TY - JOUR
T1 - Identification of a novel α-amylase by expression of a newly cloned human amy3 cDNA in yeast
AU - Shiosaki, Kouichi
AU - Takata, Ken ichi
AU - Omichi, Kaoru
AU - Tomita, Naohiro
AU - Horii, Akira
AU - Ogawa, Michio
AU - Matsubara, Kenichi
N1 - Funding Information:
We thankD r. O. Chisakafo r his advicea ndd iscussion and Ms.K . Mimura for heer xcellenste cretariaals sistance. This work was supportedin part by a ScientifRice search grant to K.M. from the JapaneseM inistry of Education, Sciencea nd Culture. Following the acceptanceo f this manuscript,w e learned thatth e humana mylase-encodingge nesa my2 and amy3h ave been determinedt o be identical to AMY2A andA MY2B,r espectivel(yG root etal., 1989).
PY - 1990/5/14
Y1 - 1990/5/14
N2 - A novel amylase gene (amy3) that differs in nucleotide sequence from salivary amylase gene (amyl) and pancreatic amylase gene (amy2) has been described [Tomita et al., Gene 76 (1989) 11-18], but whether this gene can ever code for an active enzyme has not been shown. We prepared cDNA of this gene from an mRNA obtained from lung carcinoid tissue, and expressed it in Saccharomyces cerevisiae under the control of an acid phosphatase promoter. The product was secreted into culture media, and showed enzymatic activity, demonstrating that this novel α-amylase gene (amy3) can code for a functional isozyme. We purified this enzyme, and compared its biological properties with those of salivary and pancreatic human amylases similarly expressed in yeast. We observed that the novel amylase isozyme is more heat-sensitive than others, and that its substrate specificity is different from the other two isozymes.
AB - A novel amylase gene (amy3) that differs in nucleotide sequence from salivary amylase gene (amyl) and pancreatic amylase gene (amy2) has been described [Tomita et al., Gene 76 (1989) 11-18], but whether this gene can ever code for an active enzyme has not been shown. We prepared cDNA of this gene from an mRNA obtained from lung carcinoid tissue, and expressed it in Saccharomyces cerevisiae under the control of an acid phosphatase promoter. The product was secreted into culture media, and showed enzymatic activity, demonstrating that this novel α-amylase gene (amy3) can code for a functional isozyme. We purified this enzyme, and compared its biological properties with those of salivary and pancreatic human amylases similarly expressed in yeast. We observed that the novel amylase isozyme is more heat-sensitive than others, and that its substrate specificity is different from the other two isozymes.
KW - Recombinant DNA
KW - Saccharomyces cerevisiae
KW - acid phosphatase promoter
KW - isozymes
KW - secretion
KW - substrate specificity
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U2 - 10.1016/0378-1119(90)90013-H
DO - 10.1016/0378-1119(90)90013-H
M3 - Article
C2 - 2197187
AN - SCOPUS:0025326755
SN - 0378-1119
VL - 89
SP - 253
EP - 258
JO - Gene
JF - Gene
IS - 2
ER -