Development of a galactose biosensor with galactose oxidase-immobilized epidermis of Solanum lycopersicum: Potential point-of-care testing for citrin deficiency in high-prevalence areas

Clinica Chimica Acta

Volumn 412, Issue 3-4, 2011, Pages 391-392

  Lee, Hencher H C ^a,b   Wong, Esther S C ^a   Chan, Albert Y W ^b   Choi, Martin M F ^a  

^a HONG KONG BAPTIST UNIVERSITY   (Hong Kong)

^b PRINCESS MARGARET HOSPITAL   (Hong Kong)

Author keywords

[No Author keywords available]

Indexed keywords

DISSOLVED OXYGEN; GALACTOSE; GALACTOSE OXIDASE;

AMPEROMETRIC BIOSENSOR; CITRIN DEFICIENCY; ENZYME IMMOBILIZATION; GALACTOSE BIOSENSOR; GALACTOSEMIA; HUMAN; LETTER; OXIDATION; PLANT EPIDERMIS; POINT OF CARE TESTING; PREVALENCE; PRIORITY JOURNAL; PROTEIN DEFICIENCY; REPRODUCIBILITY; SCREENING; SENSITIVITY AND SPECIFICITY; SOLANUM; SOLANUM LYCOPERSIUCM; URINALYSIS;

BIOSENSING TECHNIQUES; CALCIUM-BINDING PROTEINS; ENZYMES, IMMOBILIZED; GALACTOSE; GALACTOSE OXIDASE; HUMANS; LYCOPERSICON ESCULENTUM; ORGANIC ANION TRANSPORTERS; PLANT EPIDERMIS; POINT-OF-CARE SYSTEMS; PREVALENCE;

LYCOPERSICON ESCULENTUM;

EID: 78650230811     PISSN: 00098981     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cca.2010.10.010     Document Type: Letter

References (21)

1. Brunetti-Pierri N., Opekun A.R., Craigen W.J. Two familial cases of high blood galactose of unknown aetiology. J Inherit Metab Dis 2006, 29:762.
2. Cheung K.L., Tang N.L., Hsiao K.J., et al. Classical galactosaemia in Chinese: A case report and review of disease incidence. J Paediatr Child Health 1999, 35:399-400.
3. Ohura T., Kobayashi K., Abukawa D., et al. A novel inborn error of metabolism detected by elevated methionine and/or galactose in newborn screening: Neonatal intrahepatic cholestasis caused by citrin deficiency. Eur J Pediatr 2003, 162:317-322.
4. Tamamori A., Fujimoto A., Okano Y., et al. Effects of citrin deficiency in the perinatal period: Feasibility of newborn mass screening for citrin deficiency. Pediatr Res 2004, 56:608-614.
5. Sinasac D.S., Crackower M.A., Lee J.R., et al. Genomic structure of the adult-onset type II citrullinemia gene, SLC25A13, and cloning and expression of its mouse homologue. Genomics 1999, 62:289-292.
6. Gulce H., Ataman I., Gulce A., Yildiz A. Enzyme Microb Tech 2002, 30:41-44.
7. de Verdier C., Hjelm M. A galactose-oxidase method for the determination of galactose in blood plasma. Clin Chim Acta 1962, 7:742-744.
8. Amiss T.J., Sherman D.B., Nycz C.M., Andaluz S.A., Pitner J.B. Engineering and rapid selection of a low-affinity glucose/galactose-binding protein for a glucose biosensor. Protein Sci 2007, 16:2350-2359.
9. Dahodwala S.K., Weibel M.K., Humphrey A.E. Galactose oxidase: applications of the covalently immobilized enzyme in a packed bed configuration. Biotechnol Bioeng 1976, 18:1679-1694.
10. Taylor P.J., Kmetec E., Johnson J.M. Design, construction, and applications of a galactose selective electrode. Anal Chem 1977, 49:789-794.
11. Rajendran V., Lrudayaraj J. Detection of glucose, galactose, and lactose in milk with a microdialysis-coupled flow injection amperometric sensor. J Dairy Sci 2002, 85:1357-1361.
12. Kondakova L., Yanishpolskii V., Tertykh V., Buglova T. Galactose oxidase immobilized on silica in an analytical determination of galactose-containing carbohydrates. Anal Sci 2007, 23:97-101.
13. Han H., Li Y., Yue H., Zhou Z., Xiao D., Choi M.M. Clinical determination of glucose in human serum by a tomato skin biosensor. Clin Chim Acta 2008, 395:155-158.
14. Wen G., Zhang Y., Zhou Y., Shuang S., Dong C., Choi M.M.F. Biosensors for determination of galactose with galactose oxidase immobilized on eggshell membrane. Anal Lett 2005, 38:1519-1529.
15. Techniques in diagnostic human biochemical genetics: A laboratory manual 1991, Wiley-Liss. F.A. Hommes (Ed.).
16. Chalmers A.H., Cowley D.M., McWhinney B.C. Stability of ascorbate in urine: Relevance to analyses for ascorbate and oxalate. Clin Chem 1985, 31:1703-1705.
17. Lu Y.B., Kobayashi K., Ushikai M., et al. Frequency and distribution in East Asia of 12 mutations identified in the SLC25A13 gene of Japanese patients with citrin deficiency. J Hum Genet 2005, 50:338-346.
18. Hutchin T., Preece M.A., Hendriksz C., et al. Neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD) as a cause of liver disease in infants in the UK. J Inherit Metab 2009, 10.1007/s10545-009-1116-x.
19. Song Y.Z., Li B.X., Chen F.P., et al. Neonatal intrahepatic cholestasis caused by citrin deficiency: clinical and laboratory investigation of 13 subjects in mainland of China. Dig Liver Dis 2009, 41:683-689.
20. Nagasaka H., Okano Y., Tsukahara H., et al. Sustaining hypercitrullinemia, hypercholesterolemia and augmented oxidative stress in Japanese children with aspartate/glutamate carrier isoform 2-citrin-deficiency even during the silent period. Mol Genet Metab 2009, 97:21-26.
21. Davis J., Vaughan D.H., Cardosi M.F. Elements of biosensor construction. Enzyme Microb Tech 1995, 17:1030-1035.