Part:BBa_K2924051

Leaderless 'TesA

Rhamnose-inducible promoter (similar to BBa_K914003) and RBS* (BBa_K2924009¹) expressing the thioesterase tesA (BBa_K1472601)and a double terminator (BBa_B0015).

Usage and Biology

This part contains the rhamnose-inducible promoter P_rha described by Kelly et al. (2018)^-1 which was further modified by Behle et al. (2019)⁰, and is similar to (BBa_K914003), the RBS* (BBa_K2924009)¹, a thioesterase from Escherichia coli (BBa_K1472601) and a double terminator (BBa_B0015).

In general, all basic parts used here (with the exception of ‘TesA) were optimized for Synechocystis sp. PCC 6803, but function efficiently in both E. coli and Synechocystis sp..

This thioesterase lacks a leader peptide sequence, which is the N-terminal 26-amino acid signal peptide sequence. ’TesA is located in the cytosol of E.coli, where it hydrolyzes the bond of fatty acyl to acyl-carrier protein (ACP) or Coenzyme A (CoA). This results in a free fatty acids and either ACP or CoA.

Background

Fig. 1: Structural formula of hexadecanoic acid. Gray spheres represent a carbon atom, red spheres represent oxygen atom and the white spheres represent hydrogen atoms.

Fig. 2: Structural formula of octadecanoic acid. Gray spheres represent a carbon atom, red spheres represent oxygen atom and the white spheres represent hydrogen atoms.

Fatty acids are long aliphatic chained carboxylic acids, which can be saturated or unsaturated. They have mostly an even number of carbon atoms from 4 to 28. Hexadecanoic acid (Fig. 1) is a saturated long-chain fatty acid, which contains 16 carbon-atoms and is also called palmitic acid (C16:0). It has a white or colorless crystalline form and a slightly characteristic odor². It has a molecular weight of 256.42 g/mol.

Octadecanoic acid (Fig. 2) is a saturated long-chain fatty acid, which contains 18 carbon-atoms and is also called stearic acid (C18:0). It is a white or slightly yellow, wax-like solid with mild odor³. It has a molecular weight of 284.48 g/mol.

Usage of palmitic and stearic acid

The long-chain fatty acid palmitic acid (C16:0) is found naturally in human milk, in cow's milk fat for triglycerides or in vegetable oils and it is commonly used in infant formulas⁴. It is the most abundant fatty acid in cow’s milk⁵.

Palmitic acid (C16:0) is an important chemical, which is used to make soaps or cosmetics agents, lubricating oils, waterproofing materials, food additives and other chemicals².

Stearic acid (C18:0) is also found naturally in animal milk and vegetable oils³ and used in manufacturing of different pharmaceuticals, cosmetics, soaps, candles, food packaging, modeling compounds and other chemicals. It is found sometimes in pesticides³.

Moreover, they play an important role for the intracellular biological functions. They mainly serve as source of metabolic energy or as substrates for the cell membrane biosynthesis. Another function is serving as precursor, such as prostaglandins (PGs), leukotrienes and more, for different signaling pathways⁵. It has been shown that saturated fatty acids, such as palmitic and stearic acid (C16:0; C18:0), induce apoptosis of human granulosa cells, which could be used for further medical investigations⁵. Both fatty acids are used for special dietary to increase the milk fat yield and as an energy source for milk production⁶.

Sequence and Features

Assembly Compatibility:

• 10
  COMPATIBLE WITH RFC[10]
• 12
  COMPATIBLE WITH RFC[12]
• 21
  COMPATIBLE WITH RFC[21]
• 23
  COMPATIBLE WITH RFC[23]
• 25
  COMPATIBLE WITH RFC[25]
• 1000
  COMPATIBLE WITH RFC[1000]

Characterization

First, the inducible promoter, as well as the terminator with Gibson overhangs were fused to ‘tesA via overlap extension PCR. This PCR product was used for Gibson assembly to ligate it into the pSNDY backbone. The conjugative shuttle vector pSNDY is a pSHDY⁷ derivative, encoding a nourseothricin resistance instead of spectinomycin, and is a broad-host-range vector able to self-replicate in E. coli, as well as to be transferred to other hosts such as cyanobacteria via conjugation.

Fig. 3: Transformants differ in morphology. <i>E. coli BL21 control transformation (left) and E. coli BL21 transformed with pSNDY containing P_rha:’tesA (right).</i>

After transformation of the P_rha:’tesA construct, the transformants of E. coli BL21 seem to differ in morphology (Figure 3).

With the help of E. coli DH5α transformed with the ‘tesA construct, as well as the helper strain RP4⁸, pSNDY encoding P_rha:’tesA was transferred to Synechocystis sp. via <a href=”https://www.protocols.io/view/triparental-mating-of-synechocystis-ftpbnmn”>conjugation</a>. The effect of ’tesA expression and activity was first tested in vivo with a fatty acid responsive biosensor by detecting the response to intracellular free fatty acids via a reporter protein, and then later by gas chromatography-mass spectrometry (GC-MS).

Biosensor

For a fast and convenient method to detect fatty acids in vivo, the ‘TesA strain was combined with different biosensor constructs containing different promoter and additionally also combined with a construct encoding an Acetyl-CoA carboxylase complex expression cassette (ACC) <a href="https://parts.igem.org/Part:BBa_K2924021">(BBa_K2924021)</a>, which is the rate limiting step of the fatty acid synthesis. E. coli BL21 (DE3) was transformed with various combinations of the different constructs, as shown in Table 1.

Biosensor	Thioesterase	ACC	Antibiotics used
PaldA:eYFP	'tesA	no	Chloramphenicol, CloNat
PAR:sfGFP	'tesA	no	Chloramphenicol, CloNat
PAR:sfGFP	'tesA	yes	Chloramphenicol, CloNat, Ampicillin

The samples were grown in LB-medium with the appropriate antibiotics. The absorption was measured and the samples were diluted to an OD₆₀₀ of 0.5. In addition to the samples, a negative control was included in the experiment. The samples were induced by 1 mM rhamnose and, in the case of ACC overexpression, additionally with 1 mM IPTG. The induced samples were incubated in a 24 well plate at 37°C, which were shaken at 250 rpm. After nearly 16 hours, the samples were taken out of the incubator and transferred on a 96 well plate. Three biological with three technical replicates each were measured. For the analysis, a plate reader was used to measure absorption at a wavelength of 600 nm. The fluorescence was measured at a wavelength of λ_ex/em= 470 / 515 nm for sfGFP as the reporter gene and at a wavelength of λ_ex/em= 497 / 540 nm for eYFP as the reporter gene.

Fig. 5: In vivo P_aldA eYFP biosensor of transformed E. coli cells with and without tesA. The expression of tesA was induced with 1 mM Rhamnose and the cells were incubated for 16 hours.

Figure 5 shows a significant fluorescence response of eYFP, because of the detection of fatty acids by the promoter P_aldA. Compared to the wild type, it can be said that in the induced transformant a clearly higher amount of fatty acids is present. Also compared to the uninduced control, it can be said that the inducible promoter <a href="https://parts.igem.org/Part:BBa_K914003">BBa_K914003</a> is not leaking and works accurate.

P_aldA is known to response to C18:1⁹, therefore this could indicate for the present of the C18:1 fatty acid.

Fig. 6: In vivo P_AR sfGFP biosensor of transformant E. coli cells with and without tesA and the Acetyl-CoA carboxylase (ACC). The expression of tesA was induced with 1 mM Rhamnose and the expression of the ACC complex was induced with 1 mM IPTG. The cells were then incubated for 16 hours.

In figure 6, there is no significant difference in fluorescence response by the biosensor compared to the wild type even compared to the uninsured transformant. The P_AR is known to detect a broad range of medium-chain fatty acids¹⁰, which could indicate that 'TesA does not have a catalytic activity for medium-chain fatty acyl-substrates and therefore, there is no increase in medium-chain fatty acids in the induced transformant.