Table 1.
Strain designation | References or sources | Mutations in polyamine biosynthetic pathway* | Amine content, μmol/g wet weight†
|
|
---|---|---|---|---|
Putrescine | Spermidine | |||
71-18 | 12 | None | 7 | 1.2 |
EWH319 | 13 | Δ(speAspeB) ΔspeC Δ(speDspeE) | 0‡ | 0‡ |
HT306 | 11 | Δ(speAspeB) ΔspeC Δ(speDspeE)cadA | 0‡ | 0‡ |
EWH319/pDT1.5 | This study§ | Δ(speAspeB) ΔspeC Δ(speDspeE) | ¶ | ¶ |
HT551 | 14 | Δ(speDspeE) | 12 | 0‡ |
speA, arginine decarboxylase; speB, agmatine ureohydrolase; speC, ornithine decarboxylase; speD, S-adenosylmethionine decarboxylase; speE, spermidine synthase (putrescine aminopropyltransferase).
The cells used for these assays were grown in polyamine-deficient VB medium to an OD600 of 0.4–0.5, collected by centrifugation, and extracted with 5% trichloroacetic acid. The supernatant was assayed for putrescine and spermidine by HPLC chromatography (14).
Not detected by HPLC analysis.
JI171, an E. coli strain containing pDT1.5 overexpressing E. coli Mn-SOD (sodA) (6), was kindly provided by J. Imlay (University of Illinois, Urbana). Plasmid DNA was isolated and used to transform EWH319 with standard procedures.
Not determined.