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Updated: Oct 2, 2026

Measuring Gene Expression in Bombarded Barley Aleurone Layers with Increased Throughput
Published on: March 30, 2018
Expression, purification and preliminary crystallographic studies of alpha-amylase isozyme 1 from barley seeds
Xavier Robert1, Tine E Gottschalk, Richard Haser
1Institut de Biologie et Chimie des Protéines, Laboratoire de Bio-Cristallographie CNRS-UMR 5086, 69367 Lyon CEDEX 07, France.
Abstract:
The germinating barley seed contains two major alpha-amylase isozyme families, AMY1 and AMY2, involved in starch degradation to provide energy used by the plant embryo for growth. Many years of difficulty in growing three-dimensional crystals of natural AMY1 have now been overcome by a nonapeptide truncation of the enzyme C-terminus. The truncated enzyme was overexpressed in Pichia pastoris, purified and crystallized by the hanging-drop vapour-diffusion method using polyethylene glycol 8000 as precipitant and 2-propanol as an additive. Crystals belong to the orthorhombic space group P2(1)2(1)2, with unit-cell parameters a = 88.36, b = 72.82, c = 61.74 A and one molecule per asymmetric unit.
