Literature DB >> 25286947

Cloning, expression, purification and preliminary X-ray analysis of EstN2, a novel archaeal α/β-hydrolase from Candidatus Nitrososphaera gargensis.

Heidi Kaljunen1, Jennifer Chow2, Wolfgang R Streit2, Jochen Mueller-Dieckmann2.   

Abstract

EstN2 is a novel α/β-hydrolase originating from the ammonia-oxidizing thaumarchaeon Candidatus Nitrososphaera gargensis. The genome of the organism was sequenced and genes conferring putative lipolytic activity were amplified and cloned into Escherichia coli as a heterologous host. Through function-based screening, esterase and lipase activity was detected. A recombinant enzyme designated EstN2 was successfully expressed, purified and crystallized. The crystals belonged to space group I2, with one molecule per asymmetric unit, and diffracted X-rays to 1.5 Å resolution.

Entities:  

Keywords:  Candidatus Nitrososphaera gargensis; EstN2; α/β-hydrolase

Mesh:

Substances:

Year:  2014        PMID: 25286947      PMCID: PMC4188087          DOI: 10.1107/S2053230X14018482

Source DB:  PubMed          Journal:  Acta Crystallogr F Struct Biol Commun        ISSN: 2053-230X            Impact factor:   1.056


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1.  The Thaumarchaeon N. gargensis carries functional bioABD genes and has a promiscuous E. coli ΔbioH-complementing esterase EstN1.

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