Applied Microbiology and Biotechnology

, Volume 66, Issue 4, pp 408–413

Identification of Pyrococcus furiosus amylopullulanase catalytic residues

Applied Genetics and Molecular Biotechnology

DOI: 10.1007/s00253-004-1690-7

Cite this article as:
Kang, S., Vieille, C. & Zeikus, J.G. Appl Microbiol Biotechnol (2005) 66: 408. doi:10.1007/s00253-004-1690-7
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Abstract

Pyrococcus furiosus amylopullulanase (PfAPU) belongs to glycosyl hydrolase family 57. Using sequence alignments of the known family 57 enzymes and site-directed mutagenesis, E291, D394, and E396 were identified as PfAPU putative catalytic residues. The apparent catalytic efficiencies (kcat/Km) of PfAPU mutants E291Q and D394N on pullulan were 123.0 and 24.4 times lower, respectively, than that of PfAPU. The activity of mutant E396Q on pullulan was too low to allow reliable determination of its catalytic efficiency. The apparent specific activities of these enzymes on starch also decreased 91.0 times (E291Q), 11.7 times (D394N), and 37.2 times (E396Q). The hydrolytic patterns for pullulan and starch were the same, while the hydrolysis rates differed as reported. Based on sequence alignment and a previous report, E291 is proposed as the catalytic nucleophile.

Copyright information

© Springer-Verlag 2004

Authors and Affiliations

  1. 1.Department of Biochemistry and Molecular BiologyMichigan State UniversityEast LansingUSA
  2. 2.Department of Food Science and Human NutritionMichigan State UniversityEast LansingUSA