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Literature summary for 3.2.1.B26 extracted from

  • Haseltine, C.; Montalvo-Rodriguez, R.; Bini, E.; Carl, A.; Blum, P.
    Coordinate transcriptional control in the hyperthermophilic archaeon Sulfolobus solfataricus (1999), J. Bacteriol., 181, 3920-3927.
    View publication on PubMedView publication on EuropePMC
Search for more literature for 3.2.1.B26

Cloned(Commentary)

Cloned (Comment) Organism
expression in Escherichia coli Saccharolobus solfataricus

Organism

Organism UniProt Comment Textmining
Saccharolobus solfataricus P22498
-
-
Saccharolobus solfataricus P2 P22498
-
-

Purification (Commentary)

Purification (Comment) Organism
-
 Saccharolobus solfataricus

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
4-nitrophenyl beta-D-glucopyranoside + H2O
-
 Saccharolobus solfataricus 4-nitrophenol + D-glucose
-
 ?
4-nitrophenyl beta-D-glucopyranoside + H2O
-
 Saccharolobus solfataricus P2 4-nitrophenol + D-glucose
-
 ?

Synonyms

Synonyms Comment Organism
LACS
-
 Saccharolobus solfataricus

Expression

Organism Comment Expression
Saccharolobus solfataricus levels of lacS mRNA are reduced 20fold as a consequence of yeast extract medium supplementation to sucrose minimal medium. A passive mechanism involving cell dilution is used to repress lacS expression down
Saccharolobus solfataricus induction when cells which were maintained in sucrose minimal medium with yeast extract are down shifted to sucrose minimal medium without yeast extract addtion. An increase is evident after 2 h of incubation and reaches maximum levels 6 h after the shift. An active mechanism is employed for induction of lacS expression. Levels of lacS mRNA are reduced 20fold as a consequence of yeast extract medium supplementation to sucrose minimal medium. A passive mechanism involving cell dilution is used to repress lacS expression up