Fine-tuned preparation of cross-linked laccase nanoaggregates
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Sahutoglu, Arif Sercan
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Canakkale Onsekiz Mart Univ, Dept Chem, Fac Arts & Sci, TR-17100 Canakkale, TurkeyCanakkale Onsekiz Mart Univ, Dept Chem, Fac Arts & Sci, TR-17100 Canakkale, Turkey
Sahutoglu, Arif Sercan
[1
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Akgul, Cahit
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Canakkale Onsekiz Mart Univ, Dept Chem, Fac Arts & Sci, TR-17100 Canakkale, TurkeyCanakkale Onsekiz Mart Univ, Dept Chem, Fac Arts & Sci, TR-17100 Canakkale, Turkey
Akgul, Cahit
[1
]
机构:
[1] Canakkale Onsekiz Mart Univ, Dept Chem, Fac Arts & Sci, TR-17100 Canakkale, Turkey
This study focuses on well-known but commonly overlooked or unreported factors in the preparation of cross-linked enzyme nano-aggregates (nano-CLEAs). The parameters including the ionic strength of the protein solution, protein, precipitant and cross-linker concentrations, pH and addition order of the reagents were fine-tuned for nanoaggregate preparation without the need of non-protein support material, special equipment or sophisticated procedures. For this purpose, precipitation as nano-aggregates and then cross-linking while maintaining submicron size distribution were studied independently. Moreover, nano-aggregate formation from reverse micellar solutions was also investigated to improve the scope of the method to membrane-bound enzymes. Five different precipitation agents together with three different cross-linkers were investigated for immobilization of the Trametes versicolor laccase as cross-linked nano-aggregates. Although complete activity recovery was possible for micro-aggregates, the best activity results for nano-aggregates were 40.5%+/- 5.0. The K-m values of the immobilized enzymes were slightly lower than the K-m values of the free counterparts which indicate little or no mass transfer limitation due to the nano-immobilization process. However, V-max values were also lower. The activity loss and V-max reduction upon immobilization were found to mainly result from the modification of the amine groups instead of excess crosslinking. The thermal stabilities of the crosslinked laccase nano-aggregates were significantly higher (similar to 10-30 fold at 60 degrees C) compared to free laccase and the nano-CLEAs retained up to 30% of their initial activities upon 7 consequent usages. The sizes of the obtained immobilized enzyme products were found to be greatly variable depending on the cross-linker type. The smaller particles (similar to 200 nm radius) were obtained when EDAC was used as the cross-linker. The larger products (similar to 600 nm radius) were prepared when the cross-linker was dextran poly-aldehyde. The addition order of the reagents was found to be effective on particle size and thermal stability values.
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Anna Univ, Dept Appl Sci & Technol, Environm Management Lab, AC Tech, Madras 600025, Tamil Nadu, India
SRM Univ, Sch Bioengn, Dept Biotechnol, Madras 603203, Tamil Nadu, IndiaAnna Univ, Dept Appl Sci & Technol, Environm Management Lab, AC Tech, Madras 600025, Tamil Nadu, India
Kumar, Vaidyanathan Vinoth
Sivanesan, Subramanian
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Anna Univ, Dept Appl Sci & Technol, Environm Management Lab, AC Tech, Madras 600025, Tamil Nadu, IndiaAnna Univ, Dept Appl Sci & Technol, Environm Management Lab, AC Tech, Madras 600025, Tamil Nadu, India
Sivanesan, Subramanian
Cabana, Hubert
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Univ Sherbrooke, Dept Civil Engn, Sherbrooke, PQ J1K 2R1, CanadaAnna Univ, Dept Appl Sci & Technol, Environm Management Lab, AC Tech, Madras 600025, Tamil Nadu, India
机构:
Univ Tehran, Coll Sci, Sch Biol, PBRL, Tehran, Iran
Univ Tehran Med Sci, Fac Pharm, Dept Pharmaceut Biotechnol, Tehran, Iran
Univ Tehran Med Sci, Biotechnol Res Ctr, Tehran, IranUniv Tehran, Coll Sci, Sch Biol, PBRL, Tehran, Iran
Fathali, Zahra
Rezaei, Shahla
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Univ Tehran Med Sci, Fac Pharm, Dept Pharmaceut Biotechnol, Tehran, Iran
Univ Tehran Med Sci, Biotechnol Res Ctr, Tehran, IranUniv Tehran, Coll Sci, Sch Biol, PBRL, Tehran, Iran
Rezaei, Shahla
Faramarzi, Mohammad Ali
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Univ Tehran Med Sci, Fac Pharm, Dept Pharmaceut Biotechnol, Tehran, Iran
Univ Tehran Med Sci, Biotechnol Res Ctr, Tehran, IranUniv Tehran, Coll Sci, Sch Biol, PBRL, Tehran, Iran
机构:
Indian Inst Technol Delhi, Dept Chem, Enzyme Technol Lab, New Delhi 110016, IndiaIndian Inst Technol Delhi, Dept Chem, Enzyme Technol Lab, New Delhi 110016, India
Dey, Bipasa
Panwar, Varsha
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Indian Inst Technol Delhi, Dept Chem, Enzyme Technol Lab, New Delhi 110016, IndiaIndian Inst Technol Delhi, Dept Chem, Enzyme Technol Lab, New Delhi 110016, India
Panwar, Varsha
Dutta, Tanmay
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Indian Inst Technol Delhi, Dept Chem, Enzyme Technol Lab, New Delhi 110016, India
Indian Inst Technol, Dept Chem, MS 731, New Delhi 110016, IndiaIndian Inst Technol Delhi, Dept Chem, Enzyme Technol Lab, New Delhi 110016, India