Part:BBa_K2278021

D-NY15 Antimicrobial peptide with Alpha-Factor Secretion Signal

Sequence and Features

Assembly Compatibility:

• 10
  COMPATIBLE WITH RFC[10]
• 12
  COMPATIBLE WITH RFC[12]
• 21
  INCOMPATIBLE WITH RFC[21]

  Illegal XhoI site found at 244
  
• 23
  COMPATIBLE WITH RFC[23]
• 25
  COMPATIBLE WITH RFC[25]
• 1000
  COMPATIBLE WITH RFC[1000]

Introduction

This DNA biobrick was designed in order to produce an antimicrobial peptide from the crocodile Crocodylus siamensis.

1- Biological background

Antimicrobial peptides (AMP) are phylogenetically ancient components of the innate defense of both invertebrates and vertebrates. In the context of growing bacterial antibiotic-resistance, these AMP are considered as potential new therapeutical candidates.
The D-NY15 construction was based on the small peptide Leucrocin I sequence (NGVQPKY ; Yaraksa et al., 2013). Leucrocin I ((BBa_K2278022) comes from Siamese crocodile white blood cells and shows a good antibacterial activity towards Vibrio cholerae. The sequence of Leucrocin I was improved to enhance the antimicrobial properties which depends on net charge (the AMP binds to a negatively charged membrane), length, structure, and hydrophobic percentage (to insert and permeabilize the microbial membrane). To do that Yaraksa et al added hydrophobic amino acids (A4, L6, F7, V8, F11) and positively charged amino acids (K2, K3, K13) to Leucrocin I sequence. This results in D-NY15 (NKKAGLFVVQFPKKY ; figure 1).

Figure 1: (A) 3D predicted structure of NY-15 antimicrobial peptide modeled on line with Mobyle portal. (B) Example of an AMP model of intracellular killing mechanism : the barrel-stave model of antimicrobial-peptide-induced killing (Brogden, 2005)

The mechanism of action of D-NY15 has been observed by transmission electron microscopy. The AMP binds and inserts to bacterium membranes to create pores, leading to the lysis of the cells (figure 2).

Figure 2: Scanning electron micrographs of Vibrio cholerae treated with peptides (a) control bacteria c) bacteria treated with D-NY15 AMP (Yaraksa et al., 2014)

2- Usage in iGEM projects

The part was designed during the Croc’n Cholera project (team INSA-UPS-France 2017). It contains the coding sequence to produces the D-NY15 AMP with a yeast promoter. The α-factor (BBa_K1800001) sequence contains a RBS and a signal sequence to secrete the produced peptides.

Experiments

1- Molecular biology

The gene was placed under the control of an alpha factor signal. IDT performed the DNA synthesis and delivered the part as gBlock. The construct was cloned by conventional ligation into the pSB1C3 plasmid. The construction was then inserted on plasmid pPICZa and integrated in the yeast genome.

Analysis of the restriction map

Figure 3: Analysis of the restriction map BBa_K2278021. Digested fragments (Xba1 and Pst1) are electrophoresed through a 0.7% agarose gel. The fragment lengths are 2029 bp for pSB1C3 and 300 bp for the required insert.

Sequencing

Figure 4: Sequencing of pSB1C3-D-NY15 1500 ng of plasmid are sequenced. The obtained sequence were blast on the BBa_K2278021 sequence with the iGEM sequencing online tools.

The sequencing successfully validated the sequence of the biobrick.

2- Integration in Pichia pastoris

The biobrick was placedunder the control of the constitutive pGAP promoter (BBa_K431009) and was cloned in the pPICZalpha vector, an expression vector for the yeast Pichia pastoris. The plasmid was then linearized and transferred in Pichia pastoris by electroporation. The integration is predicted to be at the pGAP location. Indeed, the pGAP promoter makes genome recombination easier in Pichia pastoris.

Figure 5: Integration of pGAP+BBa_K2278021 in Pichia pastoris To verify the correct integration, we performed colony PCR and electrophoresed the product through a 0.7% agarose gel. A 850 bp fragment is expected is the integration is correct.

Characterization

D-NY15 production was performed with Pichia pastoris in YPD 40 g/L glucose grown for 4 days at 30 °C with shacking. Cells and supernatants were sampled.

1- Validation of D-NY15 expression in Pichia pastoris by qRT-PCR

RNA from the Pichia pastoris cells were extracted and RT-qPCR was performed (figure 6).

Figure 6 :RTq-PCR of D-NY15 RNA are issued from Pichia pastoris strains with or without the D-NY15 encoding gene

The curves correspond to : A1, A2, A3: Pichia + pPIC-DNY15 ; B1, B2: water control ; C1, C2, C3: Pichia + pPIC (Empty vector). Total RNAs were extracted from transformants and reverse transcriptions were performed using Superscript II reverse transcriptase (Invitrogen) and a reverse primer hybridizing to the 3’ end of DNY15-encoding mRNA. The resulting cDNAs were amplified by quantitative PCR (qPCR). The amount of fluorescence provided by the RTq-PCR with the D-NY15 amorces is raising after 8 cycles whereas the negative control (pPICZalpha only) start to be amplified at 29 cycles (non specific amplification). This mean that the D-NY15 encoding gene is expressed in Pichia pastoris.

Our results show that the mRNA encoding DNY15 can be detected way above the background signal (empty pPIC) in cells transformed with pPIC-DNY15, attesting of the expression of our construct.

2. Toxicity assay

The supernatants of Pichia pastoris strains with or without the D-NY15 encoding gene were used in a halo assay against V. harveyi as the target of AMPs. Briefly, 35mL of supernatants were freeze-dried and then resuspended in 3.5mL of water. A paper cut was soaked with one of these solutions and placed on a petri plate inoculated with V. harveyi (figure 7).

Figure 7 : AMP halo assay Positive control was performed with chloramphenicol (25 g/L), the negative control was performed with the empty plasmid integrated in P. pastoris, the assay is performed with the plasmid containing BBa_K2278021 integrated in P. pastoris.

Conclusion :

Halo are formed around the positive control and the patch containing supernatants from a D-NY15 expressing strain. This nicely demonstrated the capacity of D-NY15 to inhibit the growth of Vibrio harveyi. Here, we show both the capacity of Pichia pastoris to produce antimicrobial peptides and the efficiency of the crocodile peptide D-NY15 to inhibit Vibrio harveyi growth.

Perspectives:

To go further, inhibition test should be now performed in liquid assay to be closer to the conditions in which we want to use these strains.

Design Notes

Part:BBa_K1800001: Alpha-Factor Secretion Signal

Source

The peptides DNA sequence has been obtained by reverse translation of the amino acid sequence of the D-NY15 proposed by Yaraksa et al., 2013, which was determined by mass spectrometry analysis.

References

Yaraksa, N., Anunthawan, T., Theansungnoen, T., Daduang, S., Araki, T., Dhiravisit, A. and Thammasirirak, S. (2013). Design and synthesis of cationic antibacterial peptide based on Leucrocin I sequence, antibacterial peptide from crocodile (Crocodylus siamensis) white blood cell extracts. The Journal of Antibiotics, 67(3), pp.205-212.

Brogden KA (2005) Antimicrobial peptides: pore formers or metabolic inhibitors in bacteria. Nat Rev Microbiol. 3:238-50.