Internship Report: Nivedha A (192BT145)
Internship Report: Nivedha A (192BT145)
Internship Report: Nivedha A (192BT145)
INTERNSHIP REPORT
Submitted by
NIVEDHA A
(192BT145)
Internship
at
BIOTECHNOLOGY
APRIL-2022
ABSTRACT:
INTRODUCTION:
Upstream Bioprocessing
of product for desired quality. When it reaches batch and fed batch
bioprocess.
Downstream Bioprocessing
cell mass from the upstream are processed to meet purity and quality
processing are
Separation of biomass
Cell disruption
Concentration of broth
Dewatering
Polishing of metabolites
INTRODUCTION OF THE COMPANY:
Product details:
Biofertilizer:
Biopesticides:
Biopesticides are a vital component of sustainable agriculture. Biopesticides are
derived from natural materials such as animals, plants, bacteria, and certain
minerals widely used for controlling insects and disease causing pathogens.
Insecticides:
Insecticide are sprayed on the plant when the insects starts consuming any part
of the plant the insect dies.
Nematicide:
The nematicides are use to kill nematodes in their larval stage the nematicide
containing organisms are mixed with soil or fertilizer or compost and when the
plant gets the nematicide the organisms grow on the larva and kills the
nematodes.
• Poultry
• Aquvaculture
• Animal health
PRODUCTS CAN BE OFFERED AS
Talc/ Granular/ liquid-based products
Freeze dried products
Thermostable microencapsulated products
Technics learnt:
For 300ml
Peptone –1.5g
Beef extract – 0.9g
Nacl – 1.5g
Agar –3.75g
To adjust pH, NaOH is used - 1N in 100ml
Bacterial straining:
The Gram stain involves staining bacteria, fixing the color with a mordant,
decolorizing the cells, and applying a counterstain.
• Take bacterial sample 20µl water mount it and smear it well, and heat fix for
1 minute.
• Add few drops of crystal violet and leave it for 1 minute.
• Rince it with water.
Fungal staining:
QC protocols:
• Shake the flask vigorously and transfer 1 ml / 1000 µl of the aliquot from the
flask to 9ml sterile water blank in a test tube with a 1000 µl Micropipette to get
10²dilution.
(Note: If Micropipette is used, change the tips for every transfer of the diluents).
(Note: Mix the contents of the test tube by using a Vortex Mixer for few
minutes) ..
• Take 0.1 ml/100 µl from alternate dilution tubes viz., 102, 104, 106, 108, 10-
10, 10-12 and transfer to the Petri plates previously plated with Potato Dextrose
Agar.
• Spread it on the agar surface by swirling it with an L rod and label them from
10 to 10¹¹2
correspondingly. Incubate all the plates at room temperature for 5 to 7 days. .
• After the incubation period, count the no. of colonies with typical colony
characters of the fungal bio-control agent being enumerated and work out the
average no. of colonies/plate for each dilution.
(Note: Only use the dilution with the number of colonies ranging between 20-
100 as more colonies per plate may result in reciprocal inhibition).
QC SETUP FLOW DIAGRAM
QC RESULTS
SPREAD PLATE
108 X 10 6 108 X 106
For 10 , Total Population Count = 0.1 =
-6
10−1
= 1.08 X 109
POUR PLATE
For 10-6, Total Population Count = 108 X 10-6
= 1.08 X 10-8