Regeneration of NAD(P)H by immobilized whole cells of Clostridium butyricum under hydrogen high pressure

Tadashi Matsunaga*, Naoki Matsunaga, Shigeo Nishimura

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

21 Citations (Scopus)

Abstract

Immobilized whole cells of Clostridium butyricum reduced both NAD+ and NADP+ in the presence of hydrogen at a pressure of 100 atm. The NAD+ and NADP+ reduction activities were 4.45 and 4.30 U/g dry cells, respectively [U = NAD(P)H regenerated, μ mol/min]. The amount of NADH regenerated by immobilized cells increased with increasing hydrogen pressure above 10 atm. Immobilized cells (6 mg dry cells) of Cl. butyricum completely converted NAD+ (6.4 μmole) to NADH for 5 h, whereas only 60% of NAD+ were reduced by free cells. Immobilized cells retained 89% activity after the 5‐h reactions were repeated 4 times. L‐Alanine was continuously produced at the rate of 12.8 μmol/min g dry cells from hydrogen, ammonium, and pyruvate with immobilized Cl. butyricum‐alanine dehydrogenase.

Original languageEnglish
Pages (from-to)1277-1281
Number of pages5
JournalBiotechnology and Bioengineering
Volume27
Issue number9
DOIs
Publication statusPublished - 1985
Externally publishedYes

ASJC Scopus subject areas

  • Biotechnology
  • Bioengineering
  • Applied Microbiology and Biotechnology

Fingerprint

Dive into the research topics of 'Regeneration of NAD(P)H by immobilized whole cells of Clostridium butyricum under hydrogen high pressure'. Together they form a unique fingerprint.

Cite this