Silica precipitation with synthetic silaffin peptides

Wieneke, Ralph and Bernecker, Anja and Riedel, Radostan and Sumper, Manfred and Steinem, Claudia and Geyer, Armin (2011) Silica precipitation with synthetic silaffin peptides. ORGANIC & BIOMOLECULAR CHEMISTRY, 9 (15). pp. 5482-5486. ISSN 1477-0520,

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Abstract

Silaffins are highly charged proteins which are one of the major contributing compounds that are thought to be responsible for the formation of the hierarchically structured silica-based cell walls of diatoms. Here we describe the synthesis of an oligo-propyleneamine substituted lysine derivative and its incorporation into the KXXK peptide motif occurring repeatedly in silaffins. N(epsilon)-alkylation of lysine was achieved by a Mitsunobu reaction to obtain a protected lysine derivative which is convenient for solid phase peptide synthesis. Quantitative silica precipitation experiments together with structural information about the precipitated silica structures gained by scanning electron microscopy revealed a dependence of the amount and form of the silica precipitates on the peptide structure.

Item Type: Article
Uncontrolled Keywords: DIATOM THALASSIOSIRA-PSEUDONANA; MORPHOGENESIS; POLYAMINES; MORPHOLOGY; BIOSILICA;
Subjects: 500 Science > 570 Life sciences
Divisions: Biology, Preclinical Medicine > Institut für Biochemie, Genetik und Mikrobiologie > Alumni or Retired > Prof. Dr. Manfred Sumper
Depositing User: Dr. Gernot Deinzer
Date Deposited: 01 Jul 2020 10:26
Last Modified: 01 Jul 2020 10:26
URI: https://pred.uni-regensburg.de/id/eprint/21646

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