Difference between revisions of "Part:BBa K523006"

Revision as of 14:55, 21 July 2015

Plac + LacZ + malS

E. coli periplasmic α-amylase gene malS (see [http://www.ncbi.nlm.nih.gov/nuccore/48994873?from=3735520&to=3737550&report=gbwithparts info from GenBank: U00096.2]) under control of lac promoter. LacZα is also present.

Usage and Biology

While an amylase ought to be capable of degrading starch, the product protein is believed to be periplasmic and thus ought to only degrade starch if it leaks from the periplasm in significant quantities (but see below: this does seem to be the case). Its natural function in E. coli presumably involves degrading shorter glucose chains: [http://dx.doi.org/10.1128/JB.00767-08 Lengsfeld et al (2008)] state that "MalS produces preferentially maltohexaose from longer maltodextrins in the periplasm".

Other interesting and useful facts about the MalS protein can be found in [http://dx.doi.org/10.1074/jbc.272.35.22125 Spiess et al (1997)].

The SignalP program predicts that a 17 amino acid localisation signal (at the N terminal) is cleaved off before the protein reaches its mature form.

Iodine assay #1

We (Edinburgh 2011) placed BBa_K523001 under the control of the lac promoter (creating BBa_K523006) and streaked colonies on a starch agar plate. A (poorly characterised) negative control without this construct was also streaked out. The cells were incubated for 3 days.

One colony failed to grow for some reason, but the others did. We flooded the plate with iodine, which turns black in the presence of starch ([http://en.wikipedia.org/wiki/Iodine_test Wikipedia]):

Before the assay. Colony 1 failed to grow. Control at top.		Immediately after iodine flooding.		40 minutes after iodine flooding.

We made three observations:

1. The area under the negative control (top streak) turned black, while the areas under the malS streaks did not.
2. The iodine gradually evaporated, turning the plate clear again.
3. After 40 minutes, halos were seen around the two malS streaks.

We can think of two ways to explain observation 1:

• malS degraded starch, or:
• the control cells grew slower than the malS cells for some reason, and thus formed a thinner layer; iodine could pass through that layer to turn the starch underneath black, but could not pass through the thicker malS layer.

However, observation 3, the halos, seem to rule out this second explanation, and instead suggest actual diffusion of a starch-degrading enzyme (MalS) into the agar.

Iodine assay #2

The precise nature of the negative control above has been lost in the mists of time (it was JM109 E. coli with an unknown construct in pSB1C3).

We (Edinburgh 2011) repeated the iodine assay with a known control, PlacLacZ-bglX (part BBa_K523014). This part is a good control since it has both Plac-LacZ (like this part) and a periplasmic protein (like this part), and is known to actually work.

(Another control, using only Plac-LacZ, failed to grow because the source cells had been in the cold room too long.)

Control at top. Bottom two streaks are malS.		Same plate, time = 25 minutes.		Same plate, time = 70 minutes. While the iodine has faded from all the bacteria, halos are now visible around the malS streaks but not the control.

DNS assay

We (Edinburgh 2011) made cell extracts using this part and compared them to a negative control (BBa_K523000) in the following way:

Cells were sonicated and fractionated to obtain cell lysate and cell debris. 0.2% starch solution and phosphate buffered saline (PBS) were mixed with cell extract and incubated at 37 C. Every 30 minutes, a sample was taken from the reaction and 3,5-dinitrosalicylic acid (DNS) was added. The sample was heated in boiling water for 10 minutes. Enzyme activity was then halted by addition of potassium tartrate. The sample was cooled to room temperature and OD₅₇₅ was measured.

If the cell extract is capable of starch degradation, this will cause the liberated glucose to react with the DNS, producing 3-amino,5-nitrosalicylic acid and so increasing the OD₅₇₅ reading. The data are clearest for the cell lysate, but overall seem to indicate starch degradation:

Left side shows data for 2 experiments (and 2 controls) using cell lysate; right side shows data for cell debris (CD).

Mucoid phenotype

Streaks of E. coli with this part, and grown on starch agar, eventually show a mucoid phenotype so pronounced they were described as "disgusting" by a hardened microbiologist. This phenotype is only visible after several days, and was first spotted on plates that had already been subjected to iodine treatment, so we (Edinburgh 2011) checked plates that were never subjected to iodine. These too show the effect:

Starch agar. Mucoid (slimy) phenotype. All colonies are malS.		Same plate, held up to the light. Control failed to grow because it wasn't chloramphenicol resistant. Oops.

Mucoid phenotype "transmission"

We (Edinburgh 2011) wanted to check that a control strain of E. coli without this part doesn't display a mucoid phenotype on starch agar, and so E. coli with the aforementioned Plac-bglX part (BBa_K523014) was streaked out onto a starch agar plate alongside some more malS streaks.

We noticed an interesting fact: whether the control strain showed a mucoid phenotype depended on how close the cells were to the malS streaks. The part of the streak that was close to a malS streak did, while the part that was furthest away did not.

The new starch agar plate. As before, one of the controls (top) failed to grow due to an extended period in the cold room.

This seems to suggest that the MalS protein, or its products, are diffusing through the agar, and causing the nearby cells to show the same mucoid phenotype.

Growth on (minimal) starch agar

The starch agar mentioned above also had other carbon sources present. We tested the ability of K523006 to grow on minimal media but with only starch added as a carbon source. Indeed it could, while normal E. coli displayed weak or no growth:

Growth on M9 minimal media with starch.

Future experiments: Mucoid phenotype on LB agar

A control ought to be run testing whether this part displays the mucoid phenotype on normal agar. On the assumption that this phenotype is related to starch degradation, it should not.

We (TecCEM_HS 2015) ran this experiment to see the phenotype difference between the bacteria that have BBa_K523006 in starch agar and in normal LB agar (no starch). There wasn't any mucoid phenotype to be seen on LB agar in comparison to starch agar, which showed the mucoid phenotype. We can observe that the mucoid phenotype that is shown by E.coli is in fact related to the ability of this part to degrade starch.

Starch agar after Iodine assay. Mucoid phenotype can be seen.		LB (Cam+) agar, the phenotype is not mucoid. All colonies contain BBa_K523006.

Discussion

There is clear evidence that malS, when expressed from a high copy number plasmid, is capable of at least mild starch degradation.

The mucoid phenotype was unexpected. It is possible that starch degradation has led to a high supply of glucose, leading to extra exopolysaccharide being produced. This might also explain the "transmission" of the phenotype to nearby cells.

Sequence and Features