TY - JOUR
T1 - S‐Adenosylhomocysteine Hydrolase Deficiency in Cysteine Auxotrophs of Tetrahymena thermophila
AU - Murphy, Sharon E.
AU - Fall, Ray
N1 - Copyright:
Copyright 2016 Elsevier B.V., All rights reserved.
PY - 1985/2
Y1 - 1985/2
N2 - The biochemical lesion in two cysteine auxotrophs of Tetrahymena thermophila has been established as a defect in S‐adenosylhomocysteine hydrolase, an enzyme of the transsulfuration pathway. As a result, these mutants require cysteine (or cystathionine or homocysteine) for growth in a denned medium. Cell‐free extracts of the mutants contained < 5% of the level of the enzyme seen in the wild type. One of the mutant strains accumulated intracellular levels of S‐adenosylhomocysteine as high as 1380 üM, a level 200 times normal. When both mutant strains were maintained in defined medium without cysteine, growth occurred after a long lag; this phenomenon was termed “adaptation.” Adaptation was a) reversed by passage through rich medium, b) was not a recovery of S‐adenosylhomocysteine hydrolase, and c) was probably linked to induction of an alternate pathway for cysteine biosynthesis, involving a lysosomal S‐adenosylhomocysteine nucleosidase activity.
AB - The biochemical lesion in two cysteine auxotrophs of Tetrahymena thermophila has been established as a defect in S‐adenosylhomocysteine hydrolase, an enzyme of the transsulfuration pathway. As a result, these mutants require cysteine (or cystathionine or homocysteine) for growth in a denned medium. Cell‐free extracts of the mutants contained < 5% of the level of the enzyme seen in the wild type. One of the mutant strains accumulated intracellular levels of S‐adenosylhomocysteine as high as 1380 üM, a level 200 times normal. When both mutant strains were maintained in defined medium without cysteine, growth occurred after a long lag; this phenomenon was termed “adaptation.” Adaptation was a) reversed by passage through rich medium, b) was not a recovery of S‐adenosylhomocysteine hydrolase, and c) was probably linked to induction of an alternate pathway for cysteine biosynthesis, involving a lysosomal S‐adenosylhomocysteine nucleosidase activity.
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U2 - 10.1111/j.1550-7408.1985.tb03009.x
DO - 10.1111/j.1550-7408.1985.tb03009.x
M3 - Article
C2 - 3989751
AN - SCOPUS:0022021943
SN - 1066-5234
VL - 32
SP - 32
EP - 37
JO - Journal of Protozoology
JF - Journal of Protozoology
IS - 1
ER -