Production of Glucoamylase from Novel Strain of Alternaria Alternata under Solid State Fermentation

Author:

Nayab Durr-e-1ORCID,Akhtar Shamim1ORCID,Bangash Nazneen2ORCID,Nisa Waqar-un-3,Hayat Malik Tahir4ORCID,Zulfiqar Awais5ORCID,Niaz Mubashar6ORCID,Qayyum Abdul7ORCID,Syed Asad8ORCID,Bahkali Ali H.8,Elgorban Abdallah M.8ORCID

Affiliation:

1. Department of Botany, University of Gujrat, Pakistan

2. Department of Biosciences, COMSATS University, Islamabad, Pakistan

3. International Islamic University, H-10 Islamabad, Pakistan

4. Department of Environmental Sciences, COMSATS University, Abbottabad Campus, Islamabad, Pakistan

5. Brimbank City Council, P.O. Box 70 Sunshine, Victoria 3020, Australia

6. Atlas Environmental Laboratories, Suite 1503, Street 36 West, Manhattan, New York 10018, USA

7. Department of Agronomy, The University of Haripur, Haripur 22620, Pakistan

8. Department of Botany and Microbiology, College of Science, King Saud University, P.O. 2455, Riyadh 11451, Saudi Arabia

Abstract

Glucoamylase has an essential role as biocatalyst in various important industries of Pakistan. It is synthesized by using various fungal and bacterial strains, and different ecocultural conditions are applied under solid substrate fermentation method (SSF) to get the highest yield of glucoamylase. Alternaria alternata is an important fungus that can grow on industrial raw material like wheat bran, dried potato powder, tea leaves, rice husk, and sugar cane peel which are used as substrate. Among all, dried potato powder (10g) proved the best fermentation media for growth of fungal strain as well as maximum glucoamylase producer. Moreover, several chemical and physical states were also explored through solid substrate fermentation technique on glucoamylase yield. The highest glucoamylase production was recorded after 72 hours incubation in incubation chamber with 10g raw substrate, 1ml inoculum spore solution, 30°C temperature, and 5 pH. Further, phosphate buffer (5 pH) as moistening agent, 5% starch concentration and media additive as nitrogen (yeast extract), and carbon source (maltose) were screened for maximum glucoamylase titer ( 17.3 ± 0.05 a°U/ml/min) and the highest specific activity (39.2U/mg). These cultural conditions were most appropriate for growth of A. alternata on solid media and production of highest glucoamylase under solid state fermentation procedure that could be utilized for commercial synthesis of glucoamylase.

Funder

King Saud University

Publisher

Hindawi Limited

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine

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