An improved bioprocess for synthesis of acetohydroxamic acid using DTT (dithiothreitol) treated resting cells of Bacillus sp. APB-6

Bioresource Technology

Volumn 102, Issue 11, 2011, Pages 6579-6586

  Pandey, Deepak ^a   Singh, Rajendra ^a   Chand, Duni ^a  

^a HIMACHAL PRADESH UNIVERSITY   (India)

Author keywords

Acetohydroxamic acid; Acyltransferase; Bacillus sp. APB 6; DTT; N methylacetamide

Indexed keywords

ACETOHYDROXAMIC ACIDS; ACYLTRANSFERASE; BACILLUS SP. APB-6; DTT; N-METHYLACETAMIDE; BACILLUS SP;

AMIDES; BACILLI; SYNTHESIS (CHEMICAL); BIOTECHNOLOGY; ENVIRONMENTAL ENGINEERING;

BACTERIOLOGY;

ACETAMIDE; ACETOHYDROXAMIC ACID; ACYLTRANSFERASE; AMIDASE; DITHIOTHREITOL; HYDROCHLORIC ACID; HYDROXAMIC ACID; HYDROXYLAMINE; N METHYLACETAMIDE;

BACTERIUM; BIOCHEMISTRY; BIOTECHNOLOGY; CATALYSIS; DRUG; ENZYME ACTIVITY; REACTION KINETICS;

ARTICLE; BACILLUS; BIOPROCESS; CHEMICAL REACTION; CONTROLLED STUDY; ENZYME ACTIVITY; FREEZE DRYING; NONHUMAN; PRIORITY JOURNAL; SYNTHESIS;

ACETAMIDES; ACYLTRANSFERASES; AMIDOHYDROLASES; BACILLUS; BIOTECHNOLOGY; CULTURE MEDIA; DITHIOTHREITOL; ENZYME INDUCTION; ENZYME INHIBITORS; HYDROXAMIC ACIDS; HYDROXYLAMINE; IONS; METALS; NITRILES; RECYCLING; SUBSTRATE SPECIFICITY; TEMPERATURE; TIME FACTORS;

BACILLUS SP.;

EID: 79955464388     PISSN: 09608524     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.biortech.2011.03.071     Document Type: Article

References (28)

1. Banerjee A., Sharma R., Banerjee U.C. The nitrile degrading enzymes: current status and future prospects. Appl. Microbiol. Biotechnol. 2002, 60:33-44.
2. Brammar W.J., Clarke P.H. Induction and repression of Pseudomonas aeruginosa amidase. J. Gen. Microbiol. 1964, 37:307-319.
3. Brent B.E., Adepoju A. Effect of acetohydroxamic acid on rumen ureases. J. Anim. Sci. 1967, 26:1482.
4. Chand D., Kumar H., Sankhian U.D., Kumar D., Vitzthum F., Bhalla T.C. Treatment of simulated wastewater containing toxic amides by immobilized Rhodococcus rhodochrous NHB-2 using a highly 5-stage plag flow reactor. World J. Microbiol. Biotechnol. 2004, 20:679-686.
5. Fawcett J.K., Scott J.E. A rapid and precise method for the determination of urea. J. Clin. Pathol. 1960, 13:156-159.
6. Fishbein W.N., Carbone P.P., Hochstein H.D. Acetohydroxamate: a bacterial urease inhibitor with therapeutic potential in hyperamonemic states. Nature 1965, 208(5005):46-48.
7. Fournand D., Bigey F., Ratomahenina R., Arnaud A., Galzy P. Biocatalyst improvement for the production of short-chain hydroxamic acids. Enzyme Microbial. Technol. 1997, 20:424-431.
8. Fournad D., Arnaud A., Galzy P. Study of the acyl transfer activity of a recombinant amidase overproduced in an E. coli strain. Application for short chain hydroxamic acid and acid hydrazide synthesis. J. Mol. Catal. B. 1998, 4:77-90.
9. Fournand D., Vaysse L., Dubreucq E., Arnaud A., Galzy P. Monohydroxamic acid biosynthesis. J. Mol. Catal. B. 1998, 5:207-211.
10. Fournand D., Bigey F., Arnaud A. Acyl transfer activity of an amidase from Rhodococcus sp. R312: formation of a wide range of hydroxamic acids. Appl. Environ. Microbiol. 1998, 64:2844-2852.
11. Gao W.Y., Mitsuya H., Driscoll J.S., Johns D.G. Enhancement by hydroxyurea of the anti-human immunodeficiency virus type 1 potency of 2'-β-fluoro-2', 3'-dideoxyadenosine in peripheral blood mononuclear cells. Biochem. Pharmacol. 1995, 50:274-276.
12. Goil M.M. Effect of some - SH and other reagents on aspartate aminotransferase and l-alanine aminotransferase of Paramphistomum explanatum fischoeder, 1901. Parasitol. Res. 1978, 55(1):59-62.
13. Grossowicz N., Wainfan E., Borek E., Waelsch H. The enzymatic formation of hydroxamic acids from glutamine and asparagine. J. Biol. Chem. 1950, 187:111-125.
14. Hamer R.L., Tegeler J.J., Kurtz E.S., Allen R.C., Bailey S.C., Elliot M.E., Heller L., Hessley G.C., Przekop P., Freed B.S., White J., Martin L.I. Dibenzoxepinone hydoxylamines and hydroxamic acids: dual inhibitors of cyclooxygenase and 5-lipooxygenase with potent typical anti inflammatory activity. J. Med. Chem. 1996, 39:246-252.
15. Holmes L.B. Hydroxamic acid: a potential human teratogen that could be recommended to treat ureaplasma. Teratology 1996, 53:227-229.
16. Kasche V. Mechanism and yields in enzyme catalysed equilibrium and kinetically controlled synthesis of β-lactam antibiotics, peptides and other condensation products. Enzyme Microbial. Technol. 1986, 8:4-16.
17. Kelly M., Clarke P.H. An inducible amidase produced by a strain of Pseudomonas aeruginosa. J. Gen. Microbiol. 1962, 27:305-316.
18. Kobashi K., Hase J. Inhibition of Proteus vulgaris urease by hydroxamic acids. J. Biochem. 1967, 62(3):293-299.
19. Koide Y., Uchino M., Yamada K. Studies of collectors. IX. The floatation of a trace amount of uranium by using 2-(alkylamino) propionohydroxamic acid and cotelomer-type surfactants bearing hydroxyaminocarbonyl and pyridyl groups. Bull. Chem. Soc. Jpn. 1987, 60:3477-3483.
20. Kotlova E.K., Chestukhina C.G., Astaurova O.B., Leonova T.E., Yanenko A.S., Debaboy V.G. Isolation and primary characterization of an amidase from Rhodococcus rhodochrous. Biochemistry Mosc. 1999, 64:384-390.
21. Madhavan N.K., Roopesh K., Chacko S., Pandey A. Comparative study of amidase production by free and immobilised Escherichia coli cells. Appl. Biochem. Biotechnol. 2005, 120:97-108.
22. Maestracci M., Thiery A., Arnaud A., Galzy P. A study of the mechanism of the reactions catalyzed by the amidase from Brevibacterium sp. R312. Agric. Biol. Chem 1986, 50:2237-2241.
23. Nawaz M.S., Khan A.A., Bhattacharaya D., Siitonen P.H., Cerniglia C.E. Physical, biochemical and immunological characterization of a thermostable amidase from Klebsiella pneumoniae NCTR 1. J Bacteriol. 1996, 178:2397-2401.
24. Novo C., Farnaud S., Tata R., Clemente A., Brown P.R. Support for a three dimensional structure predicting a Cys-Glu-Lys catalytic triad for Pseudomonas aeruginosa amidase comes from site-directed mutagenesis and mutations altering substrate specificity. Biochem. J. 2002, 365:731-738.
25. Pace H.C., Brenner C. The nitrilase superfamily: classification, structure and function. Genome Biol. 2001, 2(1):0001.1-0001.9.
26. Ramakrishna C., Dave H., Ravindranathan M. Microbial metabolism of nitriles and its biotechnological potential. J. Sci. Ind. Res. 1999, 58:925-947.
27. Streeter C.L., Oltjen R.R., Slyter L.L., Fishbein W.N. Urea utilization in weathers receiving the urease inhibitor, acetohydroxamic acid. J. Anim. Sci. 1969, 29:88-93.
28. Thiėry A., Maestracci M., Arnaud A., Galzy P. Acyltransferase activity of a wide spectrum amidase of Brevibacterium sp. R312. J. Gen. Microbiol. 1986, 132:2205-2208.