IES20040848A2 - Assay for detmination of free D-glactose and/or L-arabinose - Google Patents

Abstract

The invention provides an assay kit for the measurement of free D-galactose and/or L-arabinose in a sample, the kit comprising galactose mutarotase and beta-galactose dehydrogenase. The kit may further comprise a reagent capable of hydrolysing molecules containing D-galactose and/or L-arabinose, to yield the free mono- or di-saccharide so that the kit finds use for determinatin of not just of free D-galactose and/or L-arabinose but also those molecules as released (or synthesized) from other molecules, including lactose, D-galacose-1-phosphate, galactosy1-sucrose oligosaccharides (such as raffinose), galacan, galactomannan, arabinan and arabinogalactan.

Description

Title Assay for determination of free D-galactose and/or L-arabinose Field of the Invention The present invention relates to an improved and rapid assay for the determination of Dgalactose and L-arabinose. In particular the assay of the invention may be used to assay free D-galactose and free L-arabinose or these monosaccharides as released (or synthesized) from other molecules, such as lactose, D-galacose-1-phosphate, galactosylsucrose oligosaccharides (such as raffinose), galactan, galactomannan, arabinan and arabinogalactan.

Brief Background of Invention OPEN TO PUBLIC INSPECTION UNDER SECTION 28 AND RULE 23 JKl Hi. 2£££._ of i Ζ.0ΛΟ6 Lactose, or milk sugar, is a white crystalline disaccharide. It is formed in the mammary glands of all lactating animals and is present in their milk. Lactose yields D-galactose and D-glucose on hydrolysis by lactase (β-galactosidase), an enzyme found in gastric juice. People who lack this enzyme after childhood cannot digest milk and are said to be lactose intolerant. Common symptoms of lactose intolerance include nausea, cramps, gas and diarrhea, which begin about 30 minutes to 2 hours after eating or drinking foods containing lactose. Between 30 and 50 million Americans are lactose intolerant. Certain ethnic and racial populations are more widely affected than others. As many as 75 percent of all African-Americans and Native Americans and 90 percent of Asian-Americans are lactose intolerant. The condition is least common among persons of northern European descent. There is thus a need in the food and beverage industry to be able to rapidly and accurately measure lactose levels.

Galactos(a)emia, characterised by the deficiency of one or more enzymes required by an infant to metabolise D-galactose, is a serious and potentially life-threatening disease. If IE 04 0 8 48 undiagnosed, D-galactose rapidly builds-up in the blood of newborn babies, and can cause cataracts, growth and mental retardation, liver damage and even death. The occurrence of Galactos(a)emia is approximately 1 in 20,000, and tests for the condition form part of a panel of assays performed as part of newborn screening programs. There are two types of enzymatic test used for the diagnosis of Galactos(a)emia; the first is designed to identify the deficiency of galactose-1-phosphate uridyltransferase, the predominant cause of the condition, and the second quantifies total blood D-galactose (comprising free D-galactose and that in the form of D-galactose-1-phosphate), thus identifying Galactos(a)emia regardless of the cause. Once diagnosed, a sucrose based milk formula free of lactose ensures healthy development of the child. There is thus an established and appreciated requirement to rapidly and accurately determine D-galactose in the clinical environment.

Arabinose finds applications in the flavour, food and pharmaceutical industries, for example in controlled Maillard reactions, as a sweetener, and when derivatised as an antiviral agent, respectively. As L-arabinose is one of the most abundant pentoses on earth, much research activity is focused on the di-, oligo- and polysaccharides that contain this monosaccharide, such as arabinooligosaccharides, arabinoxylans, arabinogalactans and arabinans. Thus, there is a general requirement for a simple and rapid test for L-arabinose. Similarly, much research is performed on di-, oligo- and polysaccharides containing D-galactose, such as galactosyl-sucrose oligosaccharides (such as raffinose), galactooligosaccharides, galactans, galactomannans, arabinogalactans, and glycoforms of glycoproteins, and thus there is also a requirement for a simple and rapid test for D-galactose in this area.

There is a large and well established market for the enzymatic determination of free Dgalactose and D-galactose as released from lactose, especially in milk and dairy products, but also in many other foodstuffs and materials. Enzymatic methods for the measurement of lactose are well known and are generally based on the hydrolysis of lactose to Dglucose and D-galactose with β-galactosidase followed by determination of either IE 0 4 0 8 4 8 D-galactose or D-glucose. Quantification by measurement of the released D-galactose is greatly preferred, as foodstuffs in general contain much higher levels of free D-glucose than free D-galactose. However, due to an inherent rate limiting factor fundamental to the biochemistry employed, all current products are very slow, taking between 20 and 40 minutes to complete, and optimally require incubation at a high temperature of approximately 40°C, as compared to the optimal time expected/preferred by the modem analyst of between 2 and 5 minutes (and at ambient room temperature).

The fundamentals of the currently employed methods for the measurement of free Dgalactose and D-galactose as released from lactose and earlier citations can be found in Beutler, H. -O. (1988). Lactose and D-Galactose. In Methods of Enzymatic Analysis (Bergmeyer, H. U., ed.), 3rd ed., Vol.VI, pp. 104-112, VCH Publishers (UK) Ltd, Cambridge, UK. Those for the measurement of free L-arabinose can be found in Sturgeon R. J. (1988). L-Arabinose. Also in Methods of Enzymatic Analysis pp. 427-431.

An enzymatic test kit for lactose and D-galactose, based on the existing traditional methodology using just β-galactose dehydrogenase, is currently offered by Megazyme (cat. no. K-LACGA), as well as Boehringer Mannheim GmbH, Roche (via R-biopharm), and Scil Diagnostics GmbH.

Object of the Invention It is thus an object of the invention to provide an assay kit which has a rapid completion time, for the determination of free D-galactose and/or free L-arabinose, or these monosaccharides as released (or synthesized) from other molecules. Those molecules maybe lactose, D-galacose-1 -phosphate, galactosyl-sucrose oligosaccharides (such as raffinose), galactan, galactomannan, arabinan and arabinogalactan and the like.

It is a further object to provide an assay kit for conducting the above assays at room temperature.

IE 04 0 8 4 8 Another object is to provide a cheap and reliable assay kit. A further object is to provide a simple and quantitative assay kit.

In particular it is an object to provide a test kit for the rapid measurement of free Dgalactose and D-galactose as released from lactose, in approximately 5 minutes at room temperature.

A yet further particular object is to provide a test kit for the rapid measurement of free Dgalactose and D-galactose as released from D-galactose-1-phosphate, both as constituents of blood, in particular that of newborn babies, in approximately 5 minutes at room temperature.

Brief Summary of Invention According to the present invention there is provided a test kit for the measurement of free D-galactose and/or L-arabinose comprising galactose mutarotase and β-galactose dehydrogenase.

The assay kit may further comprise NAD+.

The galactose mutarotase may be selected from GalM derived from E. coli, porcine kidney mutarose, or any other mutarotase catalyzing the interconversion of a- and β-Dgalactose and/or a- and β-L-arabinose.

The assay kit may further comprise a reagent capable of releasing D-galactose and/or Larabinose, or in assisting other reagents in releasing D-galactose and/or L-arabinose from larger molecules. The reagent may be an emzyme selected from β-galactosidase, βgalactanase, α-galactosidase, eni/c-arabinanase, e.ro-arabinanase, a-Larabinofuranosidase, acid phosphatase, alkaline phosphatase, β-mannanase, βmannosidase, β-xylanase, α-glucuronidase, esterase, and xylan acetyl-esterase.

IE 04 0 8 48 Preferably the kit further comprises a buffer with or without other chemical additives, in the pH range 4.0 to 10.0. For the higher pH values, the buffer may be Tris/HCl buffer containing EDTA.

Suitably the assay kit comprises sufficient galactose mutarotase to give a concentration of at least 0.1 pg/mL in the final assay mixture. Preferably the concentration is at least 1 pg/mL , more preferably at least 3 pg/mL in the final assay mixture.

The kit is suitable for the determination of D-galactose and L-arabinose. In particular, the kit may be used for the determination of free D-galactose and free L-arabinose or these monosaccharides as released (or synthesized) from other molecules, such as lactose, D-galacose-1-phosphate, galactosyl-sucrose oligosaccharides (such as raffinose), galactan, galactomannan, arabinan and arabinogalactan.

This improvement offers the great advantages of requiring less equipment time and staff costs, and no need for inconvenient high temperature incubations, that require additional or more sophisticated equipment.

Brief Description of the Drawings Figure 1: shows the effect of increasing amounts of β-galactose dehydrogenase in a conventional lactose assay using Megazyme reagents.

Figure 2: shows the effect of increasing amounts of β-galactose dehydrogenase in the presence of 0.02 mL galactose mutarotase in a lactose assay.

Figure 3: shows the effect of varying amounts of Biozyme mutarotase in a SCIL Lactose / D-Galactose Kit using Megazyme standard solution.

Figure 4: shows the effect of varying amounts of Biozyme mutarotase in a Megazyme Lactose / D-Galactose Kit using Megazyme standard solution.

IE 0 4 0 8 4 8 Detailed Description of Invention Example 1 Principle of all Current Products for the Determination of Free DGalactose and/or L-Arabinose All currently available test kits for the determination of free D-galactose and/or Larabinose, or these monosaccharides as released (or synthesized) from other molecules, such as lactose, D-galacose-1-phosphate, galactosyl-sucrose oligosaccharides (such as raffmose), galactan, galactomannan, arabinan and arabinogalactan, are fundamentally the same in terms of reaction biochemistry employed, and contain the following reagents: 1. Buffer at a high pH (e.g. 8.6 with the Megazyme kit) 2. NAD+ 3. β-Galactose dehydrogenase 4. Standard sugar solution . β-Galactosidase 6. Buffer at a low pH (e.g. 4.5 with the Megazyme kit) For instance, the Megazyme kit reagents are supplied in 6 bottles as follows: Bottle 1: Tris/HCl buffer (25 mL, 2 M, pH 8.6) plus EDTA (40 mM) and sodium azide (0.02 % w/v) as a preservative.

Bottle 2: NAD+ (96 mg).

Bottle 3: β-Galactose dehydrogenase suspension in 3.2 M ammonium sulphate (2.4 mL, 100 U/mL).

Bottle 4: Galactose standard solution (5 mL, 0.4 mg/mL in 0.02 % w/v sodium azide).

IE 04 0 8 48 Bottle 5: β-Galactosidase suspension (1.2 mL, 4000 U/mL).

Bottle 6: Sodium acetate buffer (25 mL, 2 M, pH 4.5).

The lactose test procedure, for instance, involves mixing an aliquot of sample solution with the low pH buffer and β-galactosidase. After hydrolysis of the lactose to D-galactose and D-glucose (see equation 1), the pH is increased by addition of the high pH buffer, and then after the addition of NAD+ and β-galactose dehydrogenase, galactonic acid and NADH are formed. As NADH absorbs light at 340 nm whereas NAD+ does not significantly, this wavelength is used to monitor progress of the reaction (see equation 2 and figure 1). The determination must be quantitative if the results are to be meaningful, and thus the analyst must wait until all the free or liberated D-galactose has been fully converted to D-galactonic acid and NADH, i.e. when there is no further absorbance increase at 340 nm (see figure 1). (β-galactosidase) (1) Lactose + H2O -► D-galactose + D-glucose (β-galactose dehydrogenase) (2) β-D-Galactose + NAD+ -► D-galactonic acid + NADH + H+ The currently available commercial enzymatic kits designed primarily for the measurement of free D-galactose and lactose, also enable the quantification of Larabinose, according to equation 3. (β-galactose dehydrogenase) (3) L-Arabinose + NAD+ -► L-arabinonic acid + NADH + H+ IE 04 08 48 Limitations of All Current Products for the Determination of Free D-Galactose and/or L-Arabinose We have discovered that all current methodologies that ultimately measure free Dgalactose and/or L-arabinose, or these monosaccharides as released (or synthesized) from other molecules, such as lactose, D-galacose-1-phosphate, galactosyl-sucrose oligosaccharides (such as raffinose), galactan, galactomannan, arabinan and arabinogalactan, with NAD+ and β-galactose dehydrogenase, are severely limited by the fact that the rate determining step of approach to the endpoint of the reaction is formation of the β-anomer of the sugar from the α-anomer, via the process of mutarotation. Although mutarotation from one anomer to another with some sugars is very rapid, the inter-conversion of α-galactose and β-galactose is relatively slow. The ratio of agalactose to β-galactose where mutarotation is allowed to take place until an equilibrium is achieved, is approximately 3:7. Thus, during a D-galactose determination reaction, there is a very rapid oxidation of the β-galactose in the sample by β-galactose dehydrogenase, followed by a very slow, “mutarotation dependent”, conversion of the remaining approximately 30 % of D-galactose that is in the α-anomeric form; using the level of β-galactose dehydrogenase employed in traditional kits, as soon as chemical mutarotation takes place, the majority of the β-galactose product is immediately converted to D-galactonic acid and NADH. Thus, above a certain point, regardless of how much more β-galactose dehydrogenase is employed in the assay, the total reaction time will always effectively remain the same, as the limiting factor is the non-enzymatic conversion of the α-anomer into that of the β-anomer (see figure 1). This prevents the commonly used strategy, of adding more of a readily available/inexpensive enzyme to a reaction in order to increase the speed of an enzymatic determination, being employed. This fundamental “limitation” in the quantitative determination of free D-galactose and/or L-arabinose, or these monosaccharides as released (or synthesized) from other molecules, such as lactose, D-galacose-1-phosphate, galactosyl-sucrose oligosaccharides (such as raffinose), galactan, galactomannan, arabinan and arabinogalactan, has not previously been described anywhere in the literature, most likely because of the high cost IE 04 08 48 of β-galactose dehydrogenase. However, the availability of inexpensive recombinant βgalactose dehydrogenase (i.e. Megazyme product E-GALDH), now makes it possible to incorporate much more of this enzyme into the assay, and thus the ability to overcome the fundamental mutarotation hurdle is currently of very great value.

Example 2 Assay Kit based on galactose mutarotase.

This invention describes a simple technique that can be universally applied to efficiently overcome the fundamental mutarotation hurdle presented when measuring free Dgalactose and/or L-arabinose, or these monosaccharides as released (or synthesized) from other molecules, such as lactose, D-galacose-1-phosphate, galactosyl-sucrose oligosaccharides (such as raffinose), galactan, galactomannan, arabinan and arabinogalactan, with all existing enzymatic assay kit products based on β-galactose dehy±ogenase and NAD+. As the cause of the very slow approach to the endpoint of all existing enzymatic test kits for free D-galactose and/or L-arabinose, is the conversion of α-D-galactose into β-D-galactose (or the same interconversions of L-arabinose anomers) by non-enzymatic mutarotation, by incorporating galactose mutarotase (an enzyme that specifically catalyses the same inter-conversions; synonyms: mutarotase. aldose mutarotase, galactose-1-epimerase, aldose-1-epimerase) into the assay system (see equation 4), the time taken to reach the endpoint of the reaction can be dramatically and efficiently reduced (see figures 1 and 2). (galactose mutarotase) (4) a-D-Galactose ◄-► β-D-galactose For instance, when galactose mutarotase GalM from E. coli is incorporated into the assay system as defined by equations 5 and 6, the addition of increasing amounts of β-galactose dehydrogenase does now result in a respective decrease in the amount of time required to reach the end point of the reaction (see figure 2). However, it is important to note that any galactose mutarotase could be employed in this application, for instance the galactose mutarotase termed “mutarotase” supplied by Biozyme Laboratories Limited, works IE 0 4 0 8 4 8 equally as well (see figure 4). This enzyme is offered by many suppliers, is purified from porcine kidney, and although is commonly referred to as “mutarotase”, is more formally a galactose mutarotase.

Experimental Demonstration The following experiment was performed to demonstrate the effect of addition of GalM from E. coli to the assay system, comprising equations 5 and 6 below, for the quantification of free D-galactose: (galactose mutarotase) (5) a-D-Galactose ◄-► β-D-galactose (β-galactose dehydrogenase) (6) β-D-Galactose + NAD+ -► D-galactonic acid + NADH The reaction mixtures comprised: 0.2 mL of 2 M Tris/HCl buffer, pH 8.6 containing 40 mM EDTA 0.1 mL of 8 mg/mL NAD+ 0.2 mL of 0.5 (assays 1-7) or 0.4 (assays 8-10) mg/mL D-galactose 0.00 - 0.02 mL of GalM from E. coli 0.02 - 0.08 mL of β-galactose dehydrogenase at 100 U/mL 2.12 - 2.20 mL of deionised H2O The reactions were performed at 25.8°C, and a summary of the results is presented in Table 1.

IE 0 4 0 8 4 8 Results and Conclusions Assay mL of GalM mL of β-galactose dehydrogenase Endpoint of the reaction (minutes) 1 0.02 0.08 ~3 2 0.02 0.06 ~4 3 0.02 0.04 ~6 4 0.02 0.02 ~9 5 0.01 0.02 ~9 6 0.00 0.02 - 7 0.00 0.02 >20 8 0.00 0.02 ~36 9 0.00 0.04 ~28 10 0.00 0.08 ~24 Tablel. The effect on the time taken to reach the endpoint of the reaction when varying the levels of galactose mutarotase (GalM) and β-galactose dehydrogenase.

From this simple experiment, it can be seen that when the amount of β-galactose dehydrogenase in the assay is kept the same at 0.02 mL, and the level of GalM is increased from 0.00 mL to 0.01 or 0.02 mL (assays 7, 5 and 4, respectively), the endpoint is reached in less than half the time, i.e. approximately 9 minutes as opposed to > 20 minutes. It can also be see that if the amount of β-galactose dehydrogenase in the assay is increased progressively from 0.02 to 0.08 mL (assays 4, 3, 2 and 1, respectively), while keeping the level of GalM the same at 0.02 mL, the endpoint is reached progressively faster (improving from approximately 9 minutes to approximately 3 minutes). When using 0.02 mL of GalM and 0.08 mL of β-galactose dehydrogenase, the endpoint is reached in approximately 3 min at 25.8°C. Other commercial products for the measurement of D-galactose, that do not incorporate GalM, would take approximately 30 minutes to perform the same reaction (see figure 3).

IE 04 0 8 4 8 It should be noted that the levels of both GalM and β-galactose dehydrogenase required to achieve the 3 minute endpoint reaction above are commercially viable quantities of these reagents, and in both cases would not lead to any deleterious effects on the performance of the assay.

Specificity of Galactose Mutarotase Galactose mutarotase is active on D-galactose, L-arabinose, D-xylose, maltose, lactose, D-fucose, D-fructose and D-glucose. However, an assay system incorporating galactose mutarotase has only been described for the determination of glucose with glucose oxidase; for instance, there are accounts of the use of “mutarotase” from pig (porcine) kidney to convert α-D-glucose into β-D-glucose to act as a substrate for glucose oxidase, that only recognizes the β-anomer (for examples see equations 7, 8 and 9). However, there are no accounts of the requirement to convert α-D-galactose into β-D-galactose, or α-L-arabinose into β-L-arabinose, or the means of doing so, or the potential applications thereof. (mutarotase) (7) a-D-Glucose ◄-► β-D-glucose (glucose oxidase) (8) β-D-Glucose + O2 -► D-glucono-6-lactone + H2O2 (peroxidase) (9) H2O2 + p-hydroxybenzoic acid + 4-aminoantipyrine -> quinoneimine + H2O Due to the broad specificity of galactose mutarotase, it may be possible to use this assay protocol for other sugars in addition to D-galactose and L-arabinose, such as D-xylose, maltose, lactose, D-fucose, and D-fructose, using appropriate dehydrogenases.

There are many suppliers of the enzyme termed “mutarotase” from porcine kidney, e.g. Roche, Biozyme, Calzyme, and Calbiochem. There are, however, no commercial IE 04 0 8 48 suppliers of the enzyme termed “galactose mutarotase” (GalM) from E. coli, though this enzyme has been biochemically characterized in the literature and the corresponding gene identified as galM. This gene has been cloned by Megazyme and active recombinant protein produced that possesses the necessary biochemical characteristics for this invention (see “Experimental Demonstration” section above).

Potential Applications of the Invention The primary applications of this invention include (1) the rapid measurement of free Dgalactose, and D-galactose as released by β-galactosidase from lactose, in milk, dairy products and many other materials, and (2) the rapid measurement of free D-galactose and D-galactose as released by phosphatase from D-galactose-1-phosphate, in the blood of newborn babies, as a diagnostic test for Galactos(a)emia. As can be seen from figure 3, the addition of galactose mutarotase to competitor products that contain β-galactose dehydrogenase, as would be expected, speeds up the determination of D-galactose.

There are however many other applications involving the measurement of principally, though not exclusively, free D-galactose and/or L-arabinose, or these monosaccharides as released (or synthesized) from other molecules, such as lactose, D-galacose-1-phosphate, galactosyl-sucrose oligosaccharides (such as raffinose), galactan, galactomannan, arabinan and arabinogalactan. Applications include the rapid assay of the following analytes: (a) Lactose (e.g. in milk, cheese, dairy products, foods for the lactose intolerant, etc; see following reaction scheme): (β-galactosidase) (10) Lactose + H2O -► D-galactose + D-glucose (galactose mutarotase) (11) a-D-Galactose ·<-► β-D-galactose IE 040848 (β-galactose dehydrogenase) (12) β-D-Galactose + NAD+-► D-galactonic acid + NADH + H+ (b) D-Galactose (e.g. in blood, milk, etc; see following reaction scheme): (galactose mutarotase) (13) a-D-Galactose ◄-► β-D-galactose (β-galactose dehydrogenase) (14) β-D-Galactose + NAD+-► D-galactonic acid + NADH + H+ (c) D-Galactose-1-phosphate (e.g. in blood; see following reaction scheme): (phosphatase) (15) D-Galactose-1-phosphate + H2O -► D-galactose + P, (galactose mutarotase) (16) a-D-Galactose ◄-► β-D-galactose (β-galactose dehydrogenase) (17) β-D-Galactose + NAD+-► D-galactonic acid + NADH + H+ (d) L-Arabinose (e.g. as a sweetener in foods and beverages, and in pharmaceuticals, vegetables, fruit, wine, etc; see following reaction scheme): (galactose mutarotase) (18) α-L-Arabinose <-► β-L-arabinose (β-galactose dehydrogenase) IE 04 084 8 (19) β-L-Arabinose + NAD+-► L-arabinonic acid + NADH + H+ (e) D-Galactose after release from galactan (see following reaction scheme): (galactanase, galactosidase and/or other enzyme(s) if required) (or chemical hydrolysis) (20) Galactan + H2O -► D-galactose (galactose mutarotase) (21) a-D-Galactose ◄-► β-D-galactose (β-galactose dehydrogenase) (22) β-D-Galactose + NAD+-► D-galactonic acid + NADH + H+ (f) D-Galactose after release from galactomannan (see following reaction scheme): (mannanase, galactosidase, mannosidase and/or other enzyme(s) if required) (or chemical hydrolysis) (23) Galactomannan + H2O -► D-galactose + D-mannose (galactose mutarotase) (24) a-D-Galactose ◄-► β-D-galactose (β-galactose dehydrogenase) (25) β-D-Galactose + NAD+-► D-galactonic acid + NADH + H+ (g) D-Galactose after release from galactooligosaccharides (see following reaction scheme): (galactosidase and/or other enzyme(s) if required) (or chemical hydrolysis) (26) Galactooligosaccharides + H2O -► D-galactose IE Ο 4 Ο 8 4 8 (galactose mutarotase) (27) α-D-Galactose ◄-► β-D-galactose (β-galactose dehydrogenase) (28) β-D-Galactose + NAD+-► D-galactonic acid + NADH + H+ (h) D-Galactose after release from complex molecules, e.g. glycoproteins (see following reaction scheme): (galactosidase, and/or other enzyme(s) if required) (or chemical hydrolysis) (29) Gal„-glycoprotein + H2O -► „D-galactose + glycoprotein (galactose mutarotase) (30) a-D-Galactose ◄-► β-D-galactose (β-galactose dehydrogenase) (31) β-D-Galactose + NAD+-► D-galactonic acid + NADH + H+ (i) D-Galactose after release from lactulose (see following reaction scheme): (galactosidase, and/or other enzyme(s) if required) (or chemical hydrolysis) (32) Lactulose + H2O -► D-galactose + D-fructose (galactose mutarotase) (33) a-D-Galactose ◄-► β-D-galactose (β-galactose dehydrogenase) (34) β-D-Galactose + NAD+-► D-galactonic acid + NADH + H+ (j) D-Galactose and L-arabinose after release from arabinogalactan (see following reaction scheme): IE 04 08 48 (arabinanase, arabinofuranosidase, galactanase, galactosidase and/or other enzyme(s) if required) (or chemical hydrolysis) (35) Arabinogalactan + H2O -► D-galactose + L-arabinose (galactose mutarotase) (36) α-L-Arabinose <-► β-L-arabinose (37) a-D-Galactose ◄-► β-D-galactose (β-galactose dehydrogenase) (38) β-D-Galactose + NAD+-► D-galactonic acid + NADH + H+ (39) β-L-Arabinose + NAD+-► D-arabinonic acid + NADH + H+ (k) D-Galactose after release from galactobiose (see following reaction scheme): (galactosidase, and/or other enzyme(s) if required) (or chemical hydrolysis) (40) Galactobiose + H2O -► 2 D-galactose (galactose mutarotase) (41) a-D-Galactose ◄-► β-D-galactose (β-galactose dehydrogenase) (42) β-D-Galactose + NAD+-► D-galactonic acid + NADH + H+ (l) L-Arabinose after release from arabinoxylan (see following reaction scheme): (xylanase; arabinofuranosidase; glucuronidase, esterase and/or other enzyme(s) if required) (or chemical hydrolysis) (43) Arabinoxylan + H2O -► L-arabinose + other monosaccharides IE Ο 4 Ο 8 4 8 (galactose mutarotase) (44) a-L-Arabinose ◄-► β-L-arabinose 5 (45) (β-galactose dehydrogenase) β-L-Arabinose + NAD+-► L-arabinonic acid + NADH + H+ (m) L-Arabinose after release from arabinan (e.g. in fruit juice manufacture; see following reaction scheme): (eWo-arabinanase; ew-arabinanase and/or other enzyme(s) if required) (or chemical hydrolysis) (46) Arabinan + H2O -► L-arabinose 15 (47) (galactose mutarotase) a-L-Arabinose ◄-► β-L-arabinose (48) (β-galactose dehydrogenase) β-L-Arabinose + NAD+-► L-arabinonic acid + NADH + H+ 20 (n) L-Arabinose after release from complex molecules, e.g. glycoproteins (see following reaction scheme): (arabinofuranosidase and/or other enzyme(s) if required) (or chemical hydrolysis) (49) Ara„-glycoprotein + H2O -► «L-arabinose + glycoprotein (galactose mutarotase) (50) a-L-Arabinose ◄-► β-L-arabinose 30 (51) (β-galactose dehydrogenase) β-L-Arabinose + NAD -► L-arabinonic acid + NADH + H IE 04 08 48 (o) L-Arabinose after release from arabinooligosaccharides (see following reaction scheme): (arabinofuranosidase and/or other enzyme(s) if required) (or chemical hydrolysis) (52) Arabinooligosaccharides + H2O -► L-arabinose (galactose mutarotase) (53) a-L-Arabinose ◄-► β-L-arabinose (β-galactose dehydrogenase) (54) β-L-Arabinose + NAD+-► L-arabinonic acid + NADH + H+ (p) L-Arabinose after release from arabinobiose (see following reaction scheme): (arabinofuranosidase and/or other enzyme(s) if required) (or chemical hydrolysis) (55) Arabinobiose + H2O -► 2 L-arabinose (galactose mutarotase) (56) a-L-Arabinose ◄-► β-L-arabinose (β-galactose dehydrogenase) (57) β-L-Arabinose + NAD+-► L-arabinonic acid + NADH + H+ The words “comprises/comprising” and the words “having/including” when used herein with reference to the present invention are used to specify the presence of stated features, integers, steps or components but does not preclude the presence or addition of one or more other features, integers, steps, components or groups thereof.

IE 04 0848 It is appreciated that certain features of the invention, which are, for clarity, described in the context of separate embodiments, may also be provided in combination in a single embodiment. Conversely, various features of the invention which are, for brevity, described in the context of a single embodiment, may also be provided separately or in any suitable sub-combination.

Claims (5)

Claims

1. An assay kit for the measurement of free D-galactose and/or L-arabinose in a sample, the kit comprising galactose mutarotase and β-galactose dehydrogenase.

2. An assay kit as claimed in claim 1 further comprising NAD + .

3. An assay kit as claimed in claim 1 or 2 wherein the galactose mutarotase is selected from GalM derived from E. coli, porcine kidney mutarose, or any other mutarotase catalyzing the interconversion of a- and β-D-galactose and/or a- and β-Larabinose. 4. An assay kit as claimed in any preceding claim further comprising a reagent capable of hydrolysing molecules containing D-galactose and/or L-arabinose, to yield the free mono- or di-saccharide.

4. The assay kit as claimed in any preceding claim comprising at least one enzyme capable of releasing free D-galactose and/or L-arabinose from larger molecules, or capable of assisting other enzymes in so releasing D-galactose and/or L-arabinose, the enzyme being selected from the group consisting of β-galactosidase, β-galactanase, agalactosidase,, endo-arabinanase, ew-arabinanase, α-L-arabinofuranosidase, acid phosphatase, alkaline phosphatase, β-mannanase, β-mannosidase, β-xylanase, aglucuronidase, esterase, and xylan acetyl-esterase.

5. An assay kit substantially as described herein with reference to the Examples and/or the accompanying drawings.