國立虎尾科技大學 |

From Biofuels to Natural Products : = Microbial Metabolic Engineering for Chemical Production.

紀錄類型:	書目-語言資料,手稿 : Monograph/item
正題名/作者:	From Biofuels to Natural Products :/
其他題名:	Microbial Metabolic Engineering for Chemical Production.
作者:	Nozzi, Nicole E.
面頁冊數:	1 online resource (109 pages)
附註:	Source: Dissertation Abstracts International, Volume: 79-03(E), Section: B.
標題:	Bioengineering. -
電子資源:	click for full text (PQDT)
ISBN:	9780355462166

From Biofuels to Natural Products : = Microbial Metabolic Engineering for Chemical Production.
Nozzi, Nicole E.

From Biofuels to Natural Products :Microbial Metabolic Engineering for Chemical Production. - 1 online resource (109 pages)

Source: Dissertation Abstracts International, Volume: 79-03(E), Section: B.

Thesis (Ph.D.)--University of California, Davis, 2017.

Includes bibliographical references

This work covers three metabolic engineering projects falling into the general categories of pathway optimization, strain optimization, and pathway construction. The first project explores the functionality of isopropyl beta-D-1-thiogalactopyranoside (IPTG) inducible promoters for the control of heterologous gene expression in the freshwater cyanobacterium Synechoccocus elongatus PCC 7942 (7942). Initial experiments for the project revealed that the occurrence of unrepressed gene expression in the absence of an inducer was actually caused by the particular pathway genes of the previously established 2,3-butanediol (23BD) production pathway rather than by the choice of promoter itself. Tight control of heterologous gene expression for the production pathway was successfully achieved via the rearrangement of operon order to remove the effect of hidden constitutive promoters within pathway genes.

Electronic reproduction.
Ann Arbor, Mich. :
ProQuest,
2018

Mode of access: World Wide Web

ISBN: 9780355462166Subjects--Topical Terms:

598252
Bioengineering.
Index Terms--Genre/Form:

554714
Electronic books.

From Biofuels to Natural Products : = Microbial Metabolic Engineering for Chemical Production.
LDR:03758ntm a2200361K 4500 001 914748
005 20180724121429.5
006 m o u
007 cr mn||||a|a||
008 190606s2017 xx obm 000 0 eng d
020 $a 9780355462166
035 $a (MiAaPQ)AAI10624520
035 $a (MiAaPQ)ucdavis:17358
035 $a AAI10624520
040 $a MiAaPQ $b eng $c MiAaPQ
100 1 $a Nozzi, Nicole E. $3 1188082
245 1 0 $a From Biofuels to Natural Products : $b Microbial Metabolic Engineering for Chemical Production.
264 0 $c 2017
300 $a 1 online resource (109 pages)
336 $a text $b txt $2 rdacontent
337 $a computer $b c $2 rdamedia
338 $a online resource $b cr $2 rdacarrier
500 $a Source: Dissertation Abstracts International, Volume: 79-03(E), Section: B.
500 $a Adviser: Shota Atsumi.
502 $a Thesis (Ph.D.)--University of California, Davis, 2017.
504 $a Includes bibliographical references
520 $a This work covers three metabolic engineering projects falling into the general categories of pathway optimization, strain optimization, and pathway construction. The first project explores the functionality of isopropyl beta-D-1-thiogalactopyranoside (IPTG) inducible promoters for the control of heterologous gene expression in the freshwater cyanobacterium Synechoccocus elongatus PCC 7942 (7942). Initial experiments for the project revealed that the occurrence of unrepressed gene expression in the absence of an inducer was actually caused by the particular pathway genes of the previously established 2,3-butanediol (23BD) production pathway rather than by the choice of promoter itself. Tight control of heterologous gene expression for the production pathway was successfully achieved via the rearrangement of operon order to remove the effect of hidden constitutive promoters within pathway genes.
520 $a This same 23BD production pathway was adapted for use in the marine cyanobacterium Synechoccocus sp. PCC 7002 (7002) in the second project described here. 7002 has attracted much interest in the metabolic engineering community as a new host strain due to its rapid growth rate and increased tolerance to heat, light, and salt. After screening different systems for control of inducible gene expression, gene arrangements, and culturing conditions, production of 23BD was achieved in 7002 for the first time with a titer of 1.6 g/L after 16 days.
520 $a The final project described here outlines the design and beginnings of the construction of an engineered biosynthetic pathway for the production of the tropane alkaloid scopolamine in the model host organism Escherichia coli. Scopolamine is a muscarinic antagonist in high worldwide demand for a range of treatments, but which suffers from a limited supply from the traditional natural product sources of plant extraction and total chemical synthesis. In this new engineered pathway design the starting materials for the scopolamine ester are derived from both chemical and biological syntheses in an effort to draw from the strengths of each strategy. The bulk of the work done for this project concerned the activation of a critical pathway intermediate into a coenzyme A thioester. Given the lack of a previously characterized enzyme for this step, work was done to screen and design an enzyme capable of doing so. Despite several rounds of screening a new enzyme was not found, but the work done nevertheless has set a precedent for future endeavors in this area.
533 $a Electronic reproduction. $b Ann Arbor, Mich. : $c ProQuest, $d 2018
538 $a Mode of access: World Wide Web
650 4 $a Bioengineering. $3 598252
650 4 $a Microbiology. $3 591510
650 4 $a Biochemistry. $3 582831
655 7 $a Electronic books. $2 local $3 554714
690 $a 0202
690 $a 0410
690 $a 0487
710 2 $a ProQuest Information and Learning Co. $3 1178819
710 2 $a University of California, Davis. $b Chemistry. $3 1182773
856 4 0 $u http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=10624520 $z click for full text (PQDT)