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FIRST REVIEW
OF
PROJECT
PRESENTATION
NAME: KALAIVANI B
REG NO:212420214011
DEPARTMENT: BIOTECHNOLOGY
YEAR: FINAL YEAR
COLLEGE: SREE SASTHA INSTITUTE OF
ENGINEERING AND TECHNOLOGY
EXTERNAL GUIDE
Dr.P.GANESAN,
SENIOR SCIENTIST,
DEPARTMENTOF BIOTECHNOLOGY,
CSIR-CLRI.
INTERNAL GUIDE
Ms.JENNIFIER,
ASSISTANT PROFESSOR,
DEPARTMENTOF BIOTECHNOLOGY,
SREE SASTHA INSTITUTE OF
ENGINEERING AND TECHNOLOGY.
TITLE
EXTRACTION, PURIFICATION AND
CHARACTERISTICS OF PHYCOERYTHRIN FROM
GRACILLARIA
AIM:
To extract and purify Phycoerythrin from Gracillaria.
OBJECTIVE:
✓ To isolate Phycoerythrin pigment protein complex from Gracillaria.
✓ To extract and purify the Phycoerythrin complex which is been isolated.
✓ To study the various characteristics of Phycoerythrin.
INTRODUCTION
✓ Light harvesting protein pigmented complex from red algae and cryptophytes.
✓ Any of a group of red photosynthetic pigments present in red algae and some
cyanobacteria.
✓ Used as a fluorescent probe or as a colorant in the food and cosmetic industries.
✓Substantial economic impact due to its potential as a natural food colorant.
R-PE:
•Molecularweight:
✓ 240 to 260 Kda.
✓most abundantin Rhodophytes.
✓ composed of an (αβ)6 γ complex.
•Subunits:
✓ α- 2 phycoerythrobilins(PEB)
✓ β- 2 or 3 PEBs and 1 phycourobilin(PUB)
✓ γ(s)
• Stability:
✓ Good stability towardstemperature, upto 40°C.
✓ At 60°C,the reduction in concentrationof B- Phycoerythrin and R- Phycoerythrin. 50+ 3.4% and
70+ 0.18% respectively.
• Charge
✓ negatively charge.
• pI
✓ 4.89 where pH 4.5 to 6.0net charge will become zero.
Gracillaria Algae Structure of Phycoerythrin
Gracillaria Algae → Wash and freeze at 4°C to 10°C. → Lyophilization process → Grain the algae in the form of powder.
↓
Measuring the weight.
↓
Take upto 5g of grained sample.
↓
Add 0.1 molar of sodium phosphate buffer.
|
Purification. ← Collect the supernatant ← Ultra sonification ← Maceration for 30mins ↲
↓
HPLC
↓
Physio - Chemical Characteristics.
METHODOLOGY
APPLICATION
KALAIVANI B-1.pdf

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KALAIVANI B-1.pdf

  • 2. NAME: KALAIVANI B REG NO:212420214011 DEPARTMENT: BIOTECHNOLOGY YEAR: FINAL YEAR COLLEGE: SREE SASTHA INSTITUTE OF ENGINEERING AND TECHNOLOGY
  • 3. EXTERNAL GUIDE Dr.P.GANESAN, SENIOR SCIENTIST, DEPARTMENTOF BIOTECHNOLOGY, CSIR-CLRI. INTERNAL GUIDE Ms.JENNIFIER, ASSISTANT PROFESSOR, DEPARTMENTOF BIOTECHNOLOGY, SREE SASTHA INSTITUTE OF ENGINEERING AND TECHNOLOGY.
  • 4. TITLE EXTRACTION, PURIFICATION AND CHARACTERISTICS OF PHYCOERYTHRIN FROM GRACILLARIA
  • 5. AIM: To extract and purify Phycoerythrin from Gracillaria. OBJECTIVE: ✓ To isolate Phycoerythrin pigment protein complex from Gracillaria. ✓ To extract and purify the Phycoerythrin complex which is been isolated. ✓ To study the various characteristics of Phycoerythrin.
  • 6. INTRODUCTION ✓ Light harvesting protein pigmented complex from red algae and cryptophytes. ✓ Any of a group of red photosynthetic pigments present in red algae and some cyanobacteria. ✓ Used as a fluorescent probe or as a colorant in the food and cosmetic industries. ✓Substantial economic impact due to its potential as a natural food colorant.
  • 7. R-PE: •Molecularweight: ✓ 240 to 260 Kda. ✓most abundantin Rhodophytes. ✓ composed of an (αβ)6 γ complex. •Subunits: ✓ α- 2 phycoerythrobilins(PEB) ✓ β- 2 or 3 PEBs and 1 phycourobilin(PUB) ✓ γ(s) • Stability: ✓ Good stability towardstemperature, upto 40°C. ✓ At 60°C,the reduction in concentrationof B- Phycoerythrin and R- Phycoerythrin. 50+ 3.4% and 70+ 0.18% respectively. • Charge ✓ negatively charge. • pI ✓ 4.89 where pH 4.5 to 6.0net charge will become zero.
  • 8. Gracillaria Algae Structure of Phycoerythrin
  • 9. Gracillaria Algae → Wash and freeze at 4°C to 10°C. → Lyophilization process → Grain the algae in the form of powder. ↓ Measuring the weight. ↓ Take upto 5g of grained sample. ↓ Add 0.1 molar of sodium phosphate buffer. | Purification. ← Collect the supernatant ← Ultra sonification ← Maceration for 30mins ↲ ↓ HPLC ↓ Physio - Chemical Characteristics. METHODOLOGY