Literature DB >> 10089330

Crystallization and preliminary x-ray diffraction analysis of hydroxynitrile lyase from cassava (Manihot esculenta).

H Lauble1, K Decanniere, H Wajant, S Förster, F Effenberger.   

Abstract

Hydroxynitrile lyase from M. esculenta (cassava) was crystallized in two different crystal forms by the hanging-drop vapour-diffusion method. Crystals of form I were obtained from a mixture of polyethylene glycol 8000 and 2-methyl-2,4-pentanediol, and belong to the tetragonal space group P41212 or its enantiomorph P43212, with unit-cell parameters a = b = 105.9, c = 188.9 A and with two molecules in the asymmetric unit. These crystals diffract to 2.9 A with conventional X-ray sources and beyond 2.1 A resolution with synchrotron radiation. The crystals are relatively sensitive to radiation damage and conditions for flash-cooling the crystals have been established. A complete native data set has been collected up to 2.2 A resolution. Crystal form II has been obtained at pH 5.6 using lithium sulfate as a precipitant. The crystals apparently belong to the orthorhombic space group P21212, with unit-cell parameters a = 117.52, b = 127.09 and c = 78.08 A, have two molecules in the asymmetric unit and diffract to beyond 2.0 A resolution. A complete native data set has been collected to 2.2 A resolution.

Entities:  

Mesh:

Substances:

Year:  1999        PMID: 10089330     DOI: 10.1107/s0907444998017971

Source DB:  PubMed          Journal:  Acta Crystallogr D Biol Crystallogr        ISSN: 0907-4449


  3 in total

1.  Structure determinants of substrate specificity of hydroxynitrile lyase from Manihot esculenta.

Authors:  Hanspeter Lauble; Burkhard Miehlich; Siegfried Förster; Christoph Kobler; Harald Wajant; Franz Effenberger
Journal:  Protein Sci       Date:  2002-01       Impact factor: 6.725

2.  Mechanistic aspects of cyanogenesis from active-site mutant Ser80Ala of hydroxynitrile lyase from Manihot esculenta in complex with acetone cyanohydrin.

Authors:  H Lauble; B Miehlich; S Förster; H Wajant; F Effenberger
Journal:  Protein Sci       Date:  2001-05       Impact factor: 6.725

3.  Larger active site in an ancestral hydroxynitrile lyase increases catalytically promiscuous esterase activity.

Authors:  Bryan J Jones; Robert L Evans; Nathan J Mylrea; Debayan Chaudhury; Christine Luo; Bo Guan; Colin T Pierce; Wendy R Gordon; Carrie M Wilmot; Romas J Kazlauskas
Journal:  PLoS One       Date:  2020-06-30       Impact factor: 3.240

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.