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Characterization of Pacific whiting proteinase P-II and partial cloning of cathepsins L and K cDNA from rainbow trout liver

Proteinase P-II purified from parasitized Pacific whiting muscle was previously
identified to be one form of cathepsin L. It appeared to be present in three isozymatic
forms on non-denaturing PAGE gel stained for activity. Its autolytic degradation was
observed on SDS-PAGE gel under its optimum condition, 55°C and pH 5.5, in the
absence of substrate. Amino acid composition analysis revealed that this enzyme had a
considerably greater proportion of hydrophobic amino acids than cathepsin L from other
fish species, and monosaccharide analysis showed it was not glycosylated. The N-terminal
amino acid sequence of the enzyme was 60-65% identical with cathepsin L from
chicken and mammalian species, but only 39% identical with mammalian cathepsin B.
The moderate identity of the N-terminal amino acid sequence of P-II with other cathepsin
L revealed that this cysteine proteinase from Pacific whiting might be encoded by a
cathepsin L-related gene.
Two degenerate primers were designed to clone cathepsins cDNA from rainbow
trout. The 500-bp PCR product from rainbow trout liver cDNA contained at least three different cysteine proteinase sequences, referred to as SFL2, SFL5, and SFL17. SFL5
was the partial cDNA of trout cathepsin L, which was over 80% identical with chicken
cathepsin L amino acid sequence. SFL5 was labeled with Dig-11-dUTP and used to
screen a trout liver cDNA library. One positive clone referred to as LC was identified
and contained a 700-bp insertion overlapping with SFL5. By combining the two
overlapping sequences, a 895-bp cDNA sequence was identified, which included 88%
of the mature enzyme and a 307-bp 3' end untranslated part. Its deduced amino acid
sequences had 83% identity, 91% similarity with chicken cathepsin L and 73% identity,
86% similarity with human cathepsin L. SFL2 might be the partial cDNA of a novel
cathepsin L-related cysteine proteinase. SFL17 may be the partial cDNA of trout
cathepsin K. It had 70% identity and 89% similarity with rabbit and human cathepsin
K at the amino acid level. / Graduation date: 1996

Identiferoai:union.ndltd.org:ORGSU/oai:ir.library.oregonstate.edu:1957/27093
Date25 April 1996
CreatorsNickel, Xianbin F.
ContributorsAn, Haejung
Source SetsOregon State University
Languageen_US
Detected LanguageEnglish
TypeThesis/Dissertation

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