Heterologous expression of VHb can improve the yield and quality of biocontrol fungus Paecilomyces lilacinus, during submerged fermentation

Journal of Biotechnology

Volumn 187, Issue , 2014, Pages 147-153

  Zhang, Shumeng ^a   Wang, Jieping ^a,b   Wei, Yale ^a   Tang, Qing ^a   Ali, Maria Kanwal ^a   He, Jin ^a  

^a HUAZHONG AGRICULTURAL UNIVERSITY   (China)

^b INSTITUTE OF PLANT PROTECTION   (China)

Author keywords

Agrobacterium tumefaciens mediated transformation (ATMT); Fermentation, biomass; Paecilomyces lilacinus; Spore production; Vitreoscilla hemoglobin (VHb)

Indexed keywords

BIOCONTROL; GENES; QUALITY CONTROL;

AGROBACTERIUM TUMEFACIENS-MEDIATED TRANSFORMATION; ANAEROBIC CONDITIONS; HETEROLOGOUS EXPRESSION; INDUSTRIAL FERMENTATION; PAECILOMYCES LILACINUS; PLANT-PARASITIC NEMATODES; SUBMERGED FERMENTATION; VITREOSCILLA HEMOGLOBIN;

FERMENTATION;

CHITINASE; DISSOLVED OXYGEN; PROTEINASE; HEMOGLOBIN; OXYGEN; UNCLASSIFIED DRUG; VITREOSCILLA HEMOGLOBIN; BACTERIAL PROTEIN; BIOLOGICAL CONTROL AGENT; HEMOGLOBIN PROTEIN, VITREOSCILLA; HYBRID PROTEIN; PEPTIDE HYDROLASE; TRUNCATED HEMOGLOBIN;

AGROBACTERIUM TUMEFACIENS; ARTICLE; BATCH FERMENTATION; BIOLOGICAL PEST CONTROL; BIOMASS; ENZYME RELEASE; FUNGAL GENE; FUNGAL STRAIN; FUNGUS; FUNGUS SPORE; GENE EXPRESSION; HETEROLOGOUS EXPRESSION; MARKER GENE; NEMATODE; NONHUMAN; NUCLEOTIDE SEQUENCE; PLANT DISEASE; PRIORITY JOURNAL; PROMOTER REGION; PURPUREOCILLIUM LILACINUM; SOIL ANALYSIS; SUBMERGED FERMENTATION; VHB GENE; BIOREACTOR; CONTROLLED STUDY; ENERGY CONSUMPTION; GENOME; LARGE SCALE PRODUCTION; BIOENGINEERING; BIOLOGICAL CONTROL AGENT; CHEMISTRY; FERMENTATION; GENETICS; ISOLATION AND PURIFICATION; METABOLISM; PAECILOMYCES; PHYSIOLOGY;

BACTERIAL PROTEINS; BIOENGINEERING; BIOLOGICAL CONTROL AGENTS; BIOMASS; CHITINASE; FERMENTATION; PAECILOMYCES; PEPTIDE HYDROLASES; RECOMBINANT FUSION PROTEINS; SPORES, FUNGAL; TRUNCATED HEMOGLOBINS;

EID: 84906510612     PISSN: 01681656     EISSN: 18734863     Source Type: Journal    
DOI: 10.1016/j.jbiotec.2014.07.438     Document Type: Article

References (38)

1. Anastasiadis, I.A., Giannakou, I.O., Prophetou-Athanasiadou, D.A., Gowen, S.R., 2008. The combined effect of the application of a biocontrol agent Paecilomyces lilacinus, with various practices for the control of root-knot nematodes. Crop Prot. 27, 352-361.
2. Atkins S.D., Clark I.M., Pande S., Hirsch P.R., Kerry B.R. The use of real-time PCR and species-specific primers for the identification and monitoring of Paecilomyces lilacinus. FEMS Microbiol. Ecol. 2005, 51:257-264.
3. Cardoza R.E., Vizcaino J.A., Hermosa M.R., Monte E., Gutierrez S.A. A comparison of the phenotypic and genetic stability of recombinant Trichoderma spp. generated by protoplast- and Agrobacterium-mediated transformation. J. Microbiol. 2006, 44:383-395.
4. de Groot M.J., Bundock P., Hooykaas P.J., Beijersbergen A.G. Agrobacterium tumefaciens mediated transformation of filamentous fungi. Nat. Biotechnol. 1998, 16:839-842.
5. Flowers J.L., Vaillancourt L.J. Parameters affecting the efficiency of Agrobacterium tumefaciens-mediated transformation of Colletotrichum graminicola. Curr. Genet. 2005, 48:380-388.
6. Frey, A.D., Shepherd, M., Jokipii-Lukkari, S., Häggman, H., Kallio, P.T., 2011. The single-domain globin of Vitreoscilla, augmentation of aerobic metabolism for biotechnological applications. Adv. Microb. Physiol. 58, 81-139.
7. Geckil H., Stark B.C., Webster D.A. Cell growth and oxygen uptake of Escherichia coli and Pseudomonas aeruginosa are differently effected by the genetically engineered Vitreoscilla hemoglobin gene. J. Biotechnol. 2001, 85:57-66.
8. Gintis, B.O., Morgan-Jones, G., Rodriguez-Kibana, R., 1983. Fungi associated with several developmental stages of Heterodera glycines from an Alabama soybean field soil. Nematropica 13, 181-200.
9. Hashem M., Abo-Elyousr K.A. Management of the root-knot nematode Meloidogyne incognita on tomato with combinations of different biocontrol organisms. Crop Prot. 2011, 30:285-292.
10. Inoue I., Namiki F., Tsuge T. Plant colonization by the vascular wilt fungus Fusarium oxysporum requires FOW1, a gene encoding a mitochondrial protein. Plant Cell 2002, 14:1869-1883.
11. Isarankura-Na-Ayudhya C., Tansila N., Worachartcheewan A., Bülow L., Prachayasittikul V. Biochemical and cellular investigation of Vitreoscilla hemoglobin (VHb) variants possessing efficient peroxidase activity. J. Microbiol. Biotechnol. 2010, 20:532-541.
12. Jatala P. Biological control of plant parasitic nematodes. Annu. Rev. Phytopathol. 1986, 24:453-489.
13. Kemppainen M., Circosta A., Tagu D., Martin F., Pardo A.G. Agrobacterium-mediated transformation of the ectomycorrhizal symbiont Laccaria bicolor S238 N. Mycorrhiza 2005, 16:19-22.
14. Khan A., Williams K., Nevalainen H. Effects of Paecilomyces lilacinus protease and chitinase on the egg shell structures and hatching of Meloidogyne javanica juveniles. Biol. Control 2004, 31:346-352.
15. Khosla, C., Curtis, J.E., DeModena, J., Rinas, U., Bailey, J.E., 1990. Expression of intracellular hemoglobin improves protein synthesis in oxygen-limited Escherichia coli. Biotechnology (N.Y.) 8, 849-853.
16. Kiewnick S., Sikora R.A. Biological control of the root-knot nematode Meloidogyne incognita by Paecilomyces lilacinus strain 251. Biol. Control 2006, 38:179-187.
17. Kvist M., Ryabova E.S., Nordlander E., Bülow L. An investigation of the peroxidase activity of Vitreoscilla hemoglobin. J. Biol. Inorg. Chem. 2007, 12:324-334.
18. Li J., Li H., Bi X., Zhang K.Q. Multiple gene genealogical analyses of a nematophagous fungus Paecilomyces lilacinus from China. J. Microbiol. 2013, 51:423-429.
19. Liao, B., Wang, Y., Su, J., Liu, F., He, J., 2014. Expression of Vitreoscilla hemoglobin in Bacillus thuringiensis BMB171 can promote manganese(II) oxidation under oxygen-restricted condition. Ann. Microbiol. doi:10.1007/s13213-014-0825-z.
20. Michielse C.B., Arentshorst M., Ram A.F., Van den Hondel C.A. Agrobacterium-mediated transformation leads to improved gene replacement efficiency in Aspergillus awamori. Fungal Genet. Biol. 2005, 42:9-19.
21. Michielse, C.B., Hooykaas, P.J., Van den Hondel, C.A., Ram, A.F., 2008. Agrobacterium-mediated transformation of the filamentous fungus Aspergillus awamori. Nat. Protoc. 3, 1671-1678.
22. Miller G.L. Use of dinitrosalicylic acid reagent for determination of reducing sugar. Anal. Chem. 1959, 31:426-428.
23. Monreal J., Reese E.T. The chitinase of Serratia marcescens. Can. J. Microbiol. 1969, 15:689-696.
24. Nicol, J.M., Turner, S.J., Coyne, D.L., den Nijs, L., Hockland S., Tahna Maafi, Z., 2011. Current nematode threats to world agriculture. In: Jones, J., Gheysen, G., Fenoll, C. (Eds.), Genomics and molecular genetics of plant-nematode interactions. Springer, Dordrecht, pp. 21-43.
25. Pitt D., Poole P.C. Calcium induced conidiation in penicillium notatum in submerge culture. Trans. Br. Mycol. Soc. 1981, 76:219-230.
26. Reader U., Broda P. Rapid preparation of DNA from filamentous fungi. Lett. Appl. Microbiol. 1985, 1:17-20.
27. Roberts W.K., Selitrennikoff C.P. Plant and bacterial chitinases differ in antifungal activity. J. Gen. Microbiol. 1988, 134:169-176.
28. Rolland, S., Jobic, C., Fèvre, M., Bruel, C., 2003. Agrobacterium-mediated transformation of Botrytis cinerea, simple purification of monokaryotic transformants and rapid conidia-based identification of the transfer-DNA host genomic DNA flanking sequences. Curr. Genet. 44, 164-171.
29. Siddiqui, Z.A., Futai, K., 2009. Biocontrol of Meloidogyne incognita on tomato using antagonistic fungi, plant-growth-promoting rhizobacteria and cattle manure. Pest. Manag. Sci. 65, 943-948.
30. Sugui, J.A., Chang, Y.C., Kwon-Chung, K.J., 2005. Agrobacterium tumefaciens-mediated transformation of Aspergillus fumigatus: an efficient tool for insertional mutagenesis and targeted gene disruption. Appl. Environ. Microbiol. 71, 1798-1802.
31. Wakabayashi S., Matusbra H., Webster D.A. Primary sequence of a dimeric bacterial haemoglobin from Vitreoscilla. Nature 1986, 322:481-483.
32. Wang J.P., Wang J.X., Liu F., Pan C.S. Enhancing the virulence of Paecilomyces lilacinus against Meloidogyne incognita eggs by overexpression of a serine protease. Biotechnol. Lett. 2010, 32:1159-1166.
33. Wittenberg J.B. The molecular mechanism of hemoglobin-faeilitated oxygen diffusion. J. Biol. Chem. 1966, 241:104-114.
34. Wu, Y., Yang, S.L., 1997. Regulation and function of Vitreoscilla hemoglobin gene. Sheng Wu Gong Cheng Xue Bao 13, l-5.
35. Xu J., Wang L., Ridgway D., Gu T., Moo-Young M. Increased heterologous protein production in Aspergillus niger fermentation through extracellular proteases inhibition by pelleted growth. Biotechnol. Prog. 2000, 16:222-227.
36. Yamada T., Makimura K., Hisajima T., Ito M., Umeda Y., Abe S. Genetic transformation of the dermatophyte, Trichophyton mentagrophytes, based on the use of G418 resistance as a dominant selectable marker. J. Dermatol. Sci. 2008, 49:53-61.
37. Yang J., Zhao X., Liang L., Xia Z., Lei L., Niu X., Zou C., Zhang K.Q. Overexpression of a cuticle-degrading protease Ver112 increases the nematicidal activity of Paecilomyces lilacinus. Appl. Microbiol. Biotechnol. 2011, 89:1895-1903.
38. Zhang L., Li Y., Wang Z., Xia Y., Chen W., Tang K. Recent developments and future prospects of Vitreoscilla hemoglobin application in metabolic engineering. Biotechnol. Adv. 2007, 25:123-136.