Ohta S, Usami S, Ueki J, Kumashiro T, Komari T, Burnell J N
Plant Breeding and Genetics Research Laboratory, Japan Tobacco Inc., Iwata, Shizuoka, Japan.
FEBS Lett. 1996 Nov 4;396(2-3):152-6. doi: 10.1016/0014-5793(96)01084-8.
Pyruvate,orthophosphate dikinase (PPDK), an enzyme important in C4 photosynthesis, is typically a cold-sensitive enzyme. However, a cold-tolerant form of the enzyme has been isolated from the leaves of Flaveria brownii. Using an Escherichia coli expression system and the PPDK cDNAs from F. brownii (cold-tolerant), F. bidentis (cold-sensitive) and maize (intermediate cold tolerance), site-directed mutagenesis studies indicated that as few as three amino acids residues (of 880 residues) strongly influence the cold sensitivity of Flaveria PPDK. Gel filtration analysis of the PPDK expressed in E. coli showed that subunit association and cold tolerance are closely linked.
丙酮酸,磷酸双激酶(PPDK)是一种在C4光合作用中起重要作用的酶,通常是一种对冷敏感的酶。然而,已从布朗黄菊的叶片中分离出该酶的一种耐冷形式。利用大肠杆菌表达系统以及来自布朗黄菊(耐冷)、二齿黄菊(冷敏感)和玉米(中等耐冷性)的PPDK cDNA进行定点诱变研究表明,在880个氨基酸残基中,仅有三个氨基酸残基强烈影响黄菊PPDK的冷敏感性。对在大肠杆菌中表达的PPDK进行凝胶过滤分析表明,亚基缔合与耐冷性密切相关。