The GMO Handbook 2004
DOI: 10.1007/978-1-59259-801-4_4
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Genetically Modified Microorganisms

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Cited by 12 publications
(6 citation statements)
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“…Although novel disease-suppressive strains might overcome inadequate colonization of the host rhizosphere and inefficient inhibition of soil-borne pathogen growth, the discovery of taxonomically novel isolates possessing biological disease control activity becomes more difficult over time even after extensive searches. Another promising approach, exploiting genetically modified microbial strains with improved antagonistic function has been restricted or prohibited worldwide ( Migheli, 2001 ; Stemke, 2004 ). When applying BCAs in natural settings, BCAs do not act independent of their environment but interact with many indigenous microbes to become components of local microbial communities.…”
Section: Utilization Of Msbcas In Management Of Soil-borne Diseasesmentioning
confidence: 99%
“…Although novel disease-suppressive strains might overcome inadequate colonization of the host rhizosphere and inefficient inhibition of soil-borne pathogen growth, the discovery of taxonomically novel isolates possessing biological disease control activity becomes more difficult over time even after extensive searches. Another promising approach, exploiting genetically modified microbial strains with improved antagonistic function has been restricted or prohibited worldwide ( Migheli, 2001 ; Stemke, 2004 ). When applying BCAs in natural settings, BCAs do not act independent of their environment but interact with many indigenous microbes to become components of local microbial communities.…”
Section: Utilization Of Msbcas In Management Of Soil-borne Diseasesmentioning
confidence: 99%
“…There are several available protocols and methods applied for the transfer of DNA into cells, their applicability may however be general or source specific. The strategies and approaches used are often collectively termed recombinant DNA technology (Han, 2004). The term "recombinant DNA technology" comprises of an arsenal of laboratory methods used in production of a GMO and summarily includes the basic steps of; identification and isolation of the genetic trait of interest and its nucleotide sequence (gene); production of gene copies via amplification mechanisms; gene association with suitable promoter and poly A sequence and its insertion into a vector (such as plasmids); multiplication of the plasmid-bacteria construct and its subsequent recovery of construct for injection; transfer of the construct into the recipient tissue; integration and expression of gene in recipient genome; and inheritance of the gene through other generations (Beardmore and Porter, 2003).…”
Section: Gmo Engineering Processmentioning
confidence: 99%
“…The term "recombinant DNA technology" comprises of an arsenal of laboratory methods used in production of a GMO and summarily includes the basic steps of; identification and isolation of the genetic trait of interest and its nucleotide sequence (gene); production of gene copies via amplification mechanisms; gene association with suitable promoter and poly A sequence and its insertion into a vector (such as plasmids); multiplication of the plasmid-bacteria construct and its subsequent recovery of construct for injection; transfer of the construct into the recipient tissue; integration and expression of gene in recipient genome; and inheritance of the gene through other generations (Beardmore and Porter, 2003). Two principal enzymes used in recombinant DNA technology are the; restriction endonucleases (biological scissors) used to cleave DN molecules at specific points into fragments of defined sizes; and the ligases (biological glue) to join the insert and vector together (Davies and Ollier, 2001;Han, 2004;Traavik et al, 2007). The vector contains a DNA sequence, origin of replication (ori) that enables it to be replicated in the bacteria, Escherichia coli, they include biolistics, CaCl 2 -heat shock treatment or electroporation, transformation and conjugation, other processes include; gene silencing and gene splicing, lipofection, microinjection, calcium phosphate precipitation, vectors and protoplast transformation among others (Han, 2004;Olaniyan et al, 2007).…”
Section: Gmo Engineering Processmentioning
confidence: 99%
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“…Although, these innovations raise worries about the potential risks presented by the genetically altered microorganism because many of these are hazardous due to their infectious nature to humans and the environment. So, explicit conventions have been created to securely screen the utilisation of hereditarily altered dangerous organisms because these can potentially cause mass destruction of life globally, like the Cartagena Protocol on Biosafety 2 .…”
Section: Introductionmentioning
confidence: 99%