scholarly journals Distribution of Epsilon-Polylysine Synthetases in Coryneform Bacteria Isolated from Cheese and Human Skin

2020 ◽  
Author(s):  
Xinglin Jiang ◽  
Yulia Radko ◽  
Tetiana Gren ◽  
Emilia Palazzotto ◽  
Tue Sparholt Jørgensen ◽  
...  

ABSTRACTEpsilon-polylysine (ε-PL) is an antimicrobial commercially produced by Streptomyces fermentation and widely used in Asian countries for food preservation. Here we discovered a gene from cheese bacterium Corynebacterium variabile that showed high similarity to the ε-PL synthetase from Streptomyces in terms of enzymatic domain architecture and gene context. By cloning it into Streptomyces coelicolor with a Streptomyces albulus ε-PL synthetase promoter, we confirmed that its product is indeed ε-PL. A comprehensive sequence analysis suggests that ε-PL synthetases are widely spread among coryneform bacteria isolated from cheese and human skin; 14 out of 15 Brevibacterium isolates and 10 out of 12 Corynebacterium isolates contain Pls gene. This discovery raises the possibility that ε-PL as a bioactive secondary metabolite might be produced and play a role in the cheese and skin ecosystems.IMPORTANCEEvery year, microbial contamination causes billions of tons of food wasted and millions of cases of foodborne illness. ε-PL is an excellent food preservative as it is potent, wide spectrum and is heat stable and biodegradable. It has not been accepted by all countries (e.g those in the EU) partially because it was not a natural composition of food but rather originated from the soil bacteria Streptomyces, a famous producer of various antibiotic drugs and toxins. The unexpected finding of ε-PL synthetases in cheese and skin bacteria suggests that ε-PL may naturally exist in cheese and on our skin.

2021 ◽  
Vol 87 (10) ◽  
Author(s):  
Xinglin Jiang ◽  
Yulia Radko ◽  
Tetiana Gren ◽  
Emilia Palazzotto ◽  
Tue Sparholt Jørgensen ◽  
...  

ABSTRACT ε-Poly-l-lysine is a potent antimicrobial produced through fermentation of Streptomyces and used in many Asian countries as a food preservative. It is synthesized and excreted by a special nonribosomal peptide synthetase (NRPS)-like enzyme called Pls. In this study, we discovered a gene from cheese bacterium Corynebacterium variabile that showed high similarity to the Pls from Streptomyces in terms of domain architecture and gene context. By cloning it into Streptomyces coelicolor with a Streptomyces albulus Pls promoter, we confirmed that its product is indeed ε-poly-l-lysine. A comprehensive sequence analysis suggested that Pls genes are widely spread among coryneform actinobacteria isolated from cheese and human skin; 14 out of 15 Brevibacterium isolates and 10 out of 12 Corynebacterium isolates contain it in their genomes. This finding raises the possibility that ε-poly-l-lysine as a bioactive secondary metabolite might be produced and play a role in the cheese and skin ecosystems. IMPORTANCE Every year, microbial contamination causes billions of tons of food wasted and millions of cases of illness. ε-Poly-l-lysine has potent, wide-spectrum inhibitory activity and is heat stable and biodegradable. It has been approved for food preservation by an increasing number of countries. ε-Poly-l-lysine is produced from soil bacteria of the genus Streptomyces, also producers of various antibiotic drugs and toxins and not considered to be a naturally occurring food component. The frequent finding of pls in cheese and skin bacteria suggests that ε-poly-l-lysine may naturally exist in cheese and on our skin, and ε-poly-l-lysine producers are not limited to filamentous actinobacteria.


2010 ◽  
Vol 59 (1) ◽  
pp. 108-114 ◽  
Author(s):  
Robin L. Stingley ◽  
Wen Zou ◽  
Thomas M. Heinze ◽  
Huizhong Chen ◽  
Carl E. Cerniglia

Reduction of Methyl Red (MR) and Orange II (Or II) by 26 human skin bacterial species was monitored by a rapid spectrophotometric assay. The analysis indicated that skin bacteria, representing the genera Staphylococcus, Corynebacterium, Micrococcus, Dermacoccus and Kocuria, were able to reduce MR by 74–100 % in 24 h, with only three species unable to reduce completely the dye in that time. Among the species tested, only Corynebacterium xerosis was unable to reduce Or II to any degree by 24 h, and only Staphylococcus delphini, Staphylococcus sciuri subsp. sciuri and Pseudomonas aeruginosa were able to reduce completely this dye within 24 h. MR reduction started with early-exponential growth in Staphylococcus aureus and Staphylococcus epidermidis, and around late-exponential/early-stationary growth in P. aeruginosa. Reduction of Or II, Ponceau S and Ponceau BS started during late-exponential/early-stationary growth for all three species. Using liquid chromatography/electrospray ionization mass spectrometry analyses, MR metabolites produced by Staph. aureus, Staph. epidermidis and P. aeruginosa were identified as N,N-dimethyl-p-phenylenediamine and 2-aminobenzoic acid. Searches of available genomic and proteomic data revealed that at least four of the staphylococci in this study, Staphylococcus haemolyticus, Staph. epidermidis, Staphylococcus cohnii and Staphylococcus saprophyticus, have hypothetical genes with 77, 76, 75 and 74 % sequence identity to azo1 encoding an azoreductase from Staph. aureus and hypothetical proteins with 82, 80, 72 and 74 % identity to Azo1, respectively. In addition, Staphylococcus capitis has a protein with 79 % identity to Azo1. Western analysis detected proteins similar to Azo1 in all the staphylococci tested, except Staph. delphini, Staph. sciuri subsp. sciuri and Staphylococcus auricularis. The data presented in this report will be useful in the risk assessment process for evaluation of public exposure to products containing these dyes.


PLoS ONE ◽  
2010 ◽  
Vol 5 (12) ◽  
pp. e15829 ◽  
Author(s):  
Niels O. Verhulst ◽  
Rob Andriessen ◽  
Ulrike Groenhagen ◽  
Gabriella Bukovinszkiné Kiss ◽  
Stefan Schulz ◽  
...  

2019 ◽  
Vol 21 (12) ◽  
pp. 4662-4674
Author(s):  
Serge Michalet ◽  
Guillaume Minard ◽  
Wilfried Chevalier ◽  
Guillaume Meiffren ◽  
Yoann Saucereau ◽  
...  

1977 ◽  
Vol 10 (2) ◽  
pp. 161-169 ◽  
Author(s):  
P. D. MARSH ◽  
S. SELWYN
Keyword(s):  

Author(s):  
S. A. Malcolm

SynopsisAn in vivo staining technique has been developed for the demonstration of micro-organisms on human skin. This technique permits the study of the relationship between micro-organisms and the stratum corneum and its associated structures. It also aids an understanding of the factors involved in the nutrition and survival of micro-organisms on the skin surface.In skin sites with large populations of coryneform species the bacteria tend to accumulate at the edges of corneocytes. This tendency is not shared by members of the micrococcaceae.Agar impressions of the skin surface confirm observations of other workers and suggest that the surface of the stratum corneum is composed of domed corneocytes with a network of troughs or channels surrounding them. It is proposed that the association of coryneform bacteria with the edges of corneocytes may be due to the creation of an environment within the troughs which favours microbial colonisation.


2006 ◽  
Vol 110 (5) ◽  
pp. 593-599 ◽  
Author(s):  
J.N. KEARNEY ◽  
EILEEN INGHAM ◽  
W.J. CUNLIFFE ◽  
K. T. HOLLAND
Keyword(s):  

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