Difference between revisions of "Team:Montpellier/Peptides"

 
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<h1> Peptides </h1>
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<img class="banniere" src="https://static.igem.org/mediawiki/2018/8/8e/T--Montpellier--banniere_peptides.png"/>
  
<h2> Introduction </h2>
+
<section>
 +
 
 +
<h2> Introduction </h2><hr/>
  
 
<p>Antimicrobial peptides have an action against different types of bacteria: but what about the vaginal cells and the vaginal flora ?
 
<p>Antimicrobial peptides have an action against different types of bacteria: but what about the vaginal cells and the vaginal flora ?
It’s has been shown that most of antimicrobials peptides (AMPs) are hydrophobics and cationics peptides, they bind to the anionic phospholipids on the outer surface of bacterial cell membrane [1]. The affinity for the mammalian cells is on the contrary really low because the outer surface is composed of zwitterionic phospholipids. As a consequence, AMPs will not hurt the vaginal epithelial cells. Moreover, AMPs have an higher affinity for spermatozoa membranes which are composed of anionic phospholipids such as phosphatidylglycerol and phosphatidylserine in the plasma membrane, and caused the lost of motility of spermatozoa and prevent the fecondation. Lastly, all the AMPs studied are not harmful for the lactobacilli in the vaginal microbiota [2]. All of this reasons make some AMPs promising targets for being used for contraception.</p>
+
It’s has been shown that most of antimicrobials peptides (AMPs) are hydrophobics and cationics peptides, they bind to the anionic phospholipids on the outer surface of bacterial cell membrane <a class="lien" href="#references">[1]</a>. The affinity for the mammalian cells is on the contrary really low because the outer surface is composed of zwitterionic phospholipids. As a consequence, AMPs will not hurt the vaginal epithelial cells. Moreover, AMPs have an higher affinity for spermatozoa membranes which are composed of anionic phospholipids such as phosphatidylglycerol and phosphatidylserine in the plasma membrane, and caused the lost of motility of spermatozoa and prevent the fecondation. Lastly, all the AMPs studied are not harmful for the <i>Lactobacilli</i> in the vaginal microbiota <a class="lien" href="#references">[2]</a>. All of this reasons make some AMPs promising targets for being used for contraception.</p>
  
<h2>The different AMPs </h2>
+
<h2>The different AMPs</h2><hr/>
<h3>Subtilosin A </h3>
+
<p>Subtilosin A (SboA) is an antimicrobial peptide of 32 amino acids naturally produced by Bacillus subtilis.
+
This AMP is a very good candidate since it also is involved in various antimicrobial activity against pathogenic organisms such as Gardnerella vaginalis [3] involved in Bacterial vaginosis. </p>
+
  
<p>SboA is produced and then secreted by B. subtitles thanks to a very complex operon made of 8 genes called the Alb operon. (figure 1)</p>
+
<h3>LL37</h3>
<p><img src="https://static.igem.org/mediawiki/2018/7/75/T--Montpellier--subtilosin_Montpellier.png">
+
<fig caption>Figure 1 : The alb operon</fig caption></p>
+
<h4>Production of Subtilosin A </h4>
+
<p>In Bacillus subtilis, the subtilosin A is produced by the expression of an operon of 8 genes (figure 1).
+
However, It is possible to get a correctly folded - and therefore active - protein with only SboA and AlbA genes [4].
+
Indeed, SboA is the Subtilosin A precursor of 32 amino acids, and Alba is part of radical SAM proteins superfamily proteins that use [4Fe-4S]+ cluster to reductively cleave S-adenosyl-L-methionine (SAM) to generate a radical and catalyze the formation of 3 thioether bonds in SboA making it mature.</p>
+
<h4>Iron Sulfur Cluster Complementation</h4>
+
<p>It’s known that the production of mature SboA is more efficient when the SUF genes (Iron Sulfur Cluster) are added to the host organism. It is due to the [4Fe-4S]+ cluster, a cofactor of AlbA. [4]
+
  
These SUF genes are expressed by numerous prokaryotic cells under stress conditions.
 
And this is no exception of B. subtilis. Also, to make sure that our peptide is well produced and in a sufficient amount, we added the suf genes of B. subtilis to our construction, so that the cluster is produced even in non stressing conditions.</p>
 
<h3>Lacticin 3147</h3>
 
<p>This Class I bacteriocin is composed by two peptides lantibiotic: Ltn⍺ and Ltnꞵ. (Figure 2). It’s produced by Lactoccocus lactis subsp. lactis [5]. This bacterium contains a 60,232 bp conjugative plasmide, pMRC01 which presents the 6 gene cluster (ltnA1, A2, M1, T and M2) to synthesize lacticin 3147 [6].</p>
 
 
<p><img src="https://static.igem.org/mediawiki/2018/3/3c/T--Montpellier--lacticin_Montpellier.JPG"><br>
 
<fig caption> Figure 2 : Lacticin 3147 structure. LtnA1 and LtnA2 peptides in their mature active form.
 
“Carine Dortu & Philippe Thonart : Bacteriocins from lactic acid bacteria: interest for food products biopreservation.”
 
</fig caption></p>
 
<p><i>ltnA1</i> and <i>ltnA2</i> encode LtnA1 and LtnA2 who in their mature active form are termed Ltn⍺ and Ltnꞵ. It was study that ltnM1 and ltnM2 show homology to genes involved in the production and export of lantibiotics. That’s why we used ltnA1, ltnA2, ltnM1 and ltnM2 in our circuit [7].
 
Some experiments have proved lacticin exhibit spermicidal activity against horse/pony, bovine, boar and rat sperm immobilizing them within 30 s by using peptides LtnA1 and Ltn2 together [3].</p>
 
 
<h3>LL37</h3>
 
 
<p>LL-37 is an antimicrobial peptide from human macrophages and leukocytes. It is the only member from the human cathelicidin family. This peptide appears to have very important spermicidal effects.  
 
<p>LL-37 is an antimicrobial peptide from human macrophages and leukocytes. It is the only member from the human cathelicidin family. This peptide appears to have very important spermicidal effects.  
“Human cathelicidin LL-37 is the most promising spermicidal AMP to be further developed for vaginal use” [2]
+
“Human cathelicidin LL-37 is the most promising spermicidal AMP to be further developed for vaginal use” <a class="lien" href="#references">[2]</a>
 
LL-37 has shown effect in vivo in mice. Females naturally cycling to estrous phase failed to become pregnant when in injected with LL-37 and sperm. LL-37 also showed in vitro effect on human sperm which makes it a very good potential peptide for contraception. The fact that this peptide is naturally produced by human and moreover in the vagina after intercourse adds to the peptide the proof of harmlessness for the vaginal flora.
 
LL-37 has shown effect in vivo in mice. Females naturally cycling to estrous phase failed to become pregnant when in injected with LL-37 and sperm. LL-37 also showed in vitro effect on human sperm which makes it a very good potential peptide for contraception. The fact that this peptide is naturally produced by human and moreover in the vagina after intercourse adds to the peptide the proof of harmlessness for the vaginal flora.
 
Lastly this peptide is only 37 amino acids long so it is easy to produce and doesn’t need post translational modification.</p>
 
Lastly this peptide is only 37 amino acids long so it is easy to produce and doesn’t need post translational modification.</p>
  
<h2>Design</h2>
+
<h3>Subtilosin A</h3>
  
 +
<p>Subtilosin A (SboA) is an antimicrobial peptide of 32 amino acids naturally produced by <i>Bacillus subtilis</i>.
 +
This AMP is a very good candidate since it also is involved in various antimicrobial activity against pathogenic organisms such as Gardnerella vaginalis <a class="lien" href="#references">[3]</a> involved in bacterial vaginosis.</p>
  
<h3>General design</h3>
+
<p>SboA is produced and then secreted by <i>B. subtilis</i> thanks to a very complex operon made of 8 genes called the <strong>Alb operon</strong> (Figure 1).</p>
<p>Each of our constructions contained rpsU promoter [8] which is a Lactobacillus jensenii strong promoter.  This RpsU sequence also contains the putative sequence for the RBS
+
We added spacers to all of our constructions to unable easier use of the sequence and separation of the different genes of the sequences. We used two Terminators to our sequences :BBa_B0014 & BBa_B0015 to ensure the stopping of the transcription.
+
Our constructions were assembled in the Plem415 vector by Gibson Assembly method. Plem 415 is a plasmid that works in Lactobacilli species but it’s not specific to L. jensenii [9]
+
</p>
+
<h3>SubtilosinA</h3>
+
<p><img class="design" src="https://static.igem.org/mediawiki/2018/2/25/T--Montpellier--subtilosin_design_Montpellier.png"><br>
+
<fig caption>Figure 3 : Design of the sequence coding the Subtilosin protein with the RpsU promoter.</fig caption>
+
<img src="https://static.igem.org/mediawiki/2018/2/25/T--Montpellier--subtilosin_suf_design_Montpellier.png"><br>
+
<fig caption>Figure 4 : Design of the sequence coding the Iron Sulfur Cluster with the RpsU promoter.</fig caption></p>
+
<h3>Lacticin 3147</h3>
+
<p>This circuit was made from 2 native genes of Lactococcus Lactis ltA1 and ltnA that express Lacticin peptide. Also, the design contains Lacticin-post-transcriptional regulator ltM1 and M2. A promoter orthogonal was used : ptsH and differents spacer taken from igem_parts.</p>
+
<img src="https://static.igem.org/mediawiki/2018/9/95/T--Montpellier--lacticin_design_Montpellier.png">
+
  
<h3>LL-37</h3>
+
<figure><img class="sub" src="https://static.igem.org/mediawiki/2018/7/75/T--Montpellier--subtilosin_Montpellier.png"><br/>
 +
<figcaption><span class="underline">Figure 1:</span> The alb operon.</figcaption>
 +
</figure>
  
<p>The design of LL-37 is simpler than the one of the other peptides. Indeed, the protein is coded only with the well-named gene LL-37.</p>
+
<h4>Production of Subtilosin A</h4>
  
<img src="https://static.igem.org/mediawiki/2018/3/36/T--Montpellier--LL37_design_Montpellier.png">
+
<p>In <i>B. subtilis</i>, the subtilosin A is produced by the expression of an operon of 8 genes Ffigure 1).
<img src="https://static.igem.org/mediawiki/2018/2/20/T--Montpellier--LL372_design_Montpellier.png">
+
However, It is possible to get a correctly folded - and therefore active - protein with only SboA and AlbA genes <a class="lien" href="#references">[4]</a>.  
 +
Indeed, <strong>SboA</strong> is the Subtilosin A precursor of 32 amino acids, and <strong>Alba</strong> is part of radical SAM proteins superfamily proteins that use [4Fe-4S]+ cluster to reductively cleave S-adenosyl-L-methionine (SAM) to generate a radical and catalyze the formation of 3 thioether bonds in SboA making it mature.</p>
 +
<h4>Iron Sulfur Cluster Complementation</h4>
 +
<p>It’s known that the production of mature SboA is more efficient when the SUF genes (Iron Sulfur Cluster) are added to the host organism. It is due to the [4Fe-4S]+ cluster, a cofactor of AlbA <a class="lien" href="#references">[4]</a>.
  
 +
These SUF genes are expressed by numerous prokaryotic cells under stress conditions.
 +
And this is no exception of <i>B. subtilis</i>. Also, to make sure that our peptide is well produced and in a sufficient amount, we added the suf genes of <i>B. subtilis</i> to our construction, so that the cluster is produced even in non stressing conditions.</p>
  
 +
<h3>Lacticin 3147</h3>
  
 +
<p>This Class I bacteriocin is composed by two peptides lantibiotic: Ltn⍺ and Ltnbeta. It’s produced by <i>Lactoccocus lactis subsp. lactis</i> <a class="lien" href="#references">[5]</a>. This bacterium contains a 60,232 bp conjugative plasmide, pMRC01 which presents the 6 gene cluster (ltnA1, A2, M1, T and M2) to synthesize lacticin 3147 <a class="lien" href="#references">[6]</a>.</p>
  
</section>
 
</body>
 
  
 +
<p><i>ltnA1</i> and <i>ltnA2</i> encode LtnA1 and LtnA2 who in their mature active form are termed Ltn⍺ and Ltnꞵ. It was study that ltnM1 and ltnM2 show homology to genes involved in the production and export of lantibiotics. That’s why we used ltnA1, ltnA2, ltnM1 and ltnM2 in our circuit <a class="lien" href="#references">[7]</a>.
 +
Some experiments have proved lacticin exhibit spermicidal activity against horse/pony, bovine, boar and rat sperm immobilizing them within 30 s by using peptides LtnA1 and Ltn2 together.</p>
  
 +
<h3> Nisin </h3>
  
 +
 +
<p> Nisin, a 34 amino acid cationic peptide, is a member of the lantibiotic family known to be produced by bacteria, Lactococcus lactis. The encoded precursor is 57 amino acids long, with a 23-residue leader region and a 34-residue structural region. </p>
 +
 +
<p> Thus, the protein Nisin is an effective spermicidal compound with a dose- and time-dependent effect. At a 300–400-g dose, complete immobilization of human spermatozoa was observed within 20 s. Moreover, we know that if we add Nisin in mice during 14 days, we do not see abnormalities in cycle or morphology of the vaginal epithelial cells, inflammatory reaction(s) in the vaginal epithelium <a class="lien" href="#references">[8]</a> . However we don’t know how the Nisin immobilize sperm. </p>
 +
 +
</section>
  
 
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<section class="references" id="references">
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     <tr>
 
       <td class="references_left">[1]</td>
 
       <td class="references_left">[1]</td>
       <td class="references_right">Rajesh K. Naz, Subhash C.Chauhan. 2001. Presence of antibodies to sperm YLP12 synthetic peptide in sera and seminal plasma of immunoinfertile men. <i>Molecular Human Reproduction</i> Vol.7 no.1 pp. 21–26.</td>
+
       <td class="references_right">Nguyen LT1, Haney EF, Vogel HJ. (2011). The expanding scope of antimicrobial peptide structures and their modes of action. <i>Trends Biotechnol</i> Vol 29, 464–472..</td>
 
     </tr>
 
     </tr>
 
     <tr>
 
     <tr>
 
       <td class="references_left">[2]</td>
 
       <td class="references_left">[2]</td>
       <td class="references_right">Rajesh K. Naz. 2014. Vaccine for human contraception targeting sperm Izumo protein and YLP12 dodecamer peptide. <i>Protein Science</i> 2014 Vol.23:857—868.</td>
+
       <td class="references_right">Tanphaichitr, Nongnuj et al. (2018). Potential Use of Antimicrobial Peptides as Vaginal Spermicides/Microbicides. <i>Pharmaceuticals</i> 9.1 (2016): 13.</td>
 
     </tr>
 
     </tr>
 
     <tr>
 
     <tr>
 
       <td class="references_left">[3]</td>
 
       <td class="references_left">[3]</td>
       <td class="references_right">A.S. Samuel and R.K. Naz. 2008. Isolation of human single chain variable fragment antibodies against specific sperm antigens for immunocontraceptive development. <i>Human Reproduction</i> Vol.23, No.6 pp. 1324–1337.</td>
+
       <td class="references_right">Cavera, V. L., Volski, A., & Chikindas, M. L. (2015). The natural antimicrobial subtilosin A synergizes with lauramide arginine ethyl ester (LAE), ε-poly-l-lysine (polylysine), clindamycin phosphate and metronidazole, against the vaginal pathogen Gardnerella vaginalis. <i>Probiotics and antimicrobial proteins.</i> 7(2), 164-171.</td>
 
     </tr>
 
     </tr>
 
     <tr>
 
     <tr>
 
       <td class="references_left">[4]</td>
 
       <td class="references_left">[4]</td>
       <td class="references_right">Angela Marcobal, Xiaowen Liu, Wenlei Zhang, Antony S. Dimitrov, Letong Jia, Peter P. Lee, Timothy R. Fouts, Thomas P. Parks, and Laurel A. Lagenaur. 2016. Expression of Human Immunodeficiency Virus Type 1 Neutralizing Antibody Fragments Using Human Vaginal <i>Lactobacillus</i>. <i>Aids Resaerch And Human Retroviruses</i> Volume 32, Number 10/11.</td>
+
       <td class="references_right">Paul M. Himes, Scott E. Allen, Sungwon Hwang, and Albert A. Bowers. (2016).Production of Sactipeptides in Escherichia coli: Probing the Substrate Promiscuity of Subtilosin A Biosynthesis. <i>ACS Chemical Biology</i>. 11 (6), 1737-1744.</td>
 
     </tr>
 
     </tr>
 
     <tr>
 
     <tr>
 
       <td class="references_left">[5]</td>
 
       <td class="references_left">[5]</td>
       <td class="references_right">Xiaowen Liu, Laurel A. Lagenaur, David A. Simpson, Kirsten P. Essenmacher, Courtney L. Frazier-Parker, Yang Liu, Daniel Tsai, Srinivas S. Rao, Dean H. Hamer, Thomas P. Parks, Peter P. Lee and Qiang Xu. 2006. Engineered Vaginal <i>Lactobacillus</i> Strain for Mucosal Delivery of the Human Immunodeficiency Virus Inhibitor Cyanovirin-N. <i>Antimicrob Agents Chemother</i> Vol. 50, No. 10, p. 3250–3259</td>
+
       <td class="references_right">Srinivas Suda et al., (2012). Lacticin 3147 - Biosynthesis, Molecular Analysis, Immunity, Bioengineering and Applications. Current Protein & Peptide Science <i>Antimicrob Agents Chemother</i> volume 13, pages 193-204.</td>
 
     </tr>
 
     </tr>
    <tr>
+
      <tr>
       <td class="references_bottom_left">[6]</td>
+
       <td class="references_left">[6]</td>
       <td class="references_bottom_right">Fridy, P. C., Li, Y., Keegan, S., Thompson, M. K., Nudelman, I., Scheid, J. F., ... & Rout, M. P. 2014. A robust pipeline for rapid production of versatile nanobody repertoires. <i>Nature methods</i>, 11(12), 1253.</td>
+
       <td class="references_right">Dougherty et al., (1998). Sequence and analysis of the 60 kb conjugative, bacteriocin-producing plasmid pMRC01 from Lactococcus lactis DPC3147 <i>Mol. Microbiol.</i> 29 (4), 10291038</td>
 +
    </tr>
 +
            <tr>
 +
      <td class="references_left">[7]</td>
 +
      <td class="references_right">Silkin, L. et al., (2008). Spermicidal bacteriocins: Lacticin 3147 and subtilosin A <i>Bioorganic & Medicinal Chemistry Letters</i> 18  3103–3106 Spermicidal</td>
 +
    </tr>
 +
  <tr>
 +
      <td class="references_left">[8]</td>
 +
      <td class="references_right">K V R Reddy, C Aranha, S M Gupta and R D Yedery. (2004). Evaluation of antimicrobial peptide nisin as a safe vaginal contraceptive agent in rabbits: in vitro and in vivo studies. <i> Reproduction</i> Volume 128. Page(s): 117–126.</td>
 
     </tr>
 
     </tr>
 
   </table>
 
   </table>
 +
 +
</section>
 +
 +
</body>
 +
 
</html>
 
</html>
  

Latest revision as of 21:30, 16 October 2018

Peptides

Introduction


Antimicrobial peptides have an action against different types of bacteria: but what about the vaginal cells and the vaginal flora ? It’s has been shown that most of antimicrobials peptides (AMPs) are hydrophobics and cationics peptides, they bind to the anionic phospholipids on the outer surface of bacterial cell membrane [1]. The affinity for the mammalian cells is on the contrary really low because the outer surface is composed of zwitterionic phospholipids. As a consequence, AMPs will not hurt the vaginal epithelial cells. Moreover, AMPs have an higher affinity for spermatozoa membranes which are composed of anionic phospholipids such as phosphatidylglycerol and phosphatidylserine in the plasma membrane, and caused the lost of motility of spermatozoa and prevent the fecondation. Lastly, all the AMPs studied are not harmful for the Lactobacilli in the vaginal microbiota [2]. All of this reasons make some AMPs promising targets for being used for contraception.

The different AMPs


LL37

LL-37 is an antimicrobial peptide from human macrophages and leukocytes. It is the only member from the human cathelicidin family. This peptide appears to have very important spermicidal effects. “Human cathelicidin LL-37 is the most promising spermicidal AMP to be further developed for vaginal use” [2] LL-37 has shown effect in vivo in mice. Females naturally cycling to estrous phase failed to become pregnant when in injected with LL-37 and sperm. LL-37 also showed in vitro effect on human sperm which makes it a very good potential peptide for contraception. The fact that this peptide is naturally produced by human and moreover in the vagina after intercourse adds to the peptide the proof of harmlessness for the vaginal flora. Lastly this peptide is only 37 amino acids long so it is easy to produce and doesn’t need post translational modification.

Subtilosin A

Subtilosin A (SboA) is an antimicrobial peptide of 32 amino acids naturally produced by Bacillus subtilis. This AMP is a very good candidate since it also is involved in various antimicrobial activity against pathogenic organisms such as Gardnerella vaginalis [3] involved in bacterial vaginosis.

SboA is produced and then secreted by B. subtilis thanks to a very complex operon made of 8 genes called the Alb operon (Figure 1).


Figure 1: The alb operon.

Production of Subtilosin A

In B. subtilis, the subtilosin A is produced by the expression of an operon of 8 genes Ffigure 1). However, It is possible to get a correctly folded - and therefore active - protein with only SboA and AlbA genes [4]. Indeed, SboA is the Subtilosin A precursor of 32 amino acids, and Alba is part of radical SAM proteins superfamily proteins that use [4Fe-4S]+ cluster to reductively cleave S-adenosyl-L-methionine (SAM) to generate a radical and catalyze the formation of 3 thioether bonds in SboA making it mature.

Iron Sulfur Cluster Complementation

It’s known that the production of mature SboA is more efficient when the SUF genes (Iron Sulfur Cluster) are added to the host organism. It is due to the [4Fe-4S]+ cluster, a cofactor of AlbA [4]. These SUF genes are expressed by numerous prokaryotic cells under stress conditions. And this is no exception of B. subtilis. Also, to make sure that our peptide is well produced and in a sufficient amount, we added the suf genes of B. subtilis to our construction, so that the cluster is produced even in non stressing conditions.

Lacticin 3147

This Class I bacteriocin is composed by two peptides lantibiotic: Ltn⍺ and Ltnbeta. It’s produced by Lactoccocus lactis subsp. lactis [5]. This bacterium contains a 60,232 bp conjugative plasmide, pMRC01 which presents the 6 gene cluster (ltnA1, A2, M1, T and M2) to synthesize lacticin 3147 [6].

ltnA1 and ltnA2 encode LtnA1 and LtnA2 who in their mature active form are termed Ltn⍺ and Ltnꞵ. It was study that ltnM1 and ltnM2 show homology to genes involved in the production and export of lantibiotics. That’s why we used ltnA1, ltnA2, ltnM1 and ltnM2 in our circuit [7]. Some experiments have proved lacticin exhibit spermicidal activity against horse/pony, bovine, boar and rat sperm immobilizing them within 30 s by using peptides LtnA1 and Ltn2 together.

Nisin

Nisin, a 34 amino acid cationic peptide, is a member of the lantibiotic family known to be produced by bacteria, Lactococcus lactis. The encoded precursor is 57 amino acids long, with a 23-residue leader region and a 34-residue structural region.

Thus, the protein Nisin is an effective spermicidal compound with a dose- and time-dependent effect. At a 300–400-g dose, complete immobilization of human spermatozoa was observed within 20 s. Moreover, we know that if we add Nisin in mice during 14 days, we do not see abnormalities in cycle or morphology of the vaginal epithelial cells, inflammatory reaction(s) in the vaginal epithelium [8] . However we don’t know how the Nisin immobilize sperm.

References
[1] Nguyen LT1, Haney EF, Vogel HJ. (2011). The expanding scope of antimicrobial peptide structures and their modes of action. Trends Biotechnol Vol 29, 464–472..
[2] Tanphaichitr, Nongnuj et al. (2018). Potential Use of Antimicrobial Peptides as Vaginal Spermicides/Microbicides. Pharmaceuticals 9.1 (2016): 13.
[3] Cavera, V. L., Volski, A., & Chikindas, M. L. (2015). The natural antimicrobial subtilosin A synergizes with lauramide arginine ethyl ester (LAE), ε-poly-l-lysine (polylysine), clindamycin phosphate and metronidazole, against the vaginal pathogen Gardnerella vaginalis. Probiotics and antimicrobial proteins. 7(2), 164-171.
[4] Paul M. Himes, Scott E. Allen, Sungwon Hwang, and Albert A. Bowers. (2016).Production of Sactipeptides in Escherichia coli: Probing the Substrate Promiscuity of Subtilosin A Biosynthesis. ACS Chemical Biology. 11 (6), 1737-1744.
[5] Srinivas Suda et al., (2012). Lacticin 3147 - Biosynthesis, Molecular Analysis, Immunity, Bioengineering and Applications. Current Protein & Peptide Science Antimicrob Agents Chemother volume 13, pages 193-204.
[6] Dougherty et al., (1998). Sequence and analysis of the 60 kb conjugative, bacteriocin-producing plasmid pMRC01 from Lactococcus lactis DPC3147 Mol. Microbiol. 29 (4), 10291038
[7] Silkin, L. et al., (2008). Spermicidal bacteriocins: Lacticin 3147 and subtilosin A Bioorganic & Medicinal Chemistry Letters 18 3103–3106 Spermicidal
[8] K V R Reddy, C Aranha, S M Gupta and R D Yedery. (2004). Evaluation of antimicrobial peptide nisin as a safe vaginal contraceptive agent in rabbits: in vitro and in vivo studies. Reproduction Volume 128. Page(s): 117–126.