Production of extracellular protease enzyme by aspergillus niger / (Record no. 3569)

MARC details
000 -LEADER
fixed length control field 03530nam a2200265 a 4500
001 - CONTROL NUMBER
control field vtls000066698
003 - CONTROL NUMBER IDENTIFIER
control field KUKTEM
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20251114204527.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 121121t2012 my a f m 000 0 eng d
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number THE0004127(Local)
039 #9 - LEVEL OF BIBLIOGRAPHIC CONTROL AND CODING DETAIL [OBSOLETE]
Level of rules in bibliographic description 201905132111
Level of effort used to assign nonsubject heading access points farhana
-- 201211211036
-- Fida
040 ## - CATALOGING SOURCE
Original cataloging agency UMP
090 ## - LOCALLY ASSIGNED LC-TYPE CALL NUMBER (OCLC); LOCAL CALL NUMBER (RLIN)
Classification number (OCLC) (R) ; Classification number, CALL (RLIN) (NR) TP156.F4 K43 2012 rs Bc.
100 0# - MAIN ENTRY--PERSONAL NAME
Personal name Siti Khairunnisa Daud
245 10 - TITLE STATEMENT
Title Production of extracellular protease enzyme by aspergillus niger /
Statement of responsibility, etc. Siti Khairunnisa Daud
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. Kuantan, Pahang :
Name of publisher, distributor, etc. UMP,
Date of publication, distribution, etc. 2012
300 ## - PHYSICAL DESCRIPTION
Extent xiv, 67 p. :
Other physical details ill. ;
Dimensions 30 cm. +
Accompanying material 1 CD-ROM
502 ## - DISSERTATION NOTE
Dissertation note Project paper (Bachelor of Chemical Engineering in Biotechnology) -- Universiti Malaysia Pahang - 2012
504 ## - BIBLIOGRAPHY, ETC. NOTE
Bibliography, etc. note Bibliography: p. 54-61
520 ## - SUMMARY, ETC.
Summary, etc. The research aimed to study the production of extracellular protease enzyme using potato peel extract as the additional carbon source for Aspergillus niger. Proteases are catalytically functioned to hydrolyze or breakdown the peptide bonds of proteins. Proteases are found to be used in many biotechnological processes and industrial applications such as in baking industry for gluten development, dairy industry as milk-clotting agents and pharmaceutical industries. Wastes from the agricultural and food industry gives out serious problem and as an action of initiative, those wastes can be used up and converted into value added materials as well as cost-effective substrates for fermentation of extracellular protease enzyme. Furthermore, in order to produce high yields of protease enzymes, the optimization of parameters is considered vital since it takes a long time and expensive to be optimized conventionally. This study was performed by using Response Surface Methodology (Central Composite Design). Aspergillus niger had been chosen as biomass while potato peel from the agricultural and food industry was used as additional substrate in this study. The potato peel will be grinded and blended with peel:water ratio of 1:3. The fermentation study will be take place in the shake flasks and several parameters were optimized for higher protease enzyme activity. Three factors were taken into considerations which were the pH of the fermentation medium (pH 3.5 – pH 7.5), the substrate concentration (20 g/l – 60 g/l) and the agitation speed (100 rpm – 300 rpm). From OFAT analysis, protease enzyme showed the optimum activity at pH 5.50, 40 g/l and 200 rpm with 1.23 U/ml, 1.57 U/ml and 1.38 U/ml, respectively while RSM results depicted that the optimum values of each parameter were 5.5 for pH, 40 g/l of substrates concentration and 200 rpm of agitation speed which gave out the optimum protease activity of 2.4563 U/ml. As the conclusion, RSM is the best tool used to identify the correlation between controlled independent factors and observed dependent responses and the utilization of waste as the fermentation substrates is highly acceptable due to its higher protease activity. For future study, it is recommended for an optimization of potato peel extracts concentration as the main carbon source, the application of genetic engineering in the enzyme production, further scale up protease production using a bioreactor and purification and toxicology studies on protease enzyme for further used by human, food and pharmaceutical industries.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Fermentation
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Proteolytic enzymes
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Aspergillus niger
Holdings
Withdrawn status Lost status Damaged status Not for loan Home library Current library Date acquired Total checkouts Full call number Barcode Date last seen Copy number Price effective from Koha item type
  Not lost   Not for loan UMPLIB GAMBANG UMPLIB GAMBANG 04/09/2019   TP156.F4 K43 2012 rs Bc. 0000068234 04/09/2019 1 04/09/2019 Final Year Report
  Not lost   Not for loan UMPLIB GAMBANG UMPLIB GAMBANG 04/09/2019   CD 6409 | TP156.F4 K43 2012 rs Bc. 0000068235 04/09/2019 1 04/09/2019 Final Year Report

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