Literature DB >> 23999260

Carrier free co-immobilization of alpha amylase, glucoamylase and pullulanase as combined cross-linked enzyme aggregates (combi-CLEAs): a tri-enzyme biocatalyst with one pot starch hydrolytic activity.

Sachin Talekar1, Amol Pandharbale2, Mayur Ladole3, Shamraja Nadar3, Mosin Mulla3, Kshitija Japhalekar3, Kishori Pattankude3, Devika Arage3.   

Abstract

A tri-enzyme biocatalyst "combi-CLEAs" with starch hydrolytic activity was prepared from commercially available alpha amylase, glucoamylase and pullulanase preparations by aggregating enzymes with ammonium sulphate followed by cross-linking formed aggregates for 4.5h with 40 mM glutaraldehyde. The effects of precipitant type and cross-linking were studied and the biocatalyst was characterized. Scanning electron microscopy analysis showed that tri-enzyme biocatalyst was of spherical structure. For one pot starch hydrolytic activity, shift in optimum pH from 6 to 7 and temperature from 65 to 75 °C were observed after co-immobilization of enzymes. After one pot starch hydrolysis reaction in batch mode, 100%, 60% and 40% conversions were obtained with combi-CLEAs, separate CLEAs mixture and free enzyme mixture, respectively. Co-immobilization also enhanced the thermal stability of enzymes. Finally, the catalytic activity of enzymes in combi-CLEAs during one pot starch hydrolysis was well maintained up to five cycles without performance changes.
Copyright © 2013 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Alpha amylase; Combined cross-linked enzyme aggregates (combi-CLEAs); Glucoamylase; One pot starch hydrolysis; Pullulanase

Mesh:

Substances:

Year:  2013        PMID: 23999260     DOI: 10.1016/j.biortech.2013.08.035

Source DB:  PubMed          Journal:  Bioresour Technol        ISSN: 0960-8524            Impact factor:   9.642


  8 in total

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7.  Downsizing a pullulanase to a small molecule with improved soluble expression and secretion efficiency in Escherichia coli.

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  8 in total

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