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用于洗衣行业的酶:挖掘碱性蛋白酶的巨大宏基因组库。

Enzymes for the laundry industries: tapping the vast metagenomic pool of alkaline proteases.

作者信息

Niehaus F, Gabor E, Wieland S, Siegert P, Maurer K H, Eck J

机构信息

Biotechnology Research and Information Network, Darmstädter Straße 34-36, D-64673 Zwingenberg, Germany.

出版信息

Microb Biotechnol. 2011 Nov;4(6):767-76. doi: 10.1111/j.1751-7915.2011.00279.x. Epub 2011 Sep 6.

Abstract

In the wide field of laundry and cleaning applications, there is an unbroken need for novel detergent proteases excelling in high stability and activity and a suitable substrate range. We demonstrated the large amount of highly diverse subtilase sequences present in metagenomic DNA by recovering 57 non-redundant subtilase sequence tags with degenerate primers. Furthermore, an activity- as well as a sequence homology-based screening of metagenomic DNA libraries was carried out, using alkaline soil and habitat enrichments as a source of DNA. In this way, 18 diverse full-length protease genes were recovered, sharing only 37-85% of their amino acid residues with already known protease genes. Active clones were biochemically characterized and subjected to a laundry application assay, leading to the identification of three promising detergent proteases. According to sequence similarity, two proteases (HP53 and HP70) can be classified as subtilases, while the third enzyme (HP23) belongs to chymotrypsin-like S1 serine proteases, a class of enzymes that has not yet been described for the use in laundry and cleaning applications.

摘要

在广阔的洗衣和清洁应用领域,一直以来都迫切需要新型洗涤剂蛋白酶,这类蛋白酶需具备高稳定性、高活性以及合适的底物范围。我们通过用简并引物回收57个非冗余枯草杆菌蛋白酶序列标签,证明了宏基因组DNA中存在大量高度多样的枯草杆菌蛋白酶序列。此外,以碱性土壤和生境富集物作为DNA来源,对宏基因组DNA文库进行了基于活性和序列同源性的筛选。通过这种方式,回收了18个不同的全长蛋白酶基因,它们与已知蛋白酶基因的氨基酸残基仅有37% - 85%的同源性。对活性克隆进行了生化特性分析,并进行了洗衣应用测试,从而鉴定出三种有前景的洗涤剂蛋白酶。根据序列相似性,两种蛋白酶(HP53和HP70)可归类为枯草杆菌蛋白酶,而第三种酶(HP23)属于胰凝乳蛋白酶样S1丝氨酸蛋白酶,这是一类尚未被描述用于洗衣和清洁应用的酶。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5d1/3815412/60d684887f16/mbt0004-0767-f1.jpg

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