Determination of redox potential levels critical for cell respiration and suitable forL‐leucine production
作者:
Kunihiko Akashi,
Shigeho Ikeda,
Hiroshiro Shibai,
Kaetsu Kobayashi,
Yoshio Hirose,
期刊:
Biotechnology and Bioengineering
(WILEY Available online 1978)
卷期:
Volume 20,
issue 1
页码: 27-41
ISSN:0006-3592
年代: 1978
DOI:10.1002/bit.260200104
出版商: Wiley Subscription Services, Inc., A Wiley Company
数据来源: WILEY
摘要:
AbstractThe effect of oxygen supply onL‐leucine fermentation was investigated employing a leucine‐producing mutant ofBrevibacterium lactofermentum. Since it was not possible to measure oxygen tension below 0.01 atm by a Teflon‐coated oxygen electrode, the degree of satisfaction of the cells' oxygen demand (cells' respiration rate/maximum oxygen demand of cells,rab/KrM) and the redox potential of the culture medium (E.mV) were used as indices to oxygen supply in cultures under low oxygen tension. When the oxygen demand of the cells was satisfied (rab/KrM= 1.0) and theEvalue was between −90 and −110 mV,L‐leucine formation was 26.5 mg‐ml. When the oxygen demand of the cells was not satisfied (rab/KrM= 0.85) and theEvalue was between −200 and −220mV,L‐leucine accumulation was 29.7 mg/ml. When the oxygen supply was extremely limited (rab/KrM= 0.27) and theEvalue was −280 mV.L‐leucine formation was 12.9 mg/ml. A new method which simultaneously measures the redox potential and dissolved oxygen was applied to the determination of the critical dissolved oxygen level for cell respiration (PLcrit), which was too small to be detected by conventional oxygen electrodes. The value ofPLcritof the leucine producer was
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