Department of Botany, University of Wisconsin, Madison, Wisconsin 53706.
Plant Physiol. 1992 Sep;100(1):210-5. doi: 10.1104/pp.100.1.210.
Oxygen sensitivity and partitioning of carbon was measured in a mutant line of Flaveria linearis that lacks most of the cytosolic fructose-1,6-bisphosphatase found in wild-type lines. Photosynthesis of leaves of the mutant line was nearly insensitive to O(2), as found before. The mutant plants partitioned 2.5 times less carbon into sucrose than the wild type in a pulse chase experiment, with the extra carbon going mainly to starch but also to amino acids. From 10 to 50 min postlabeling, radioactivity chased out of the amino acid fraction to starch in both lines. In the middle of the light period, starch grains were larger in the mutant than in the wild type and covered 30% of the chloroplast area as seen with an electron microscope. Starch grains were found in both mesophyll and bundle sheath chloroplasts in both lines in these C(3)-C(4) intermediate plants. At the end of the dark period, the starch levels were considerably reduced from what they were in the middle of the light in both lines. The concentration of sucrose was higher in the mutant line despite the lack of cytosolic fructose-1,6-bisphosphatase. The amino acid fraction accounted for about 30% of all label following a 10-min chase period. In the mutant line, most of the label was in the glycine + serine fraction, with 10% in the alanine fraction. In wild-type leaves, 35% of the label in amino acids was in alanine. These results indicate that this mutant survives the reduced cytosolic fructose-1,6-bisphosphatase activity by partitioning more carbon to starch and less to sucrose during the day and remobilizing the excess starch at night. However, these results raise two other questions about this mutant. First, why is the sucrose concentration high in a plant that partitions less carbon to sucrose, and second, why is alanine heavily labeled in the wild-type plants but not in the mutant plants?
氧敏感性和碳的分配在 Flaveria linearis 的突变体中进行了测量,该突变体缺乏野生型中发现的大多数细胞质果糖-1,6-二磷酸酶。与以前一样,突变体叶片的光合作用对 O(2)几乎不敏感。在脉冲追踪实验中,突变体植物将 2.5 倍的碳分配到蔗糖中,而野生型植物则将更多的碳分配到淀粉中,但也分配到氨基酸中。在标记后 10 到 50 分钟,放射性物质从两种类型的氨基酸部分追踪到淀粉。在光周期的中间,突变体中的淀粉粒比野生型中的淀粉粒大,并且在电子显微镜下观察到淀粉粒覆盖叶绿体区域的 30%。在这些 C(3)-C(4)中间植物中,在两种类型的叶片中都发现了质体和束鞘质体中的淀粉粒。在黑暗期结束时,两种类型的淀粉水平都从光周期中间的水平大大降低。尽管缺乏细胞质果糖-1,6-二磷酸酶,突变体中的蔗糖浓度仍然较高。在 10 分钟的追踪期后,氨基酸部分占所有标记物的约 30%。在突变体中,大部分标记物在甘氨酸+丝氨酸部分,丙氨酸部分占 10%。在野生型叶片中,氨基酸中 35%的标记物是丙氨酸。这些结果表明,这种突变体通过在白天将更多的碳分配到淀粉中而不是蔗糖中,并且在夜间重新利用多余的淀粉来维持细胞质果糖-1,6-二磷酸酶活性降低。然而,这些结果提出了关于该突变体的另外两个问题。首先,为什么在将较少的碳分配到蔗糖的植物中蔗糖浓度较高,其次,为什么在野生型植物中丙氨酸被大量标记而在突变体植物中没有被标记?