PRODUKSI ENSIM KARBOKSI METIL SELULASE DAN EKSO-POLIGALAKTURONASE SERTA PERANANNYA DALAM MENENTUKAN TINGKAT PATOGENSITAS

Karden Mulya, Heni Heni, S. Supriadi, E. M. Adhi
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Abstract

Carboxy methyl selulase and exo-polygalacturonase enzymes production and their role in determining the pathogenicity of Ralstonia solanacearum isolated from gingerBacterial wilt disease on ginger (Zingiber oicinale Roscoe) caused by Ralstonia solanacearum is the most destructive disease Infected tissues show macerated symptom on infected hosts indicating that the pathogen produces plant digestive enzymes. This research was aimed at analizing carboxymethylccllulasc (CMC-ase) and exopolygalacturonase (cxo-PG) enzymes production by the pathogen. In vitro production of CMC-ase of both virulent and avirulcnt isolates of R solanacearum was measured from diameter of clearing zone around bacterial colony on CMC medium whereas exo-PG was measured by the reduction of Na- polygalacturonatc by filtrate of the pathogen culture. Virulence of the pathogen was tested on tomato cultivar Gondol Hijau by pouring 50 ml of pathogen suspension (I07 cfu/ml) around roots of the plant and it was also tested on ginger cultivar Jahe Putih Besar by pricking suspension of pathogen into rhizome and basal pscudostcm of the plant. The results showed that CMC-ase and and PG-asc were produced by virulent isolates of R. solanacearum al 2.23 cm clear zone and 0.662 mg eq. glucose/ml/hour/ODiti, respectively. The avirulent isolates, however. correlated with disease intensity of the isolates. Disease intensity of the virulent isolates was 0.6 and 0.96 on tomato and on ginger plants respectively, whereas the avirulent isolates was 0.04 and 0.00 respectively. Therefore, CMC-ase and exo-PG are important in determining pathogenicity level of/?, solanacearum.
生产ENSIM KARBOKSI甲基SELULASE EKSO-POLIGALAKTURONASE和确定PATOGENSITAS水平中的作用
生姜青枯病(Zingiber oicinale Roscoe)是由青枯病菌引起的最具破坏性的疾病,侵染的组织在被侵染的寄主身上表现出浸湿症状,表明病原菌产生植物消化酶。本研究旨在分析该病原菌产生的羧甲基纤维素酶(CMC-ase)和外聚半乳糖醛酸酶(cxo-PG)酶。用CMC培养基上菌落周围清除带的直径来测定强毒株和无毒株体外CMC酶的产量,用病原菌培养滤液还原聚半乳糖醛酸钠来测定外显子pg的产量。将病原菌悬浮液50 ml (I07 cfu/ml)浸泡在番茄Gondol Hijau根部,检测病原菌的毒力;将病原菌悬浮液刺入生姜Jahe Putih Besar根部和根茎,检测病原菌的毒力。结果表明,番茄红霉毒力强的分离株产CMC-ase和PG-asc,分别为2.23 cm clear zone和0.662 mg eq. glucose/ml/hour/ODiti。然而,无毒的分离株。与分离株的疾病强度相关。毒力菌株对番茄和生姜的致病强度分别为0.6和0.96,而无毒菌株对植株的致病强度分别为0.04和0.00。因此,CMC-ase和exo-PG在确定/?, solanacearum。
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