J. Lehmbeck

发表

Efficient oligo nucleotide mediated CRISPR-Cas9 gene editing in Aspergilli.

U. Mortensen, C. S. Nødvig, Zofia D Jarczynska, 2018, Fungal genetics and biology : FG & B.

Mutational analysis of the roles in catalysis and substrate recognition of arginines 54 and 305, aspartic acid 309, and tryptophan 317 located at subsites 1 and 2 in glucoamylase from Aspergillus niger.

B. Svensson, T. P. Frandsen, R. Honzatko, 1995, Biochemistry.

Characterization of the Aspergillus niger prtT, a unique regulator of extracellular protease encoding genes.

F. Schuren, P. Punt, C. A. van den Hondel, 2008, Fungal genetics and biology : FG & B.

Cloning, heterologous expression, and enzymatic characterization of a thermostable glucoamylase from Talaromyces emersonii.

T. P. Frandsen, J. Lehmbeck, B. R. Nielsen, 2002, Protein expression and purification.

Identification of a single-copy gene encoding a Type I chlorophyll a/b-binding polypeptide of photosystem I in Arabidopsis thaliana

P. Jensen, M. Kristensen, B. Stummann, 1992 .

A new transcriptional activator for amylase genes in Aspergillus

K. L. Petersen, T. Christensen, J. Lehmbeck, 1999, Molecular and General Genetics MGG.

Sequence of two genes in pea chloroplast DNA coding for 84 and 82 kD polypeptides of the photosystem I complex

O. Rasmussen, B. Stummann, K. W. Henningsen, 2004, Plant Molecular Biology.

Site-directed mutagenesis of the catalytic base glutamic acid 400 in glucoamylase from Aspergillus niger and of tyrosine 48 and glutamine 401, both hydrogen-bonded to the gamma-carboxylate group of glutamic acid 400.

B. Svensson, T. P. Frandsen, M. Sierks, 1994, Biochemistry.

A quick solution: ab initio structure determination of a 19 kDa metalloproteinase using ACORN.

K. Wilson, E. Dodson, P. Østergaard, 2001, Acta crystallographica. Section D, Biological crystallography.

A cDNA clone encoding a 10.8 kDa photosystem I polypeptide of barley

B. Møller, H. Scheller, G. Høyer-Hansen, 1988, FEBS letters.

Isolation and characterisation of genes for sulphate activation and reduction in Aspergillus nidulans: implications for evolution of an allosteric control region by gene duplication

I. G. Clausen, G. Turner, A. Bailey, 1995, Molecular and General Genetics MGG.

Structural and Catalytic Properties of S1 Nuclease from Aspergillus oryzae Responsible for Substrate Recognition, Cleavage, Non–Specificity, and Inhibition

J. Hašek, J. Stránský, P. Lipovová, 2016, PloS one.

Heterologous Expression and Protein Secretion in Filamentous Fungi

J. Lehmbeck, W. Yoder, 2004 .

Nucleotide sequence of the 5.6 kbp psbB operon of pea chloroplast DNA

B. Stummann, K. W. Henningsen, J. Lehmbeck, 1989 .

Nucleotide sequence of the single ribosomal RNA operon of pea chloroplast DNA

B. Stummann, K. W. Henningsen, J. Lehmbeck, 1988 .

Structural and Catalytic Properties of S1 Nuclease from Aspergillus oryzae Responsible for Substrate Recognition, Cleavage, Nonâ•fiSpecificity, and Inhibition

J. Hašek, J. Stránský, P. Lipovová, 2017 .

Glucoamylase mutants in the conserved active-site segment Trp170-Tyr175 located at a distance from the site of catalysis.

B. Svensson, T. P. Frandsen, J. Lehmbeck, 1997, Protein Engineering.

Efficient oligo nucleotide mediated CRISPR-Cas9 gene editing in Aspergilli.

U. Mortensen, C. S. Nødvig, M. E. Kogle, 2018, Fungal genetics and biology : FG & B.