Induced Defense Related Enzyme Activities of Tomato Plant by Indigenous Endophytic Bacteria and Challenged by Ralstonia Syzigii Subsp. Indonesiensis

Y. Yanti, W. Warnita, R. Reflin
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引用次数: 1

Abstract

Our previous research had screened 9 best indigenous endophytic isolates for their ability to control Ralstonia syzigii subsp. indonesiensis, the causal agents of bacterial wilt disease in tomato ( Lycopersicon esculentum ) in green house condition. Those 9 strains were B acillus cereus EPL1.1.3 , B. cereus TLE2.3, B. toyonensis EPL1.1.4 , Serratia nematodiphila TLE1.1, B. anthracis SNE2.2, B. cereus E1.AB1.2, B. cereus E1AB2.1, Enterobacter cloacae subsp. dissolvens TLE2.2 and S. marcescens KLE3.3. The purposed of this study is to test the ability of the endophytic bacteria strains in increasing defense related enzyme activities of tomato. Bacterial strains were tested for its ability to induce the defense-related enzymes which were phenylalanine ammonia lyase (PAL), peroxidase (PO) and polyphenol oxidase (PPO) in roots and leaves of tomato plants. R. syzigii subsp. indonesiensis inoculated to host plants 7 days after the endophyte bacteria strains inoculation. Enzyme activities were recorded at 0, 1, 3, 5, 7, 9, 12 and 15 days after pathogen inoculation (dpi).  It was observed that PAL, PO and PPO activities were significantly increased in all of the endophytic bacteria inoculated treatments compared to control plant. Activities of PAL in the leaves was fast similar to the roots; but PO activities was higher in the roots compared to that in the leaves, whereas PPO activities was higher in the leaves than in the roots. PAL and PO reached the maximum level at different time in the leaves (3 dpi and 15 dpi), in the roots (5 dpi and 12 dpi), whereas PPO in the leaves at 12 dpi and in the roots at 9 dpi.
本地内生细菌对番茄植株防御相关酶活性的诱导及syziralstonia亚种的攻毒Indonesiensis
我们在前期的研究中筛选出了9株具有较好控制syzigii亚种的本土内生菌株。温室条件下番茄青枯病病原菌印尼氏菌的研究。9株菌株分别为蜡样芽孢杆菌EPL1.1.3、蜡样芽孢杆菌TLE2.3、托约氏芽孢杆菌EPL1.1.4、嗜线虫沙雷菌TLE1.1、炭疽芽孢杆菌SNE2.2、蜡样芽孢杆菌E1.AB1.2、蜡样芽孢杆菌E1AB2.1、阴沟肠杆菌亚种。溶出TLE2.2和粘多糖KLE3.3。本研究的目的是测试内生细菌菌株提高番茄防御相关酶活性的能力。研究了菌株对番茄根系和叶片中苯丙氨酸解氨酶(PAL)、过氧化物酶(PO)和多酚氧化酶(PPO)等防御相关酶的诱导能力。syzigii亚种内生菌菌株接种后7天接种到寄主植株上。分别于病原菌接种后0、1、3、5、7、9、12和15 d记录酶活性。结果表明,与对照植株相比,接种各内生细菌的PAL、PO和PPO活性均显著提高。PAL在叶片中的活性与根相似;但根中PPO活性高于叶,而叶中PPO活性高于根。PAL和PO在叶片(3 dpi和15 dpi)和根系(5 dpi和12 dpi)中均在不同时间达到最大值,而PPO在叶片(12 dpi)和根系(9 dpi)中均达到最大值。
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