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来自[具体物种名称未给出]的粉色蛋白(PsPCP)及其物种特异性色素蛋白的基因克隆对子实体的着色有效。

Gene cloning of the pink-colored protein from (PsPCP) and its species-specific chromoprotein are effective for colorization of the fruit body.

作者信息

Fukuta Yasuhisa, Kamei Kengo, Matsui Aoi, Fuji Yosuke, Onuma Hiroki, Shirasaka Norifumi

机构信息

a Department of Applied Biological Chemistry, Faculty of Agriculture , Kindai University , Nara , Japan.

出版信息

Biosci Biotechnol Biochem. 2019 Jul;83(7):1354-1361. doi: 10.1080/09168451.2019.1611406. Epub 2019 May 6.

DOI:10.1080/09168451.2019.1611406
PMID:31056006
Abstract

is a pink mushroom. This pink color is a protein and forms a complex with 3H-indol-3-one. The gene encoding the pink-colored protein from (PsPCP) was cloned, and its sequence was elucidated as a 681-bp. The ORF encodes 226 amino acid residues. The amino acid sequence of the protein did not show any significant homology in the DDBJ/EMBL/GenBank databases. Recombinant PsPCP was expressed as the soluble form in . The reaction mixture of purified recombinant PsPCP and 3H-indol-3-one showed a pink color as the native pigment. A real-time PCR analysis revealed the strong expression of PsPCP in the primordium formation stage of the life cycle of the fungus; however, its expression decreased with the maturation of the fruit body. A comparison of PsPCP gene expression profiles between two strains revealed high levels in the dark-colored strain.

摘要

是一种粉红色蘑菇。这种粉红色是一种蛋白质,它与3H-吲哚-3-酮形成复合物。克隆了来自(PsPCP)的编码粉红色蛋白质的基因,其序列被阐明为681个碱基对。开放阅读框编码226个氨基酸残基。该蛋白质的氨基酸序列在DDBJ/EMBL/GenBank数据库中未显示出任何显著的同源性。重组PsPCP以可溶形式在中表达。纯化的重组PsPCP与3H-吲哚-3-酮的反应混合物呈现出与天然色素相同的粉红色。实时PCR分析显示,PsPCP在真菌生命周期的原基形成阶段强烈表达;然而,随着子实体的成熟,其表达下降。两个菌株之间PsPCP基因表达谱的比较显示深色菌株中的表达水平较高。

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引用本文的文献

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Crystal Structure of the Native Chromoprotein from Provides Insights into the Pigmentation Mechanism.天然色蛋白晶体结构为色素形成机制提供了线索。
J Agric Food Chem. 2024 Aug 7;72(31):17626-17632. doi: 10.1021/acs.jafc.4c02951. Epub 2024 Jul 29.
2
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Bioinform Biol Insights. 2023 Feb 8;17:11779322231154139. doi: 10.1177/11779322231154139. eCollection 2023.