Total Starch Enzymatic Digestion v1

Author(s):  
Lynn Doran ◽  
Amanda P. De Souza

Enzymatic digestion of total soluble starch to glucose in plant tissue extracts for preparation for quantification via the GOD-POD Method (NZYtech).

2021 ◽  
Author(s):  
Lynn Doran ◽  
Amanda P. De Souza

Quantification of total soluble sugars (as glucose) in plant tissue extracts via the sulfuric phenol method adapted for 96 well plates.


1986 ◽  
Vol 69 (1) ◽  
pp. 162-166
Author(s):  
Khaja Khaleeluddin ◽  
Linda Bradford

Abstract Total nonstructural carbohydrates (TNC) in plant tissue are underestimated by single enzyme (a-amylase or glucoamylase) extraction and overestimated by mild acid hydrolysis. A combination of glucoamylase and mycolase degraded starch completely to glucose at 60°C and pH 4.9. This dual enzyme extraction procedure was effective in determining TNC in plant tissues that do not accumulate fructosans. The reducing sugar (mainly glucose and/or fructose) extracts produced by enzymatic digestion of plant tissue were clarified with barium hydroxide and zinc sulfate solutions and analyzed by the Shaffer-Somogyi copperiodometric titration method. The dual enzyme method hydrolyzed pure starch derived from corn, wheat, and potato, and potato-soluble starch to about 100% glucose, whereas mycolase only yielded about 88% hydrolysis. Although corn starch was completely hydrolyzed in 2 h by the dual enzyme method, plant tissues required at least 24 h hydrolysis for maximum TNC values. Lead acetate precipitation of the protein in the dual enzyme extracts interfered with the copper-iodometric titration. Gelatinization of starch in plant tissue by autoclaving gave higher TNC values than heating on a hot plate for 5 min. The Schaffer-Somogyi copper iodometric titration method could be used to measure/or define the activity of certain enzymes.


1990 ◽  
Vol 21 (13-16) ◽  
pp. 1519-1529 ◽  
Author(s):  
R.M. Carlson ◽  
R.I. Cabrera ◽  
J.L. Paul ◽  
J. Quick ◽  
R.Y. Evans

1980 ◽  
Vol 26 (7) ◽  
pp. 807-811 ◽  
Author(s):  
C. H. Liao ◽  
T. A. Chen

Plant tissue extracts prepared from corn, periwinkle, celery, and lettuce contain substance(s) which are inhibitory for spiroplasma growth in culture media. The inhibition titer, measured as the highest dilution of plant extracts which block spiroplasma growth, is inversely proportional to the spiroplasma concentration used for testing. At a concentration of 104 cells/mL, the growth of four spiroplasma isolates investigated (corn stunt spiroplasma, Spiroplasma citri, honey bee spiroplasma, and Bermuda grass (Cynodon dactylon) spiroplasma) was suppressed by the addition of corn and periwinkle extracts up to dilutions of 1/160 and 1/1280, respectively. Spiroplasmas remained viable in extract-supplemented media for at least 5 days and continued to multiply shortly after the plant extract was removed. These results suggest that (1) the inhibitory action of plant extracts is spiroplasmastatic, and (2) inhibitory factors may temporarily bind to cytoplasmic membrane and subsequently suppress the process of cell replication. The anti-mycoplasma activity was greatly reduced when the extract was placed in boiling water for 10 min or at 37 °C for 5 days. No loss of activity was detected when the extract was kept at −20 or 4 °C for 5 days.


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