Kim Young-Hwa, Kim Yunhee, Cho Eunhee, Kwak Sangsoo, Kwon Sukyoon, Bae Jungmyung, Lee Baekrak, Meen Byungin, Huh Gyung-Hye
Genome Research Center, Inje University, 607 Obangdong, Gimhae 621-749, Gyungnam, Republic of Korea.
Phytochemistry. 2004 Sep;65(17):2471-6. doi: 10.1016/j.phytochem.2004.08.001.
Cultured plant cells are a good system for the study of antioxidant mechanisms and for the mass production of antioxidants, because they can be grown under conditions of high oxidative stress. Alterations in the intracellular and extracellular activities of three antioxidant enzymes, superoxide dismutase (SOD), guaiacol-type peroxidase (POD), and glutathione peroxidase (GPX), were investigated in suspension cultures of sweetpotato (Ipomoea batatas) during cell growth. Intracellular SOD activities (units/mg protein) at 15 days after subculture (DAS) and 30 DAS were 10 and 20 times higher, respectively, compared with the SOD activity at 1 DAS, whereas intracellular specific POD and GPX activities did not significantly increase until after 15 DAS, when they rapidly increased. The extracellular activities of the three enzymes in culture medium were much higher than were the intracellular activities. The change in extracellular SOD activity was similar to that of extracellular GPX during cell growth. Those activities showed high levels until 5 DAS and then significantly decreased. Extracellular POD activity had an almost constant level regardless of the cell growth stage. In addition, intracellular SOD and POD isozymes were quite different from those isozymes in the culture medium. The changes in SOD and POD isozymes observed here suggest that different isozymes might modulate the levels of reactive oxygen intermediates during cell growth. Characterization of extracellular antioxidant enzymes discovered here would provide a new understanding for defense mechanism in plants.
培养的植物细胞是研究抗氧化机制和大规模生产抗氧化剂的良好系统,因为它们可以在高氧化应激条件下生长。在甘薯(Ipomoea batatas)悬浮培养物的细胞生长过程中,研究了三种抗氧化酶,即超氧化物歧化酶(SOD)、愈创木酚型过氧化物酶(POD)和谷胱甘肽过氧化物酶(GPX)的细胞内和细胞外活性变化。继代培养15天(DAS)和30 DAS时的细胞内SOD活性(单位/毫克蛋白质)分别比继代培养1 DAS时的SOD活性高10倍和20倍,而细胞内特异性POD和GPX活性直到15 DAS后才显著增加,此后迅速上升。培养基中这三种酶的细胞外活性远高于细胞内活性。细胞生长过程中,细胞外SOD活性的变化与细胞外GPX的变化相似。这些活性在5 DAS之前一直保持在较高水平,然后显著下降。无论细胞生长阶段如何,细胞外POD活性几乎保持恒定。此外,细胞内SOD和POD同工酶与培养基中的同工酶有很大不同。此处观察到的SOD和POD同工酶的变化表明,不同的同工酶可能在细胞生长过程中调节活性氧中间体的水平。此处发现的细胞外抗氧化酶的特性将为植物的防御机制提供新的认识。