1973
DOI: 10.1099/00221287-79-2-233
|View full text |Cite
|
Sign up to set email alerts
|

A New Medium for the Isolation and Growth of Auxotrophic Mutants of the Blue-green Alga Anacystis nidulans

Abstract: A complete medium of defined composition has been developed for quantitative growth of wild-type and auxotrophic mutant strains of Anacystis nidulans. This medium has proved to be more satisfactory than other complex media (for example casein hydrolysate, yeast extract) for both the isolation and the growth of auxotrophs. Rigorous control of the pH of complete and other supplemented media is essential for quantitative growth on agar. Four diagnostic media are described which each contain a different combinatio… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

0
40
0

Year Published

1981
1981
1999
1999

Publication Types

Select...
6
4

Relationship

0
10

Authors

Journals

citations
Cited by 90 publications
(40 citation statements)
references
References 9 publications
0
40
0
Order By: Relevance
“…[20] with twice the concentration of nitrate. For the solid medium, 1.5°70 agar autoclaved separately was added.…”
Section: Growth Conditionsmentioning
confidence: 99%
“…[20] with twice the concentration of nitrate. For the solid medium, 1.5°70 agar autoclaved separately was added.…”
Section: Growth Conditionsmentioning
confidence: 99%
“…Cells were maintained axenically on 1.4% agar slants made with Allen's medium (1) and kept under low light (15 uE m-2 s-') provided by a combination of warm white and Gro-lux fluorescent lamps (Sylvania, Canada). Single cell isolates, obtained by dilution plating on the minimal medium of Herdman et al (15), were used in all studies.…”
Section: Methodsmentioning
confidence: 99%
“…strain PCC 6803 was grown photoautotrophically under continuous fluorescent illumination (25 W. m -2, white light) at 35°C on a synthetic medium [6] Glutamate dehydrogenase aminating activity was determined at 30°C in a reaction mixture containing 85 mM Tris-HC1 buffer (pH 8.0), 10 mM 2-oxoglutarate, 50 mM NH4CI and 0.2 mM NADPH. The reaction was started by addition of ammonium chloride and followed either spectrophotometrically at 340 nm or by glutamate formation.…”
Section: Growth Of Cellsmentioning
confidence: 99%