<div>
<div>
<div>
<p>Phages, viruses that infect bacteria, have been used for many studies in understanding
fundamentals of molecular biology and taking advantage of their natural antimicrobial properties
(Harper 2021). They are often noted for their overwhelming abundance and are recognized as the
most abundant biological entities in the world (Harper 2021). The field has grown since the early
20th century, and now, there are several classes of phages that have been observed and
characterized (Ackermann 2009). Within this abundant class of biological organisms, the order
called Caudovirales, is the most populated group of phages to date (Harper 2021). In this order
of viruses, the dsDNA genome phages have 2 main components, the icosahedral capsid, and a
tail (Harper 2021). Though many tailed phages have been studied for many decades, new
information about phages is still being found. Important findings such as the CRISPR gene
editing tool adapted from phages in 2007 (Barrangou, Fremaux et al. 2007) have contributed to
new biotechnology that impacts human health. For this reason, studies on phages have proven to
be valuable in understanding fundamental biological questions and advancing basic research.
</p><p><br></p>
<p>In this dissertation, we investigated phage G, which has the largest capsid and genome of
propagated phage studied to date (Donelli 1968, Sun and Serwer 1997, Pope 2011, Hua, Huet et
al. 2017). By studying phage G, we may add to the knowledge of this relatively unexplored
group of Jumbo phages with remarkably larger genomes (>200kbp) (Yuan and Gao 2017)to
understand how their structure and function may be similar or different to the commonly studied,
smaller bacteriophages, such as T4 and λ. For a majority of these studies, we outline how our
structural biology insights of phage G using cryo-EM (cryo-Electron Microscopy) have shown
it’s icosahedral capsid of ~ 180 nm in diameter at the 5-fold icosahedral vertex is composed of
hexamer and pentamer proteins similar to what’s been discovered in other, smaller tailed phages
(González, Monroe et al. 2020). Our observations from microscopy data also show unique
mechanistic properties in phage G’s tail that are inconsistent with current model of tail
contraction within the Myoviridae family of tailed phages. Data suggest phage G’s structure and
organization of its helical tail are still similar to contractile phages such as T4 (Amos and Klug
1975, Abuladze, Gingery et al. 1994) and phi812 (Nováček, Šiborová et al. 2016), however, the mechanism of the tail sheath movement is inconsistent with the existing ideas of myophage
function (Harper 2021).</p></div></div></div>
| Identifer | oai:union.ndltd.org:purdue.edu/oai:figshare.com:article/15156780 |
| Date | 12 August 2021 |
| Creators | Brenda Gonzalez (11267193) |
| Source Sets | Purdue University |
| Detected Language | English |
| Type | Text, Thesis |
| Rights | CC BY 4.0 |
| Relation | https://figshare.com/articles/thesis/STRUCTURAL_STUDIES_OF_THE_PHAGE_G_CAPSID_AND_HELICAL_TAIL_SHEATH_USING_CRYO-EM/15156780 |
Page generated in 0.0015 seconds