ISSN print edition: 0366-6352
ISSN electronic edition: 1336-9075
Registr. No.: MK SR 9/7
Aquaculture by-product: a source of proteolytic enzymes for detergent additives
Chirleanny M. Mendes, Marília A. Brito, Tatiana S. Porto, Ana L. F. Porto, Ranilson S. Bezerra, Luiz B. Carvalho, Ana M. A. Caneiro-Leão, and Maria G. Carneiro-da-Cunha
Departamento de Bioquímica, Universidade Federal de Pernambuco, Campus Universitário, s/n, Cidade Universitária, CEP: 50670-420 Recife, PE, Brazil
Received: 13 March 2009 Revised: 30 May 2009 Accepted: 2 June 2009
Abstract: Intestine proteases of Nile tilapia (Oreochromis niloticus) were partially purified by heat treatment (purification factor of 3.5, enzyme activity remained almost constant) to reach
the maximum activity and stability within an alkaline pH range of 7.2–11.0. The optimum temperature and stability over a 120
min period were found to be at 55°C and at 35–45°C, respectively. The proteases’ activity was not affected by a 1 vol. % saponin
surfactant, inactivated by 0.01 g mL−1 sodium dodecylsulphate after 120 min, and it remained stable for 30 min in a 5 vol. % and 10 vol. % hydrogen peroxide solutions.
The proteases were slightly activated by Ca2+, Mg2+, and K+ and the substrate most effectively hydrolysed was casein (40.0 U mg−1). A 24 full factorial design used to evaluated the influence of independent variables showed that the enzyme extract, detergent
concentration and the incubation time had a significant influence on the enzymatic activity. The best conditions to be used
concerning detergent additive were found with 0.3 mg mL−1 of protein and 3.0 mg mL−1 of detergent for 30 min in the presence of Astrus® detergent.
Keywords: protease - Nile tilapia - laundry detergent - surfactant - oxidising agents
Full paper is available at www.springerlink.com.
Chemical Papers 63 (6) 662–669 (2009)
Monday, December 11, 2023