[Intercellular 27 kD protein is a chitinase induced by water stress or Pseudoperonospora cubensis in cucumber leaves].

植物生理与分子生物学学报 Pub Date : 2007-12-01
Peng Chen, Yu-Hong Li, Zhi-Hui Cheng, Tao Chen
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Abstract

Cucumber seedlings were drought-stressed or inoculated with Pseudoperonospora cubensis. After 3 or 6 d the intercellular fluids of treated cucumber leaves were extracted and analyzed. Protein contents increased after pathogen inoculation and a 27-kD protein was found in intercellular fluids (Figs.1, 7). Both 27 kD proteins were purified from the intercellular fluids of cucumber leaves after drought stress or pathogen inoculation by SDS-PAGE and electro-elution protocol respectively (Fig.2, 3). Purified proteins from drought-stressed and P. cubensis infected seedlings were analyzed by MALDI-TOF MS and their peptide mass fingerprinting (PMF) results were obtained (Figs.4, 5). The PMF results were compared with protein database using the software Profound. The results show that the 27 kD proteins from seedlings after drought stress and after P. cubensis infection were the same protein, i.e. an acidic chitinase (Tables 1, 2; Fig.6). The activities of chitinase in the intercellular fluids of cucumber leaves after pathogen inoculation and in those drought stress were also analyzed. Results showed that both treatments induced the increase in chitinase activity (Fig.8), which indicated that chitinase may be involved in the protection of cucumber plant against both pathogen attack and water stress.

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[细胞间27 kD蛋白是水分胁迫或黄瓜假柄孢子虫诱导的几丁质酶]。
对黄瓜幼苗进行干旱胁迫或接种cubensis。处理3 d或6 d后提取黄瓜叶片细胞间液进行分析。接种病原体后,蛋白质含量增加,细胞间液中发现27-kD蛋白(图1、7)。分别用SDS-PAGE和电洗脱技术从干旱胁迫和接种病原体后的黄瓜叶片细胞间液中纯化出27-kD蛋白(图2、3)。利用MALDI-TOF质谱分析干旱胁迫和黄瓜感染幼苗的纯化蛋白,获得其肽质量指纹图谱(PMF)结果(图4、7)。5)利用Profound软件将PMF结果与蛋白质数据库进行比较。结果表明,干旱胁迫后的幼苗27 kD蛋白与受干旱胁迫后的幼苗27 kD蛋白相同,均为酸性几丁质酶(表1、2;图7)。并对黄瓜叶片接种病原菌后细胞间液中几丁质酶的活性和干旱胁迫下的几丁质酶活性进行了分析。结果表明,两种处理均诱导几丁质酶活性升高(图8),表明几丁质酶可能参与了黄瓜植株抵御病原菌侵袭和水分胁迫的保护。
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