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| 001 | vtls000093770 | ||
| 003 | KUKTEM | ||
| 005 | 20251117113320.0 | ||
| 008 | 160310t2015 my a f 000 0 eng d | ||
| 020 | _aTHE0001045(Local) | ||
| 039 | 9 |
_a201905171307 _bnazirah _c201712061613 _dnazri _y201603101218 _zhuda |
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| 040 | _aUMP | ||
| 090 | _aFKKSA .Y36 2015 r Bc. | ||
| 100 | 0 | _aYana Nuratri | |
| 245 | 1 |
_aAssessing storage stability and mercury reduction of freeze-dried pseudomonas putida within different types of lyoprotectant / _cYana Nuratri |
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| 260 |
_aKuantan, Pahang : _bUMP, _c2015 |
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| 300 |
_axiv, 67 p. : _bill. ; _c30 cm. + _e1 CD-ROM |
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| 500 | _aFaculty of Chemical & Natural Resources Engineering | ||
| 502 | _aProject Paper (Bachelors of Chemical Engineering) -- Universiti Malaysia Pahang – 2015 | ||
| 504 | _aBibliography : p. 51-58 | ||
| 520 | 3 | _aPseudomonas putida is a potential strain in biological treatment to remove mercury contained in the effluent of petrochemical industry due to its mercury reductase enzyme that able to reduce ionic mercury to elementary mercury. Freeze-dried P. putida allows easy, inexpensive shipping, handling and high stability of the product. This study was aimed to freeze dry P. putida cells with addition of lyoprotectant. Lyoprotectant was added into the cells suspension prior to freezing. Dried P. putida obtained was then mixed with synthetic mercury. Viability of recovery P. putida after freeze dry was significantly influenced by the type of lyoprotectant. Among the lyoprotectants, tween 80 / sucrose was found to be the best lyoprotectant. Sucrose able to recover more than 78% (6.2E+09 CFU/ml) of the original cells (7.90E+09CFU/ml) after freeze dry and able to retain 5.40E+05 viable cells after 4 weeks storage in 4oC without vacuum. PEG pre-treated freeze dry cells and broth pre-treated freeze dry cells after freeze-dry recovered more than 64% (5.0 E+09CFU/ml) and >0.1% (5.60E+07CFU/ml). Freeze-dried P. putida cells in PEG and broth cannot survive after 4 weeks storage. Freeze dry also does not really change the pattern of growth P. putida but extension of lag time was found 1 hour after 3 weeks of storage. Additional time was required for freeze-dried P. putida cells to recover before introduce freeze-dried cells to more complicated condition such as mercury solution. The maximum mercury reduction of PEG pre-treated freeze-dried cells after freeze dry and after storage 3 weeks was 56.78% and 17.91 %.The maximum of mercury reduction of tween 80 / sucrose pre-treated freeze-dried cells after freeze dry and after storage 3 weeks were 26.35% and 25.03%. Freeze dried P .putida was found to have lower mercury reduction compare to the fresh P. putida that has been growth in agar. Result from this study may be beneficial and useful as initial reference before commercialize freeze-dried P. putida. | |
| 610 | 2 | 0 |
_aFaculty of Chemical & Natural Resources Engineering _xDissertations |
| 650 | 0 |
_aUniversities and Colleges _xDissertations |
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| 650 | 0 | _aTheses | |
| 856 | 4 | 0 |
_uhttp://ecollib.ump.edu.my/26011/ _zAccess in library only |
| 999 |
_aVIRTUA40 _c6588 _d6594 |
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