Item type |
デフォルトアイテムタイプ_(フル)(1) |
公開日 |
2023-03-18 |
タイトル |
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タイトル |
Immunological detection of alkaline-diaminobenzidine-negative peroxisomes of the nematode Caenorhabditis elegans: Purification and unique pH optima of peroxisomal catalase |
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言語 |
en |
作成者 |
Togo, Summanuna H.
Maebuchi, Motohiro
Yokota, Sadaki
Bun-ya, Masanori
Kawahara, Akira
Kamiryo, Tatsuyuki
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アクセス権 |
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アクセス権 |
open access |
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アクセス権URI |
http://purl.org/coar/access_right/c_abf2 |
権利情報 |
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権利情報 |
Copyright (c) 1990 Federation of European Biochemical Societies |
主題 |
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主題Scheme |
Other |
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主題 |
Caenorhabditis elegans |
主題 |
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主題Scheme |
Other |
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主題 |
catalase |
主題 |
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主題Scheme |
Other |
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主題 |
3.3'-diaminobenzidine |
主題 |
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主題Scheme |
Other |
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主題 |
peroxidase |
主題 |
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主題Scheme |
Other |
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主題 |
peroxisomes |
主題 |
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主題Scheme |
NDC |
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主題 |
460 |
内容記述 |
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内容記述 |
We purified catalase-2 of the nematode Caenorhabditis elegans and identified peroxisomes in this organism. The peroxisomes of C. elegans were not detectable by cytochemical staining using 3,3'-diaminobenzidine, a commonly used method depending on the peroxidase activity of peroxisomal catalase at pH 9 in which genuine peroxidases are inactive. The cDNA sequences of C. elegans predict two catalases very similar to each other throughout the molecule, except for the short C-terminal sequence; catalase-2 (500 residues long) carries a peroxisomal targeting signal 1-like sequence (Ser-His-Ile), whereas catalase-1 does not. The catalase purified to near homogeneity from the homogenate of C. elegans cells consisted of a subunit of 57 kDa and was specifically recognized by anti-(catalase-2) serum but not by anti-(catalase-1) serum. Subcellular fractionation and indirect immunoelectron microscopy of the nematode detected catalase-2 inside vesicles judged to be peroxisomes using morphological criteria. The purified enzyme (220 kDa) was tetrameric, similar to many catalases from various sources, but exhibited unique pH optima for catalase (pH 6) and peroxidase (pH 4) activities; the latter value is unusually low and explains why the peroxidase activity was undetectable using the standard alkaline diaminobenzidine- staining method. These results indicate that catalase-2 is peroxisomal and verify that it can be used as a marker enzyme for C. elegans peroxisomes. |
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言語 |
en |
出版者 |
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出版者 |
Federation of European Biochemical Societies |
言語 |
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言語 |
eng |
資源タイプ |
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資源タイプ識別子 |
http://purl.org/coar/resource_type/c_6501 |
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資源タイプ |
journal article |
出版タイプ |
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出版タイプ |
VoR |
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出版タイプResource |
http://purl.org/coar/version/c_970fb48d4fbd8a85 |
関連情報 |
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識別子タイプ |
PMID |
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関連識別子 |
10691967 |
関連情報 |
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識別子タイプ |
DOI |
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関連識別子 |
10.1046/j.1432-1327.2000.01091.x |
関連情報 |
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関連タイプ |
isVersionOf |
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識別子タイプ |
DOI |
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関連識別子 |
http://dx.doi.org/10.1046/j.1432-1327.2000.01091.x |
収録物識別子 |
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収録物識別子タイプ |
ISSN |
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収録物識別子 |
0014-2956 |
収録物識別子 |
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収録物識別子タイプ |
NCID |
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収録物識別子 |
AA00639541 |
開始ページ |
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開始ページ |
1307 |
書誌情報 |
European Journal of Biochemistry
European Journal of Biochemistry
巻 267,
号 5,
p. 1307-1312,
発行日 2000
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旧ID |
14889 |