scispace - formally typeset
H

Helen Rawsthorne

Researcher at North Carolina State University

Publications -  19
Citations -  1981

Helen Rawsthorne is an academic researcher from North Carolina State University. The author has contributed to research in topics: Lactococcus lactis & Fermentation. The author has an hindex of 13, co-authored 18 publications receiving 1853 citations. Previous affiliations of Helen Rawsthorne include Drexel University & University of California, Davis.

Papers
More filters
Journal ArticleDOI

Comparative genomics of the lactic acid bacteria

TL;DR: Phylogenetic analyses, comparison of gene content across the group, and reconstruction of ancestral gene sets indicate a combination of extensive gene loss and key gene acquisitions via horizontal gene transfer during the coevolution of lactic acid bacteria with their habitats.
Journal ArticleDOI

Genomic analysis of Oenococcus oeni PSU-1 and its relevance to winemaking

TL;DR: The completion of the Oenococcus oeni genome marks a significant new phase for wine-related research on lactic acid bacteria in which the physiology, genetic diversity and performance of O. oeni starter cultures can be more rigorously examined.
Journal ArticleDOI

Persistence and transferability of noroviruses on and between common surfaces and foods.

TL;DR: In this article, the persistence and transferability of representative noroviruses Norwalk virus (NV), Snow Mountain virus (SMV), and murine norovirus 1 (MNV-1) on and between solid surfaces and foods were characterized.
Journal ArticleDOI

PCR-Based Method Using Propidium Monoazide To Distinguish Viable from Nonviable Bacillus subtilis Spores

TL;DR: A molecular-based method which is able to discriminate between viable and inactivated Bacillus subtilis spores by utilizing the DNA-intercalating dye propidium monoazide is described.
Journal ArticleDOI

A real-time PCR assay for the enumeration and detection of Zygosaccharomyces bailii from wine and fruit juices.

TL;DR: This assay provides a rapid and accurate method to establish the levels of the total Z. bailii population which consists of both viable and nonviable cells.