razor blade homogenization and microbodies were separated by sucrose density gradient fractionation. Both kinds of microbodies have the same mean equilibrium density on sucrose gradients.The development of leaf peroxisomes was examined in seedlings transferred to light at 4 days and 10 to 12 days. In seedlings maintained in darkness to the age of 10 to 12 days, glyoxysomal enzymes virtually disappeared, and the losses were paralleled by a corresponding loss in microbody protein. During this period peroxisomal activity was low and changed only slightly. On transfer to light at this stage, the activity of peroxisomal enzymes rose strikingly. The residual glyoxysomal activity disappeared completely, and the developmental pattern of microbody catalase and microbody protein paralleled the light-induced glyoxysomal disappearance.Similar patterns of microbody development were observed when 4-day-old dark-grown seedlings with maximum glyoxysomal activities were exposed to light. The activity of the peroxisomal enzymes increased and the glyoxysomal enzymes disappeared at a faster rate than in darkness. These changes were again paralleled by the accelerated demise of microbody catalase and microbody protein. Thus under both conditions glyoxysomes were selectively destroyed during peroxisomal development, and the amount of peroxisomes produced was insufficient to offset the loss of glyoxysomal protein. The results do not support the contention that glyoxysomes are transformed to leaf peroxisomes in developing cucurbit cotyledons and favor the view that the two kinds of microbody arise independently of each other.
已在发芽西瓜(Citrullus vulgaris)幼苗的子叶中检查了乙醛酸体和叶过氧化物酶体的个体发生。通过剃刀片匀浆提取子叶中的细胞器,并通过蔗糖密度梯度分级分离微体。这两种微体在蔗糖梯度上具有相同的平均平衡密度。在第 4 天和第 10 至 12 天将幼苗转移到光照下时,检查了叶过氧化物酶体的发育。在将子叶保持在黑暗中至 10 至 12 天的年龄的幼苗中,乙醛酸体酶几乎消失,并且微体蛋白的损失与相应的损失相平行。在此期间,过氧化物酶体活性较低,变化很小。在该阶段转移到光照下时,过氧化物酶体酶的活性急剧上升。残留的乙醛酸体活性完全消失,并且微体过氧化氢酶和微体蛋白的发育模式与光诱导的乙醛酸体消失相平行。当具有最大乙醛酸体活性的 4 天大的黑暗生长幼苗暴露于光下时,观察到类似的微体发育模式。过氧化物酶体酶的活性增加,并且乙醛酸体酶的消失速度比在黑暗中更快。这些变化再次与微体过氧化氢酶和微体蛋白的加速消失相平行。因此,在这两种条件下,乙醛酸体在过氧化物酶体发育过程中均被选择性破坏,并且产生的过氧化物体数量不足以抵消乙醛酸体蛋白的损失。结果不支持乙醛酸体在发育中的葫芦科子叶中转化为叶过氧化物酶体的观点,而是支持这两种微体彼此独立产生的观点。