[electronic resource] (Record no. 65840)

MARC details
000 -LEADER
fixed length control field nab a22 7a 4500
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 200818s2019 ua |||pss|||| 00| 0 eng d
040 ## - CATALOGING SOURCE
Original cataloging agency EAL
Transcribing agency EAL
041 ## - LANGUAGE CODE
Language code of text/sound track or separate title eng
Language code of summary or abstract ara
090 ## - LOCALLY ASSIGNED LC-TYPE CALL NUMBER (OCLC); LOCAL CALL NUMBER (RLIN)
Classification number (OCLC) (R) ; Classification number, CALL (RLIN) (NR) ART NRMJ V3 NO6 10
100 1# - MAIN ENTRY--PERSONAL NAME
Personal name Ali, Safaa M.
9 (RLIN) 31782
240 10 - UNIFORM TITLE
Uniform title Novel research in microbiology journal, 2019 v.3 (6)
Medium [electronic resource].
245 10 - TITLE STATEMENT
Title New source of cellulase production using a metagenomic technique
Medium [electronic resource]
300 ## - PHYSICAL DESCRIPTION
Extent p. 590-597.
504 ## - BIBLIOGRAPHY, ETC. NOTE
Bibliography, etc. note Includes bibliographic reference
520 ## - SUMMARY, ETC.
Summary, etc. The cellulase enzymes with high effectiveness under conditions agreeable to the industrial processes<br/>necessities are one of the keys for the successful development of chemical and drug synthesis. The soil<br/>metagenome is an affluent source for the discovery of new natural products. The objective of the current study<br/>was to identify the isolated functional gene(s) of the cellulase enzyme by using metagenomics. The plan of work<br/>composed of collection of different soil samples, isolation of total DNA, fragmentation, cloning, and expression<br/>of the isolated gene(s) in the suitable host microorganism. The total genomic DNA was extracted using a kit<br/>(QIAGEN), and then digested by different restriction enzymes BamHI. The digested fragments ranging from<br/>~300-5000 bp were ligated, cloned into pUC19 vector, and then transformed into Escherichia coli DH5?. The<br/>resulting clones were screened as cellulase producers using a qualitative method. The positive clones which<br/>showed hydrolysis on the plate were screened once more in Luria-Bertani (LB) medium. The plasmids were<br/>isolated and then tested using universal primer (M13), to detect the fragment size and sequence for the<br/>Polymerase Chain Reaction (PCR) products. This study establishes an effortless and professional method for<br/>cloning of recent cellulase genes through ecological metagenomes. In the outlook, the metagenomic guide<br/>approachs may be functional to the elevated selection of novel cellulase from the environment.<br/>
546 ## - LANGUAGE NOTE
Language note Summary in Arabic
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element cellulase production
9 (RLIN) 31783
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Soliman, Nadia A.
9 (RLIN) 31784
773 0# - HOST ITEM ENTRY
Title Novel Research in Microbiology Journal
Related parts 2019.v.3(6)
Control subfield 2537-0294
Record control number 65799
856 ## - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier http://nile.enal.sci.eg/EALE/2019/NRMJ/319/6/590.pdf
Public note Full Text Article
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Source of classification or shelving scheme alc
Articles AR
Holdings
Withdrawn status Lost status Source of classification or shelving scheme Damaged status Not for loan Home library Current library Date acquired Total Checkouts Full call number Date last seen Price effective from Koha item type
    Alphabetical Classification     Main Main 08/18/2020   ART NRMJ V3 NO6 10 08/18/2020 08/18/2020 Articles

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