scholarly journals Fungal Cellulases XX. Some Observations on the Induction and Inhibition of the Cellobiase of Stachybotrys Atra

1967 ◽  
Vol 20 (1) ◽  
pp. 193 ◽  
Author(s):  
MA Jermyn

The induction of cellobiase in washed suspensions of Stachybotrys atra mycelium harvested during the active phase of growth follows the classical pattern for induced protein synthesis, except that it does not appear to be dependent on continued growth of the organism. At 28�C under aerobic conditions there is no detectable lag period. Inducers are ,B.glucosides of polyhydroxylic aglycones, which may be another sugar residue or a chain of such residues. Such inducers are metabolizable by the mould; after their breakdown the enzyme rapidly disappears from the mycelium. Interference with RNA metabolism and information transfer depresses the induced synthesis of the enzyme; two amino acid analogues, ,B-chloroalanine and p-fiuorophenylalanine, also inhibit this induction. Inhibition is also observed when respirable substances are present, and the inhibitor appears to arise from the metabolism of pyruvate.

1971 ◽  
Vol 9 (3) ◽  
pp. 679-699
Author(s):  
D. R. SOLL ◽  
D. R. SONNEBORN

1. Zoospores germinate rapidly and semi-synchronously upon exposure to growth medium or an inorganic salts solution. Amino acid incorporation into protein is detected only after a characteristic lag period, the extent of which is a function of developmental, rather than absolute, time. 2. The ‘turn-on’ of amino acid incorporation occurs after several of the morphological events of germination have taken place - notably, retraction of the flagellum, conversion to a spheroid cell morphology, vesicle fusion with the plasma membrane, formation of the initial cell wall, and elongation of the single mitochondrion. A second group of morphological changes - release of ribosomes from the nuclear cap into the cytoplasm, appearance of multiple mitochondrial profiles, disappearance of the flagellar axoneme, and disappearance of gamma particles - takes place in the cell population during the turn-on of incorporation. 3. Cycloheximide reversibly inhibits germination at a characteristic block point. Inhibited cells accomplish all the known morphological events of germination except the disappearance of the flagellar axoneme and the formation of the germ tube. Amino acid incorporation is inhibited to undetectable levels in growth medium and by about 80% in the inorganic salts medium. Nevertheless, the population kinetics for the morphological changes which occur in cycloheximide-inhibited cells are indistinguishable from those in untreated cells. Cycloheximide effectively enters cells prior to the characteristic block point, since the drug drastically inhibits the low level of amino acid incorporation by zoospores. 4. ‘Pools’ extractable by trichloroacetic acid (TCA) have been examined; the results do not support the possibility of extensive early protein synthesis from endogenous sources. 5. Actinomycin D, at levels which inhibit [3H]uridine incorporation into TCA-precipitable material (nucleic acid) by over 98%, does not affect the population kinetics of germination. The drug does not affect the lag period for amino acid incorporation. The rate of amino acid incorporation (pulse labelling) fluctuates predictably during germination. Actinomycin D only partially inhibits the first ‘round’ of incorporation, but severely inhibits the second. From this information, we conclude that: (a) the proteins necessary for most of the structural events of germination are preformed in the zoospore; (b) therefore, these events are controlled directly by mechanisms other than differential protein synthesis; (c) two of the known events - disappearance of the flagellar axoneme and formation of the germ tube - do appear to have a requirement for concomitant protein synthesis; (d) germination does not require de novo RNA synthesis; and (e) certain of the first proteins made during germination are evidently synthesized with preformed messages.


1960 ◽  
Vol 5 (4) ◽  
pp. 207-216 ◽  
Author(s):  
J. Janeček ◽  
J. Chaloupka ◽  
K. Vereš ◽  
M. Havbánek

1971 ◽  
Vol 125 (3) ◽  
pp. 751-756 ◽  
Author(s):  
R. C. Hider ◽  
E. B. Fern ◽  
D. R. London

1. The effects of insulin in vitro on tissue pools and incorporation into protein of glycine and leucine in the extensor digitorum longus muscle of the rat are reported. 2. It was found that insulin decreased the lag period before the establishment of a linear rate of incorporation of radioactive glycine into protein. 3. The hormone increased the size of the free intracellular glycine pool. No such effect was found for leucine. The accumulation of radioactive glycine in the intracellular fluid compartment was increased. The content of radioactive leucine in the intracellular compartment was decreased. 4. Insulin decreased the specific radioactivity of both glycine and leucine in the extracellular fluid. 5. The hormone also decreased protein catabolism. 6. The effect on protein synthesis was not caused by an increase in the specific radioactivity of the extracellular pool but was possibly related to increased amino acid concentrations in this pool, which could in turn have affected the aggregation of ribosomes.


1967 ◽  
Vol 20 (1) ◽  
pp. 221 ◽  
Author(s):  
MA Jermyn

The use of Modocoll M (ethyl hydroxyethyl cellulose) as a soluble inducing agent for the cellulase of Stachybotrys atra is described. Some characteristics both of the kinetics of the induction and its inhibition have been determined. There is a lag period of 2�5 hr in the induction at 28�C for peptone-grown mycelium, and added sugars appear to be competitive with the inducer. These two characteristics have previously been noted as peculiarities in the induction of aryl ,a-glucosidase. The induction is also dependent on the continued presence of long-chain polymer. Inhibition experiments suggest that the normal processes of induced protein synthesis are operating in all other particulars, although the details of this inhibition are different from those observed in cellobiase induction. The way in which cellobiase and cellulase induction may be integrated during natural growth on cellulose is discussed.


2000 ◽  
Author(s):  
Anne K. Kowal ◽  
Caroline Kohrer ◽  
Uttam L. RajBhandary

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