Tier 4SS-0616Bean CounterSoybean

Natto Fury

G. max · Bean heat

Scoville Splice Natto Fury (SS-0616) — engineered Soybean specimen on-plant with laboratory specimen tag

Scoville Heat Units

7,483

0
16M

0.0% of pure capsaicin

This is a computed design target (0.0% of pure-capsaicin concentration), derived from the flux model and blend chemistry — not a measured value. It sits within concentrations measured in real peppers. See the evidence behind it:

Genes

12

Construct

18,540 bp

Variant

Triple

Promoter

seed-specific

Technical Manifest

Construct Type

T-DNA binary vector

Selection Marker

nptII (kanamycin resistance)

Codon Optimization

legume

Capsaicinoid Profile

Standard

Gene Cassettes (10)

pAMT expression cassettevanillylamine biosynthesis
Pun1/CS (Triple) expression cassettecapsaicin synthase
BCAT expression cassettepathway enzyme
KAS expression cassettepathway enzyme
FAR expression cassettepathway enzyme
PAL expression cassettepathway enzyme
C4H expression cassettepathway enzyme
4CL expression cassettepathway enzyme
HCT expression cassettepathway enzyme
COMT expression cassettepathway enzyme

Construct map

18,540 bp · T-DNA binary vector
Left Border (LB) · 78 bp
nptII selection cassette · 795 bp
pAMT expression cassette
Pun1/CS (Triple) expression cassette
BCAT expression cassette
KAS expression cassette
FAR expression cassette
PAL expression cassette
C4H expression cassette
4CL expression cassette
HCT expression cassette
COMT expression cassette
Right Border (RB) · 75 bp

Burn Profile

Bean heat

Onset 4s
Peak 18s
Duration 2m
Profile Whisper

Specimen library

Organism documentation

Scoville Splice Soybean on-plant hero research specimen

On-plant

Scoville Splice Soybean cross-section research specimen

Cross-section

Scoville Splice Soybean clinical specimen research specimen

Clinical specimen

About this design

Natto Fury is an engineered G. max construct targeting 7.5K SHU — a Bean Counter Series design in the Tier 4 tier. Bean heat

The construct is 18,540 bp, carrying 12 gene cassettes. T-DNA binary vector with legume-native codon optimization. Selection marker: nptII (kanamycin resistance).

Package contents

  • FASTA constructAnnotated full-length DNA sequence (18,540 bp) with all cassette boundaries, promoter elements, and selection markers labeled.
  • One-page datasheetVisual lab reference: SHU target, gene cassette diagram, key parameters, and capsaicinoid blend ratio.
  • Technical manifestMachine-readable JSON with full construct specification: component list, selection marker, codon optimization, and capsaicinoid profile.
  • Flux balance analysisComplete FBA model output underlying the SHU design target: pathway flux predictions, reaction constraints, and metabolic network assumptions.
  • CRISPR guide designsGuide RNA sequences for cassette integration loci, with Tm values, GC content, off-target risk scores, and integration confirmation primers.
  • Plasmid mapCircular diagram, proportionally scaled, with all components labeled by position and function.
  • Transformation protocolStep-by-step guide for introducing this construct into G. max: selection conditions, tissue preparation, and PCR-based screening strategy.

Delivered instantly

From $510

How to use this

This construct is packaged for introduction into G. max. The transformation protocol covers the complete procedure for this host:

  1. 1

    Prepare the expression system

    This construct is packaged as a T-DNA binary vector for introduction into G. max. See the transformation protocol for delivery method and host preparation details.

  2. 2

    Transform Soybean

    Introduce the construct using the method specified in the protocol. Delivery conditions are specific to G. max tissue competency and the construct's integration requirements.

  3. 3

    Select with nptII (kanamycin resistance)

    Propagate on selection medium at conditions given in the protocol. Non-transformed lines will not survive.

  4. 4

    Screen and advance

    Confirm integration using the primers included in the CRISPR guide designs. Advance confirmed transformants to the appropriate developmental stage to assess capsaicinoid expression.

License this cultivar

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Take it further with CRISPR

The CRISPR guide designs in this package are ready to use with Cas9 or Cpf1 for precision integration at defined genomic loci — and for disrupting competing pathway enzymes that reduce capsaicinoid yield. For site-specific insertion, pathway stacking, or multiplexed editing across soybean cultivars, the guides are your starting point.

Work with Scoville Splice

This construct is a research tool. What it can become is an ingredient.

Scoville Splice works with food and beverage companies to take engineered capsaicinoid constructs from sequence to supply chain. If you’re developing a product — a sauce, a seasoning, a functional food — and you need a precise, consistent heat profile that no natural soybean can deliver, that’s what we were built for. We offer custom cultivar development, strain characterization, pilot-scale grow protocols, and formulation consulting.

Contact us about a partnership →

Already licensed?

Common questions

What is the target SHU of Natto Fury?

Natto Fury is engineered to a target of 7,483 Scoville Heat Units. Burn character: Bean heat. Capsaicinoid profile: -.

What host organism does Natto Fury use?

Natto Fury is a Tier 4 cultivar in the Bean Counter series, built on Soybean (G. max). The construct runs 12 genes across 18,540 base pairs, driven by the seed-specific promoter system.

What license tiers are available for Natto Fury?

Every catalog cultivar can be licensed at Specimen (one SKU, non-exclusive) or Sector (industry-sector exclusive) tiers. Genome and Platform licensing are available on request for category or stack-wide deals. See the licensing page for pricing structure.

What is included in the Natto Fury download package?

The Natto Fury bundle contains the full construct FASTA, a JSON manifest (gene list, promoter stack, codon-optimization notes), the FBA predictions, computationally designed CRISPR guide RNAs, the datasheet, a short product paper, and a signed ZIP for provenance.

Related reading

From the Scoville Splice journal

Often licensed together

All 10 in series →