4395487 method for assay of alpha-amylase activity

1
340 PATENT ABSTRACTS range, and little sensitivity to heavy metal ion in- hibition. The enzyme may be immobilized on an organic macroporous polymer or in an alginate gel. 4396602 BLOOD GLUCOSE LEVEL LOWERING AGENTS Akira Endo. Tokyo, Japan assigned to Asahi Kasei Kogyo Kabushiki Kaisha A method of lowering the blood glucose level in mammals and a blood glucose level-lowering a- gent are described. The method comprises ad- ministering an enzyme capable of synthesizing sparingly-digestible saccharides from easily- digestible saccharides. The blood glucose level- lowering agent comprises the enzyme capable of synthesizing sparingly-digestible saccharides from easily-digestible saccharides and a glucosidase-inhibiting agent. 4395487 METHOD FOR ASSAY OF ALPHA-AMYLASE ACTIVITY Narimas Saito, Tatsuo Horiuchi, Noda, Japan assigned to Noda Institute for Scientific Research A method for the assay of alpha-amylase ac- tivity, which compriSeS adding an alpha- amylase-containing sample to maltohexaitol or maltohexaonic acid used as substrate, reacting, at the same time or subsequent to the addition, alpha-glucosidase with the resulting mixture, and determining the reaction product to assay the alpha-amylase activity. 4394450 METHOD FOR PURIFICATION OF URICASE David A Brock, Surendra K Gupta assigned to Miles Laboratories Inc A method is provided for purifying uricase by decreasing the amount of active catalase present. The method involves adjusting the pH of a catalase-containing uricase preparation to a pH in the range of about I I to 13 to inactivate the catalase and recovering a uricase preparation substantially free of active catalase. 4394449 STABILIZATION OF COENZYMES IN AQUEOUS SOLUTION Ivan E Modrovich A stabilized aqueous coenzyme solution is dis- closed for use in the clinical assay of a selected biological constituent through the enzymic reac- tion of an enzyme with a selective substrate for the enzyme and a coenzyme. The aqueous coen- zyme solution comprises at least one first enzyme and a first substrate for selectively reacting with the fir.st enzyme in the assay, a coenzyme for interacting with the first enzyme and first subs- trate in the assay which coenzyme degrades for- ming a coenzyme conversion product, and at least one second enzyme and second substrate selective for the second enzyme which react with the coenzyme conversion product to regenerate the coenzyme. 4394445 ENZYMATIC GLYCERIDE HYDROLYSIS Paul T Nix, Janet M Santoro, Joyce E Stephens A new stable combination of Rhizopus arrhizus lipase and Pseudomonas fluorescens lipase for

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Page 1: 4395487 Method for assay of alpha-amylase activity

340 PATENT ABSTRACTS

range, and little sensitivity to heavy metal ion in- hibition. The enzyme may be immobilized on an organic macroporous polymer or in an alginate gel.

4396602

B L O O D G L U C O S E L E V E L L O W E R I N G A G E N T S

Akira Endo. Tokyo, Japan assigned to Asahi Kasei Kogyo Kabushiki Kaisha

A method of lowering the blood glucose level in mammals and a blood glucose level-lowering a- gent are described. The method comprises ad- ministering an enzyme capable of synthesizing sparingly-digestible saccharides from easily- digestible saccharides. The blood glucose level- lowering agent comprises the enzyme capable of synthesizing sparingly-digestible saccharides from easily-digestible saccharides and a glucosidase-inhibiting agent.

4395487

M E T H O D F O R A S S A Y O F A L P H A - A M Y L A S E A C T I V I T Y

Narimas Saito, Tatsuo Horiuchi, Noda, Japan assigned to Noda Institute for Scientific Research

A method for the assay of alpha-amylase ac- tivity, which compriSeS adding an alpha- amylase-containing sample to maltohexaitol or maltohexaonic acid used as substrate, reacting, at the same time or subsequent to the addition, alpha-glucosidase with the resulting mixture, and determining the reaction product to assay the alpha-amylase activity.

4394450

M E T H O D F O R P U R I F I C A T I O N O F U R I C A S E

David A Brock, Surendra K Gupta assigned to Miles Laboratories Inc

A method is provided for purifying uricase by decreasing the amount of active catalase present. The method involves adjusting the pH of a catalase-containing uricase preparation to a pH in the range of about I I to 13 to inactivate the catalase and recovering a uricase preparation substantially free of active catalase.

4394449

S T A B I L I Z A T I O N O F C O E N Z Y M E S I N A Q U E O U S

S O L U T I O N

Ivan E Modrovich

A stabilized aqueous coenzyme solution is dis- closed for use in the clinical assay of a selected biological constituent through the enzymic reac- tion of an enzyme with a selective substrate for the enzyme and a coenzyme. The aqueous coen- zyme solution comprises at least one first enzyme and a first substrate for selectively reacting with the fir.st enzyme in the assay, a coenzyme for interacting with the first enzyme and first subs- trate in the assay which coenzyme degrades for- ming a coenzyme conversion product, and at least one second enzyme and second substrate selective for the second enzyme which react with the coenzyme conversion product to regenerate the coenzyme.

4394445

E N Z Y M A T I C G L Y C E R I D E H Y D R O L Y S I S

Paul T Nix, Janet M Santoro, Joyce E Stephens

A new stable combination of Rhizopus arrhizus lipase and Pseudomonas fluorescens lipase for