Title: | Human lysozyme secretion increased by alpha-factor pro-sequence in Pichia pastoris |
Author(s): | Oka C; Tanaka M; Muraki M; Harata K; Suzuki K; Jigami Y; |
Address: | "Chiba Prefectural Industrial Research Institute, Chiba, Japan. coka@iri.pref.chiba.jp" |
Journal Title: | Biosci Biotechnol Biochem |
ISSN/ISBN: | 0916-8451 (Print) 0916-8451 (Linking) |
Abstract: | "To get high level secretion of human lysozyme in Pichia pastoris, the following three signal sequences and one prepro sequence were evaluated: chicken lysozyme signal peptide, leucine-rich artificial signal peptide, Saccharomyces invertase signal peptide, and Saccharomyces prepro sequence of alpha factor (MF-alpha Prepro). Transformants harboring a lysozyme gene with MF-alpha Prepro secreted 20-fold more lysozyme than those harboring the lysozyme gene with any one of the other three signal sequences. Three mutant leader sequences derived from MF-alpha Prepro were constructed to discover the function of the pro region. The secretion was dramatically decreased by eliminating the pro region of MF-alpha Prepro. In contrast, MF-alpha Prepro with the EAEAEA sequence directed the secretion of an equivalent level of lysozyme having the extra amino acids (EAEAEA) in its N-terminus. For the effective secretion of native human lysozyme, MF-alpha Prepro without any spacer sequences was most suitable. The secreted protein by MF-alpha Prepro construct was identical with the authentic human lysozyme, judging from N-terminal amino acid sequencing and molecular mass spectrometric and crystallographic analysis" |
Keywords: | "Amino Acid Sequence Animals Base Sequence Chickens Cloning, Molecular/methods DNA Primers Glycoside Hydrolases/genetics Humans Mating Factor Molecular Sequence Data Muramidase/*biosynthesis/chemistry/*genetics Peptides/*genetics Pheromones/genetics *Pichi;" |
Notes: | "MedlineOka, C Tanaka, M Muraki, M Harata, K Suzuki, K Jigami, Y eng England 2000/01/15 Biosci Biotechnol Biochem. 1999 Nov; 63(11):1977-83. doi: 10.1271/bbb.63.1977" |