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Eastern Washington University

Developing a vector for expressing serratiopeptidase in Lactococcus lactis

Abstract

dc:description.abstract

<p>Chronic inflammation stems from the inability of the body to resolve acute inflammation. Chronic inflammation is a growing health concern, as nearly 60% of Americans reported coping with at least one chronic condition (as of 2014). On a world scale, three fifths of deaths result from a chronic inflammation disease. Treatments for chronic inflammation include lifestyle changes (diet and exercise) and a variety of conventional drugs. Beyond these treatments, supplementing the body with systemic enzymes may attenuate inflammation. One promising enzyme is serratiopeptidase. Serratiopeptidase is a serine protease expressed by Serratia marcescens which has demonstrated anti-inflammatory, anti-edemic, and analgesic activity in laboratory studies and pre-clinical trials. Clinical trial data is less convincing, likely because the enzyme delivered is not bioavailable to the body after it passes through the stomach. To circumvent this issue, we proposed developing a plasmid vector that, when transformed into the probiotic Lactococcus lactis, would allow for bioactive serratiopeptidase production within the gut; thus, increasing bioavailability. The vector designed was delivered from the synthesis company in two fragments (they failed to assemble to full vector). After successfully, assembling the vector, the selection system in the commercial L. lactis strain we chose did not work as advertised in our hands. We introduced antibiotic resistance into the vector to facilitate the selection process after transformation. Unfortunately, the vector with antibiotic failed to transform L. lactis indicating some unknown problem with the vector / host system.</p>

Degree

thesis:*
Name thesis:degree_name
Master of Science (MS) in Biology
Level thesis:degree_level
Thesis
Discipline thesis:degree_discipline
Biology
Year
2021

Author and committee

dc:creator, dc:contributor.*
Author dc:creator
  • Mauzy, Taylor C

Subjects

dc:subject × 2

Rights

dc:rights
Statement dc:rights
  • Access is available to all users

Identifiers

dc:identifier.*
Repository record dc:identifier
https://dc.ewu.edu/theses/724
OAI identifier oai:identifier
oai:dc.ewu.edu:theses-1722

Chain of custody

source
Harvested from
Eastern Washington University
Base URL
dc.ewu.edu/do/oai/
Last updated
2026-07-24
Source record
OAI-PMH GetRecord
citation

Mauzy, Taylor C. Developing a vector for expressing serratiopeptidase in Lactococcus lactis. Thesis thesis, 2021. https://dc.ewu.edu/theses/724