Biotransformation of soluble starch to cyclodextrin using immobilized recombinant escherichia coli on hollow fiber membrane / (Record no. 99926)

MARC details
000 -LEADER
fixed length control field 04716ntm a2200373 i 4500
003 - CONTROL NUMBER IDENTIFIER
control field MY-KuUP
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20251125110804.0
006 - FIXED-LENGTH DATA ELEMENTS--ADDITIONAL MATERIAL CHARACTERISTICS
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007 - PHYSICAL DESCRIPTION FIXED FIELD--GENERAL INFORMATION
fixed length control field ta
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 230825t20232023my a|||fr|||| 000 0 eng d
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number THE0009701 (Local)
Qualifying information Hardback
040 ## - CATALOGING SOURCE
Original cataloging agency UMP
Language of cataloging eng
Transcribing agency UMP
Description conventions rda
090 ## - LOCALLY ASSIGNED LC-TYPE CALL NUMBER (OCLC); LOCAL CALL NUMBER (RLIN)
Classification number (OCLC) (R) ; Classification number, CALL (RLIN) (NR) FTKKP .N335 2023 r Thesis
100 1# - MAIN ENTRY--PERSONAL NAME
Personal name Nur Nadia Binti Mohd Zakaria,
Relator term author.
245 10 - TITLE STATEMENT
Title Biotransformation of soluble starch to cyclodextrin using immobilized recombinant escherichia coli on hollow fiber membrane /
Statement of responsibility, etc. Nur Nadia Binti Mohd Zakaria
264 #1 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Place of production, publication, distribution, manufacture Kuantan, Pahang :
Name of producer, publisher, distributor, manufacturer UMP,
Date of production, publication, distribution, manufacture, or copyright notice 2023
264 #4 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Date of production, publication, distribution, manufacture, or copyright notice ©2023
300 ## - PHYSICAL DESCRIPTION
Extent xvii, 136 pages :
Other physical details illustrations (some color) ;
Dimensions 30 cm. +
Accompanying material 1 CD-ROM
336 ## - CONTENT TYPE
Source rdacontent
Content type term text
336 ## - CONTENT TYPE
Source rdacontent
Content type term text
337 ## - MEDIA TYPE
Source rdamedia
Media type term unmediated
337 ## - MEDIA TYPE
Source rdamedia
Media type term computer
338 ## - CARRIER TYPE
Source rdacarrier
Carrier type term volume
338 ## - CARRIER TYPE
Source rdacarrier
Carrier type term computer disc
347 ## - DIGITAL FILE CHARACTERISTICS
Source rda
File type text file
Encoding format PDF
500 ## - GENERAL NOTE
General note Faculty of Chemical and Process Engineering Technology
502 ## - DISSERTATION NOTE
Dissertation note Thesis (Master of Science) -- Universiti Malaysia Pahang – 2023
504 ## - BIBLIOGRAPHY, ETC. NOTE
Bibliography, etc. note Includes bibliographical references
520 3# - SUMMARY, ETC.
Summary, etc. The growing interest of industries toward β-cyclodextrin (β-CD) is undeniably due to its unique structure that capable of forming inclusion agent. β-CD has been widely used in numerous industries such as in pharmaceutical, cosmetic and biotechnology. β-CD is form through the enzymatic reaction between cyclodextrin glucanotransferase (CGTase) and starch. The CGTase can be found naturally in Bacillus sp. However, Bacillus sp. produce low amount of CGTase. Thus, genetically modified E. coli can be used to solve the problem by producing high amount of CGTase. The drawbacks of CGTase production when using E. coli as a host is the occurrence of cell lysis. Hence, cell immobilization is an alternative way to reduce the cell lysis with high CGTase production. Adsorption is well known technique in cell immobilization. The advantage of adsorption technique is simple, direct contact between nutrients and matrix, and enhancing the cell stability with high yield of cell immobilization. Besides, kinetic study is also performed to understand the mechanism of adsorption reaction. The objectives of this study are to optimize the immobilization yield by manipulating the process parameters of the recombinant E. coli cells on the hollow fiber membrane via adsorption technique and to evaluate the performance of immobilized CGTase on the production of CD. The recombinant E. coli was immobilized on the hollow fiber membrane. The effect of contact time, temperature, agitation rate, pH and type of medium on the cell immobilization yield (cell concentration) was investigated by using one-factor-at-one-time (OFAT) method. The cell concentration by the immobilized cells showed 150 mg/ml under the conditions of 24 hr of contact time, 200 rpm and pH 7 at 30 °C by using Terrific broth. The significant of process parameters (temperature and contact time) on the immobilization yield was further optimized by using response surface methodology (RSM). Under the optimized conditions (20 hr of contact time and 35°C), ±227 mg/ml of cell concentration was recorded. The kinetic study of the adsorption of cell onto the hollow fiber membrane was also performed. Based on the correlation coefficient (R2), the best-fitted model is the Pseudo second-order kinetics model (R2 = 0.9515). Besides, the model was also fitted to Langmuir isotherm with the R2 of 0.989. The effect of reaction parameters such as substrate concentration, pH and agitation rate on production of β-CD by the immobilized cells was determined. The result showed that at 6% of substrate concentration, pH 9 and 200 rpm of agitation rate, the highest CD production of ±7.8 mg/ml was produced. Then, at the optimized reaction conditions (200 rpm, pH 8.5 and 5.5% of substrate concentration), the highest CD production (±11.6 mg/ml) was recorded. For the reaction kinetic study, it showed that the Vmax of both immobilized cells (±2.18 mg/ml.hr) and free cells (±2.25 mg/ml.hr) was almost similar. The Km value for the immobilized cells (±5.14 mg/ml) was almost the same as the free cell (±5.42 mg/ml). The immobilized cells also could retain 24.4% from its initial activity even after 6 successful cycles. Thus, these findings showed that the immobilized recombinant E. coli on the hollow fiber membrane is a promising technique to produce high concentration of β-CD.
610 20 - SUBJECT ADDED ENTRY--CORPORATE NAME
Corporate name or jurisdiction name as entry element Faculty of Chemical and Process Engineering Technology
General subdivision Dissertations
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Universities and colleges
General subdivision Dissertations
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Theses
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme Library of Congress Classification
Koha item type Thesis
Holdings
Withdrawn status Lost status Source of classification or shelving scheme Damaged status Not for loan Collection 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 Library of Congress Classification   Not for loan Reference UMPLIB GAMBANG UMPLIB GAMBANG 25/08/2023   FTKKP .N335 2023 r Thesis T000002513 25/08/2023 1 25/08/2023 Thesis
  Not lost Library of Congress Classification   Final Processing Reference UMPLIB PEKAN UMPLIB PEKAN 25/08/2023   CD13425 T000002514 25/08/2023 1 25/08/2023 Thesis

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