Wemmer T, Kaufmann H, Kirch H H, Schneider K, Lottspeich F, Thompson R D
Max-Planck-Institut für Züchtungsforschung, Köln, Germany.
Planta. 1994;194(2):264-73.
An abundant, pistil-specific basic protein has been purified and characterized from potato (Solanum tuberosum L.). A polymerase chain reaction (PCR) probe was generated for the corresponding gene using oligonucleotides based on internal peptide sequences of the protein, and the PCR probe was further employed to isolate cDNA and genomic clones. The sequence of the gene exhibits up to 70% similarity to previously described endochitinase class 1a protein sequences, and the purified protein possesses chitinase (poly[1, 4-(N-acetyl-beta-D-glucosaminide)] glucanohydrolase, EC 3.2.1.14) activity. The protein, termed SK2, has been located by immunocytochemistry to the intercellular matrix of the stylar transmitting tract. Immunoblot analysis has shown SK2 to be distinct from the wound-induced chitinases of potato. The SK2-class of chitinase is restricted in its distribution within the Solanaceae to the sub-family Solanoidae, which includes cultivated tomato and potato species. It was absent from the Cestroidae species tested (Petunia hybrida, Nicotiana tabacum). A role for SK2 endochitinase in protecting the ovary against pollen-tube-mediated pathogen ingress is proposed.
从马铃薯(Solanum tuberosum L.)中纯化并鉴定了一种丰富的、雌蕊特异性碱性蛋白。利用基于该蛋白内部肽序列的寡核苷酸为相应基因生成了聚合酶链反应(PCR)探针,并进一步用该PCR探针分离cDNA和基因组克隆。该基因的序列与先前描述的1a类内切几丁质酶蛋白序列具有高达70%的相似性,纯化后的蛋白具有几丁质酶(聚[1,4-(N-乙酰-β-D-氨基葡糖苷)]葡聚糖水解酶,EC 3.2.1.14)活性。这种名为SK2的蛋白通过免疫细胞化学定位在花柱传递组织的细胞间基质中。免疫印迹分析表明SK2与马铃薯伤口诱导的几丁质酶不同。SK2类几丁质酶在茄科中的分布仅限于茄亚科,其中包括栽培番茄和马铃薯品种。在所测试的夜香树科物种(矮牵牛、烟草)中不存在。有人提出SK2内切几丁质酶在保护子房免受花粉管介导的病原体侵入方面发挥作用。