Analysis of stress responses in the cyanobacterial strains Synechococcus sp. PCC 7942, Synechocystis sp. PCC 6803, and Synechococcus sp. PCC 7418: Osmolyte accumulation and stress protein synthesis

Citation
S. Fulda et al., Analysis of stress responses in the cyanobacterial strains Synechococcus sp. PCC 7942, Synechocystis sp. PCC 6803, and Synechococcus sp. PCC 7418: Osmolyte accumulation and stress protein synthesis, J PLANT PHY, 154(2), 1999, pp. 240-249
Citations number
35
Categorie Soggetti
Plant Sciences","Animal & Plant Sciences
Journal title
JOURNAL OF PLANT PHYSIOLOGY
ISSN journal
01761617 → ACNP
Volume
154
Issue
2
Year of publication
1999
Pages
240 - 249
Database
ISI
SICI code
0176-1617(199902)154:2<240:AOSRIT>2.0.ZU;2-N
Abstract
The influence of salt, hear and light shock treatments on physiological pro cesses was compared in the cyanobacteria Synechococcus sp. PCC 7942, Synech ocystis sp. PCC 6803, and Synechococcus sp. PCC 7418, which differ regardin g their salt tolerance. The accumulation of the osmolytes sucrose and gluco sylglycerol started after salt shocks without a lag in the strains 7942 and 6803. In strain 7418 the synthesis of glycine-betaine showed a lag phase o f several hours. During this time glucosylglycerol and proline were accumul ated. Light shocks led in all strains to the highest reduction of carbon fi xation rate followed by salt shock, while heat shocks decreased it only sli ghtly in the strains 6803 and 7418. Protein synthesis rates measured S-35-m ethionine incorporation were reduced after a salt shock, remained almost un changed in light- as shocked cells and increased after heat shocks. Compari sons of protein synthesis patterns showed that most of the detected stress proteins seem to be strain-specific and belong to the group of general stre ss proteins, since they were induced under heat, salt and light stress trea tments, respectively. Furthermore, some proteins specific for salt and heat stress were also found. Among the general stress proteins the chaperone Dn aK was identified using cross reactions with a specific antibody.