Skip to main content

Generalized Life Cycle of Basidiomycota-Plant Care

Generalized Life Cycle of Basidiomycota-Plant Care

GENERALIZED LIFE CYCLE OF BASIDIOMYCOTA
Basidiomycota is one of two large phyla that, together with the Ascomycota, comprise the subkingdom Dikarya (often referred to as the "higher fungi") within the kingdom Fungi. Basically, Basidiomycota are filamentous fungi composed of hyphae (except for yeasts), and reproducing sexually via the formation of specialized club- shaped end cells called basidia that normally bear external meiospores (usually four). These specialized spores are called basidiospores.
(Edited from Google images).
------------------------------------------------------------------------------------------
Here You Can Find Plant Disease and Pathogens (Fungi, Bacteria, Molllicutes, Parasitic higher plants, Parasitic Green Algae, Nematodes, Protozoa, Viruses, Viroids,Prions) Diagnosis and Treatment, Control Against Plant Disease. Laboratory Experiments & Work. Plant Pathology Lab Manual. House Plant-Trees Care Guide, Snake Plant Care, Pothos Plant Care, Plant Care for dummies, Plant Care  Printable, Products, Plant Care Tips, Symbols, Tags, Database, Careers, Websites, Apps & Card.
Written By:
Dr.Qaiser Shakeel
Tahir Mahmood
Department of Plant Pathology-Agriculture
The Islamia University of Bahwalpur-Pakistan.

Comments

Popular posts from this blog

Preparation of Media For Culture-PDA, PDB & NA Recipes

PREPARATION OF MEDIA FOR CULTURE: Media play an important role not only for the nutrition and growth of the pathogen but also in identification through growth pattern on media. Fungi and Bacteria need synthetic media enriched with essential element for the growth. In general different types of media are prepared to culture fungi and bacteria but Potato dextrose agar (PDA) for fungi and Nutrient agar for bacteria are being used commonly.  RECIPES OF DIFFERENT MEDIA: POTATO DEXTROSE AGAR: Potato Starch 250  mL/15g Dextrose-15g Agar -Agar 15g Distilled water  750 mL/1000mL PROCEDURE TO PREPARE POTATO DEXTROSE AGAR MATERIAL: Petri dish, Flask, test tubes, Agar-agar, Dextrose, Potato starch, Water PROCEDURE: First of all take potatoes to extract potato starch. Peel the potatoes and cut into small pieces. Preferably 200 g of potato pieces are weighed, washed quickly in running water, placed in 1l liter of water and boil...

Media Recipes For Pathogens (Bacterial) Growth On Artificial Mediums

Media Recipes For Pathogens Growth On Artificial Mediums CPG (1L) CPG (For One Litter Solution) Differential media for Ralstonia from laboratory guide for identification of Plant Pathogenic Bacteria 1.0g      Casamino acid (casein hydrolysate) 10.0g    Peptone 5.0g      Glucose 17.0g    Agar Media Recipes For Pathogens Growth On Artificial Mediums YNA (Yeast extract nutrient agar) - (For 1L) Differential media for Xanthamonas from laboratory guide for identification of Plant Pathogenic Bacteria 5.0g     Yeast extract 23.0g   Nutrient agar NA (Nutrient agar) (1L) Media Recipes For Pathogens Growth On Artificial Mediums Cultivation of a wide variety of Microorganisms from Difco Nutrient Agar container 23.0g      Nutrient Agar 1/4 PDA (QPDA) (Potato Dextrose Agar) (1L) 9.75g   Potato Dextrose Agar 11.25g  Agar PDA (Potato Dextrose Agar) (1L)...

GEL Procedure Of Gel Electrophoresis For Separation DNA/RNA

GEL Procedure Of Gel Electrophoresis For Separation-DNA/RNA GEL ELECTROPHORESIS GEL Procedure Of Gel Electrophoresis For Separation-DNA/RNA Mix 1 g agarose in 99mL of TAE/TBE buffer and heat it in the oven. Add 10 uL of 10mg/mL ethidium bromide in 100 mL of hand cold agarose gel solution. Pour this mixture into gel caster/tray having comb and sealed from sides. Let it be solidified at room temperature for 30-60 minutes. Remove the comb seals from the gel caster and place it inside the gel tank containing TAE/TBE buffer. Put the DNA samples/PCR product (mixed in 6x loading dye) inside each well and note it in the lab. Notebook. Attach the cathode (towards wells) end of gel and anode (at the bottom) of the power supply to the gel tank. Switch on the power supply giving 80-120 volts and run it for sufficient time allowing the samples to travel in more than half of the gel length. Take the gel out of the gel tank and observe it in a gel doc system/UV transillumin...