首页> 外国专利> STANDARDIZATION OF ISOLATION TECHNIQUES FOR CEPHALEUROS PARASITICUS KARST, A PATHOGENIC ALGA IN TEA PLANTS

STANDARDIZATION OF ISOLATION TECHNIQUES FOR CEPHALEUROS PARASITICUS KARST, A PATHOGENIC ALGA IN TEA PLANTS

机译:茶树病原性海藻寄生头孢虫的分离技术的标准化

摘要

Among the leaf diseases in tea plants, red rust caused by a pathogenic alga Cephaleuros parasiticus Karst is found to be very important and more serious in tea plantations. Although the disease is known for over 40 years in all the tea growing countries, the disease has become a major problem only in recent years on the estates now resort to large scale replanting, infilling and inter row planting to increase production and productivity. No efforts are being made so far to isolate and study the culture characteristics of the alga under in vitro condition. It is in. this scenario the present investigation has been proposed to isolate the pathogen from infected leaf maierials The infected leaves will be washed with Tween 20 and surface sterilized using (15%) Mercuric chloride solution followed by repeated washing with sterile distilled water. The infected portion is cut into small pieces using sterile scissors and transferred to the culture vials containing Bristol medium, fhe culture vials are maintained at a temperature of 25±2°C under built in white fluorescent light at a photon flux density of 30-50 µEm2"S-2 with a photoperiodic regime of 16 hrs light and 8 hrs dark cycles. The promiment algal filaments emerging from infected portion will be transferred to fresh algal broth as well as on solid medium for further grcnvth. The present study mav be useful to develop an easy, reliable and reproducible technique for culturing this alga. Moreover, it will also be useful to study the culture characteristic features, life cycle and genetic diversity of C parasiticus, besides to screen various fungicides and biocontrol agents to control the pathogen very effectively under in situ.
机译:在茶树的叶片疾病中,由致病性藻寄生头孢(Cephalleuros parasiticus Karst)引起的红锈在茶园中非常重要且更为严重。尽管这种病在所有茶叶种植国中已经有40多年的历史了,但直到最近几年,这种病才成为一个主要问题,因为现在这些酒庄开始大规模种植,填充和行间种植以提高产量和生产力。迄今为止,尚未做出任何努力来分离和研究体外条件下藻类的培养特性。在这种情况下,已提出本研究以从感染的叶片材料中分离病原体。感染的叶片将用Tween 20洗涤,并用(15%)氯化汞溶液进行表面消毒,然后用无菌蒸馏水重复洗涤。用无菌剪刀将被感染的部分切成小块,并转移到含有Bristol培养基的培养瓶中,将培养瓶在内置荧光灯下以25-50的光子通量密度保持在25±2°C的温度下µEm2“ S-2的光照周期为16小时光照和8小时黑暗周期。从受感染部位出来的优质藻丝将被转移到新鲜的藻肉汤中以及固体培养基上以进一步生长。本研究可能是有用的开发一种简便,可靠和可重复的藻类培养技术,除了筛选各种杀菌剂和生物防治剂以控制病原菌外,研究C寄生虫的培养特征,生命周期和遗传多样性也将非常有用。有效地在原地。

著录项

  • 公开/公告号IN2009CH01997A

    专利类型

  • 公开/公告日2009-10-30

    原文格式PDF

  • 申请/专利权人

    申请/专利号IN1997/CHE/2009

  • 发明设计人 DR P PONMURUGAN;

    申请日2009-08-21

  • 分类号C12P19/00;

  • 国家 IN

  • 入库时间 2022-08-21 19:27:00

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