Phytase and acid phosphatase activities in extracts from roots of temperate pasture grass and legume seedlings

1999 ◽  
Vol 26 (8) ◽  
pp. 801 ◽  
Author(s):  
Julie E. Hayes ◽  
Alan E. Richardson ◽  
Richard J. Simpson

Phytase and acid phosphatase activities were measured in extracts from roots of 14- to 22- day old seedlings of a range of temperate pasture species that were grown aseptically in sand culture. Phytase activity from roots of phosphorus- (P-)-deficient Trifolium subterraneum L. was characterised. Activity was enhanced by 40% when extracts were passed through Sephadex G-25, and increased by a further 20–30% with the addition of either 1 mМ EDTA or 5 mМ cysteine to assay solutions. The optimum temperature for phytase activity was 50°C and the optimum pH was 5.3. When compared with phosphatase activity measured in the roots of T. subterraneum, phytase activity exhibited narrower pH and temperature optima, and was also more strongly inhibited by Co2+, Zn2+ and AsO42− ions. Significantly, for the five pasture species examined, phytase activity was less than 5% of the total acid phosphatase activity in extracts of plant roots. Measured phytase activity ranged between 0.13 and 1.7 nkat g–1 root fresh wt and was enhanced under P-deficient relative to P-sufficient growth conditions in all of the pasture species with the exception of Trifolium repens L., for which the Km constant for activity was 50% lower in P-deficient plants. When expressed on a root fresh wt basis, increases in phytase activity of ~1.25-fold were observed for extracts from T. subterraneum and Medicago polymorpha L., and of up to 3.3-fold for Danthonia richardsonii A.B. Cashmore and Phalaris aquatica L. Increases in acid phosphatase activity with P deficiency were less evident. Between 3.1% and 4.3% only of the total phytase activity measured in root extracts was eluted from intact roots into 0.1 М NaCl.

1972 ◽  
Vol 18 (8) ◽  
pp. 841-844 ◽  
Author(s):  
Diane L Fabiny-Byrd ◽  
Gerhard Ertingshausen

Abstract Acid phosphatase activity is determined by splitting 1-naphthyl phosphate, concurrently diazotizing the released 1-naphthol with Fast Red TR, and measuring the resulting color. The test is performed in the presence and absence of tartrate. Reaction rates can be continuously monitored, and their difference is proportional to acid phosphatase activity that is inhibited by tartrate. Results for sera with normal and increased acid phosphatase activities are presented and three different methods for acid phosphatase are compared. The kinetic blank used in the reaction eliminates all nonenzymatic contributions to substrate splitting.


2000 ◽  
Vol 80 (1) ◽  
pp. 91-97 ◽  
Author(s):  
B. Gagnon ◽  
R. Lalande ◽  
R. R. Simard ◽  
M. Roy

Combined primary and secondary papermill sludge (PS) is a good source of C and other nutrients for soils devoted to intensive horticultural production. A field study was conducted to evaluate the effect of PS, spring-applied alone or in combination with ammonium nitrate (AN), on the enzymatic activity of a Bedford clay (Humic Gleysol) in the province of Québec, Canada. The experiment was started in 1996 with winter cabbage (Brassica oleracea var. capitata L.) and continued in 1997 and 1998 on the same plots with sweet corn (Zea mays L.). The PS was applied at 0 (control), 8, 16, 32 and 65 Mg ha−1 in 1996 and at 44% of these rates in 1997. No sludge was applied in 1998. Additional treatments consisted of AN applied yearly at 100% of the plant N requirements and a PS and AN combination. Soil arylsulfatase and acid and alkaline phosphatase activities were measured at three different times in each growing season. The PS rate linearly increased the soil acid phosphatase activity in all 3 yr. In contrast, the alkaline phosphatase and arylsulfatase activities were enhanced in 1997 by the 8–16 Mg PS ha−1 treatments, whereas larger amounts of PS showed activity comparable to the control. The second PS application promoted phosphatase activities mostly in fall, but did not sustain arylsulfatase activity. The AN gave lower phosphatase activities than PS, and depressed arylsulfatase. Addition of AN to PS increased only acid phosphatase activity as compared with PS alone or the control. This study indicated that addition of PS improved enzyme activity of this horticultural soil but rates in excess to 32 Mg ha−1 may be detrimental. Key words: Papermill sludge, soil enzyme, cabbage, corn


1970 ◽  
Vol 47 (2) ◽  
pp. 167-176 ◽  
Author(s):  
JEANNE A. SMITH ◽  
H. B. WAYNFORTH

SUMMARY Free and total acid phosphatase activity has been measured in individual corpora lutea from rat ovaries in various reproductive states (both natural and experimentally induced). Significant changes both in weight and enzymic activity were found, and an attempt has been made to correlate these with the growth and regression of the corpora lutea. A possible connexion between acid phosphatase activity, progesterone secretion and/or cellular composition of the corpus luteum is suggested.


1986 ◽  
Vol 235 (2) ◽  
pp. 351-357 ◽  
Author(s):  
M F Lin ◽  
G M Clinton

The major secreted isoenzyme of human prostatic acid phosphatase (PAcP) (EC 3.1.3.2), which catalyses p-nitrophenyl phosphate (PNPP) hydrolysis at acid pH values, was found to have phosphotyrosyl protein phosphatase activity since it dephosphorylated three different phosphotyrosine-containing protein substrates. Several lines of evidence are presented to show that the phosphotyrosyl phosphatase and PAcP are the same enzyme. A highly purified PAcP enzyme preparation which contains a single N-terminal peptide sequence was used to test for the phosphotyrosyl phosphatase activity. Both activities comigrated during gel filtration by high performance liquid chromatography. Phosphotyrosyl phosphatase activity and PNPP acid phosphatase activity exhibited similar sensitivities to different effectors. Both phosphatase activities showed the same thermal stability. Specific anti-PAcP antibody reacted to the same extent with both phosphatase activities. PNPP acid phosphatase activity was competitively inhibited by the phosphotyrosyl phosphatase substrate. To characterize further the phosphotyrosyl phosphatase activity, the Km values using different phosphoprotein substrates were determined. The apparent Km values for phosphorylated angiotensin II, anti-pp60src immunoglobulin G and casein were in the nM range for phosphotyrosine residues, which was about 50-fold lower than the Km for phosphoserine residues in casein.


1970 ◽  
Vol 18 (7) ◽  
pp. 473-481 ◽  
Author(s):  
C. Y. LI ◽  
L. T. YAM ◽  
K. W. LAM

Acid phosphatase in human leukocytes was examined in a large number of patients with a variety of hematologic diseases. In chronic lymphocytic leukemia the total leukocyte acid phosphatase activity was markedly decreased. This was due to the drastic increase of enzyme-poor leukemic lymphocytes and the concomitant decrease of enzyme-rich monocytes and neutrophils. Further examination by disc gel electrophoresis revealed that the leukocytes in this disease contained only one of the five acid phosphatase isoenzymes present in a normal leukocyte preparation. Total acid phosphatase activity was not significantly altered in other hematologic disorders, yet different ratios of the isoenzymes shown by disc gel electrophoresis were observed in Hodgkin's disease, chronic granulocytic leukemia, acute granulocytic leukemia, infectious mononucleosis and leukemic reticuloendotheliosis.


Parasitology ◽  
1980 ◽  
Vol 80 (1) ◽  
pp. 23-38 ◽  
Author(s):  
Jun Maki ◽  
Toshio Yanagisawa

SummaryAcid phosphatase activity was demonstrated in the intact blood nematodes, Dirofilaria immitis and Angiostrongylus cantonensis. Biochemical studies on acid phosphatase, using intact females and whole worm, body-wall and visceral homogenates were undertaken to clarify the characteristics and the distribution of the enzyme. In D. immitis, high acid phosphatase activity was observed at pH 3·8–5·8 and in A. cantonensis, at pH 4·5–6·0. Molybdate, fluoride, copper and zinc ions and L(+)-tartrate were effective inhibitors of the enzymes of both parasites while cobalt and magnesium ions and D(−)-tartrate had no noticeable effect on the activity. When the effect of substrate concentration on the phosphatase activity was studied, kinetic curves of Michaelis–Menten type were obtained with the 2 species of intact worms as well as their homogenates. The reproductive organs and body wall of D. immitis showed high total acid phosphatase activity. In A. cantonensis, the majority of the enzyme was localized in the body wall. The activity of intact A. cantonensis expressed as μg Pi/h/mg dry weight decreased with increase in mean worm weight. The characteristics of the acid phosphatase of the 2 nematodes are compared with those of other parasitic helminths and of acid phosphatase of mammalian origin. The localization of the phosphatase responsible for the hydrolysis of the external substrate has been discussed for D. immitis and A. cantonensis based on results of the kinetics and distribution of the enzyme.


1995 ◽  
Vol 41 (2) ◽  
pp. 200-203 ◽  
Author(s):  
S Osawa ◽  
S Iida ◽  
H Yonemitsu ◽  
K Kuroiwa ◽  
K Katayama ◽  
...  

Abstract We characterized six self-indicating substrates, synthesized as the derivative compounds of acetylphenyl phosphate, for serum prostatic acid phosphatase (PAP) activity. One of the substrates, 2,6-dichloro-4-acetylphenyl phosphate (DCAPP), is superior to others in terms of stability, affinity, and low Km for PAP. The hydrolyzed product, 2,6-dichloro-4-acetylphenol (DCAP), has a maximum absorption at 334.2 nm, a pKa of 4.15, and a molar absorptivity at 340 nm of 21,490 L.mol-1.cm-1 in citrate-HCl buffer, pH 5.4. PAP activity was assessed by subtracting tartaric acid-inhibited acid phosphatase activity from total acid phosphatase activity. Our assay system involving DCAPP is a unique kinetic method that shows good reproducibility, wide analytical dynamic range, and high specificity for PAP. Moreover, it is easily adaptable to automated analyzers because the product, DCAP, can be monitored at 340 nm.


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