"Development of microbial treatment of ret liquor generated in a coir ...

More documents

Recommendations

Info

plates were examined for halozones around the colonies indicating the total utilization oftannic acid as carbon and energy source. 2.2.7.b CelIulolysis Cellulolytic potential ofthe segregated cultures were tested in mineral base medium supplemented with filter papers. The mineral base medium having the composition as detailed under section 2.2.3. was dispensed in test tubes at 10ml aliquots and weighed strips of filter papers, one set of Whatman No.1 and another set of ordinary filter paper, were introduced in such a way that 0.5cm of filter paper was projecting out of the medium. The tubes were autoclaved at 10 Ibs for IOmin and inoculated from a nutrient agar grown young culture (24 hour growth). The inoculated tubes were incubated at 28±OAoC for 10 days. Whenever evaporation and subsequent lowering of the level of medium was observed the loss of water was compensated by adding distilled water. Uninoculated controls were also run along with the test. On completion of 10 days incubation the tubes were observed for visible degradation of the filter paper, loss of weight and reducing sugar 22
Page 1 and 2: DEVELOPMENT OF MICROBIAL TREATMENT
Page 5 and 6: ACKNOWLEDGEMENTS I sincerely dedica
Page 7: I also thank all my colleagues Mr.T
Page 10 and 11: 2.3. RESULTS AND DISCUSSIONS 37 2.3
Page 12: CHAPTER -1 GENERAL INTRODUCTION
Page 15 and 16: 'mallis' and dumped in water. Rocky
Page 17 and 18: activity has been attributed to bac
Page 19 and 20: habitat, for oysters, clams and mus
Page 22 and 23: along with the once generated by th
Page 24 and 25: CHAPTER-2 DEVELOPMENT OF MICROBIAL
Page 26 and 27: incubated over magnetic stirrer and
Page 28 and 29: 2.2.2. Isolation of heterotrophic b
Page 31 and 32: The above medium was aseptically di
Page 33: polyphenol content in each flask wa
Page 38 and 39: 2.2.7.e. Lipolysis Tween compounds
Page 40 and 41: alternative method described by Jay
Page 42 and 43: 2.2.8.b Enrichment medium Freshly s
Page 45 and 46: was used. The above test medium was
Page 47 and 48: 2.2.9.a. The enrichment system. The
Page 49: Segregation of potent strains As de
Page 52: Pseudomonas, Acinetobacter, Microco
Page 55 and 56: In a similar manner from the fungal
Page 58 and 59: Precisely, the collection of bacter
Page 60: Table 2.2 Segregation of polyphenol
Page 63 and 64: Table 2.. 5 continued SI. Sample-St
Page 66: Table 2.7 Enrichment, isolation, pr
Page 69 and 70: Table 2.10 Secondary screening of s
Page 71 and 72: Table 2.12 Secondary Screening of t
Page 73: Table 2.14. Fungal Cultures finally
Page 77 and 78: have already been developed and as
Page 79 and 80: MLSS Prepared a pad with asbestos s
Page 83 and 84: connected to the retting reactor th
Page 85:
and Curds, 1971.,Pike and Carringto
Page 89 and 90:
When air is passed through the pipe
Page 92:
Table 3.1. Bacterial Cultures final
Page 99 and 100:
CHAPTER 4 PACKED BED REACTOR 4.1 IN
Page 101 and 102:
polyphenol uptake as exhibited by t
Page 103 and 104:
down ward percolating through the c
Page 105 and 106:
ionic or hydrophobic interactions.
Page 107 and 108:
1987.,Stenstonm, 1989.,)In this cas
Page 109:
Table 4.1 Bacterial and fnngal Cult
Page 112 and 113:
Fig.4.3 Photograph showing efficacy
Page 114:
CHAPTER-5 CONCLUSION
Page 119 and 120:
• From the segregated 33 bacteria
Page 121 and 122:
• To carry out the ret liquor tre
Page 123 and 124:
• On applying the consortium in t
Page 126 and 127:
REFERENCES
Page 128 and 129:
APHA.,1989. Standard methods for th
Page 130 and 131:
Costerton, J.W., Irvin, R. T., and
Page 132 and 133:
Humphries,M., Nemcek,J., Cantwell,
Page 134 and 135:
dissolution and its implica- tions
Page 136:
Reid,G., Jewett, M.A.S., Nickel, r,
show all

"Development of microbial treatment of ret liquor generated in a coir ...

Create successful ePaper yourself

Delete template?

Save as template?