Two-Dimensional Fluorescence Spectroscopy: A New Tool for On-Line Bioprocess Monitoring

Research output: Contribution to journalArticleResearchpeer review

Authors

Research Organisations

View graph of relations

Details

Original languageEnglish
Pages (from-to)63-74
Number of pages12
JournalBiotechnology progress
Volume14
Issue number1
Publication statusPublished - 1998

Abstract

Two-dimensional fluorescence spectroscopy is presented as a new method for bioprocess monitoring. It covers a wide range of excitation and emission wavelengths and is a further development of the fluorescence measurements performed so far, which concentrated mainly on NAD(P)H culture fluorescence. Biogenic fluorophores such as proteins, coenzymes, and vitamins can simultaneously be detected qualitatively and quantitatively inside and outside the cells. This optical method is noninvasive, suitable for in vive measurements. One whole spectrum (excitation, 250-550 nm; emission, 260-600 nm) with the described parameters is performed within 1 min, which allows an almost continuous monitoring of the bioprocess. The technique is ideal for on-line, in situ measurements via fiber optical systems. Results are presented for cultivations of Claviceps purpurea, Escherichia coli, Saccharomyces cerevisiae, and Sphingomonas yanoikuyae. Cell growth and the metabolism of the cells (changes from aerobic to anaerobic conditions and uncoupling of the oxidative phosphorylation) could be detected.

ASJC Scopus subject areas

Cite this

Two-Dimensional Fluorescence Spectroscopy: A New Tool for On-Line Bioprocess Monitoring. / Marose, Stefan; Lindemann, Carsten; Scheper, Thomas.
In: Biotechnology progress, Vol. 14, No. 1, 1998, p. 63-74.

Research output: Contribution to journalArticleResearchpeer review

Download
@article{bdd637a69ca44763b7761b6d1398b223,
title = "Two-Dimensional Fluorescence Spectroscopy: A New Tool for On-Line Bioprocess Monitoring",
abstract = "Two-dimensional fluorescence spectroscopy is presented as a new method for bioprocess monitoring. It covers a wide range of excitation and emission wavelengths and is a further development of the fluorescence measurements performed so far, which concentrated mainly on NAD(P)H culture fluorescence. Biogenic fluorophores such as proteins, coenzymes, and vitamins can simultaneously be detected qualitatively and quantitatively inside and outside the cells. This optical method is noninvasive, suitable for in vive measurements. One whole spectrum (excitation, 250-550 nm; emission, 260-600 nm) with the described parameters is performed within 1 min, which allows an almost continuous monitoring of the bioprocess. The technique is ideal for on-line, in situ measurements via fiber optical systems. Results are presented for cultivations of Claviceps purpurea, Escherichia coli, Saccharomyces cerevisiae, and Sphingomonas yanoikuyae. Cell growth and the metabolism of the cells (changes from aerobic to anaerobic conditions and uncoupling of the oxidative phosphorylation) could be detected.",
author = "Stefan Marose and Carsten Lindemann and Thomas Scheper",
year = "1998",
doi = "10.1021/bp970124o",
language = "English",
volume = "14",
pages = "63--74",
journal = "Biotechnology progress",
issn = "8756-7938",
publisher = "Wiley-Blackwell",
number = "1",

}

Download

TY - JOUR

T1 - Two-Dimensional Fluorescence Spectroscopy: A New Tool for On-Line Bioprocess Monitoring

AU - Marose, Stefan

AU - Lindemann, Carsten

AU - Scheper, Thomas

PY - 1998

Y1 - 1998

N2 - Two-dimensional fluorescence spectroscopy is presented as a new method for bioprocess monitoring. It covers a wide range of excitation and emission wavelengths and is a further development of the fluorescence measurements performed so far, which concentrated mainly on NAD(P)H culture fluorescence. Biogenic fluorophores such as proteins, coenzymes, and vitamins can simultaneously be detected qualitatively and quantitatively inside and outside the cells. This optical method is noninvasive, suitable for in vive measurements. One whole spectrum (excitation, 250-550 nm; emission, 260-600 nm) with the described parameters is performed within 1 min, which allows an almost continuous monitoring of the bioprocess. The technique is ideal for on-line, in situ measurements via fiber optical systems. Results are presented for cultivations of Claviceps purpurea, Escherichia coli, Saccharomyces cerevisiae, and Sphingomonas yanoikuyae. Cell growth and the metabolism of the cells (changes from aerobic to anaerobic conditions and uncoupling of the oxidative phosphorylation) could be detected.

AB - Two-dimensional fluorescence spectroscopy is presented as a new method for bioprocess monitoring. It covers a wide range of excitation and emission wavelengths and is a further development of the fluorescence measurements performed so far, which concentrated mainly on NAD(P)H culture fluorescence. Biogenic fluorophores such as proteins, coenzymes, and vitamins can simultaneously be detected qualitatively and quantitatively inside and outside the cells. This optical method is noninvasive, suitable for in vive measurements. One whole spectrum (excitation, 250-550 nm; emission, 260-600 nm) with the described parameters is performed within 1 min, which allows an almost continuous monitoring of the bioprocess. The technique is ideal for on-line, in situ measurements via fiber optical systems. Results are presented for cultivations of Claviceps purpurea, Escherichia coli, Saccharomyces cerevisiae, and Sphingomonas yanoikuyae. Cell growth and the metabolism of the cells (changes from aerobic to anaerobic conditions and uncoupling of the oxidative phosphorylation) could be detected.

UR - http://www.scopus.com/inward/record.url?scp=0031907915&partnerID=8YFLogxK

U2 - 10.1021/bp970124o

DO - 10.1021/bp970124o

M3 - Article

C2 - 9496670

AN - SCOPUS:0031907915

VL - 14

SP - 63

EP - 74

JO - Biotechnology progress

JF - Biotechnology progress

SN - 8756-7938

IS - 1

ER -

By the same author(s)