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Journal of Bacteriology, September 2005, p. 6379-6385, Vol. 187, No. 18
0021-9193/05/$08.00+0     doi:10.1128/JB.187.18.6379-6385.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.

Partial Restoration of Antibacterial Activity of the Protein Encoded by a Cryptic Open Reading Frame (cyt1Ca) from Bacillus thuringiensis subsp. israelensis by Site-Directed Mutagenesis

Mark Itsko,^* Robert Manasherob, and Arieh Zaritsky

Department of Life Sciences, Ben-Gurion University of the Negev, P.O. Box 653, Be'er-Sheva 84105, Israel

Received 13 February 2005/ Accepted 9 May 2005

Top Abstract Introduction Materials and Methods Results Discussion References

 
Insecticidal crystal proteins of Bacillus thuringiensis belong to two unrelated toxin families: receptor-specific Cry toxins against insects and Cyt toxins that lyse a broad range of cells, including bacteria, via direct binding to phospholipids. A new cyt-like open reading frame (cyt1Ca) encoding a 60-kDa protein, has recently been discovered (C. Berry et al., Appl. Environ. Microbiol. 68:5082-5095, 2002). Cyt1Ca displays the structure of a two-domain fusion protein: the N-terminal moiety resembles the full-length Cyt toxins, and the C-terminal moiety is similar to the receptor-binding domains of several ricin-like toxins, such as Mtx1. Neither the larvicidal activity of cyt1Ca expressed in Escherichia coli nor the hemolytic effect of His-tagged purified Cyt1Ca has been observed (R. Manasherob et al., unpublished). This was attributed to five amino acid differences between the sequences of its N-terminal moiety and Cyt1Aa. The 3' end of cyt1Ca was truncated (removing the ricin-binding domain of Cyt1Ca), and six single bases were appropriately changed by site-directed mutagenesis, sequentially replacing the noncharged amino acids by charged ones, according to Cyt1Aa, to form several versions. Expression of these mutated cyt1Ca versions caused loss of the colony-forming ability of the corresponding E. coli cells to different extents compared with the original gene. In some mutants this antibacterial effect was associated by significant distortion of cell morphology and in others by generation of multiple inclusion bodies spread along the cell envelope. The described deleterious effects of mutated cyt1Ca versions against E. coli may reflect an evolutionary relationship between Cyt1Aa and Cyt1Ca.

Top Abstract Introduction Materials and Methods Results Discussion References

 
Bacillus thuringiensis is a gram-positive soil bacterium that during sporulation produces large amounts of specific insect larvicidal proteins (known as -endotoxins) aggregated in parasporal bodies (6). It is widely used as a base for commercial preparations of microbial insecticides (27, 28, 34).

Insecticidal crystal proteins of different B. thuringiensis subspecies are classified into two unrelated families: receptor-specific Cry toxins that permeabilize the membrane of midgut insect cells and Cyt toxins that lyse a broad range of cells via direct binding to phospholipids (10).

Toxins of the Cyt family are particularly found in subspecies of B. thuringiensis that are toxic for Diptera (e.g., B. thuringiensis subsp. israelensis, kyushuensis, medellin, and jegatesan). These are relatively small proteins with molecular masses of around 25 to 28 kDa. Their cytolytic activities are attributed to the ability to bind phospholipids with unsaturated chains at the syn-2 position (17, 32) that predominantly compose dipteran cell membranes (14).

Seven cytolytic, mosquitocidal toxins are currently known and characterized on the biochemical level (7, 12, 13, 19, 21, 31, 42); the most investigated toxin is Cyt1Aa from B. thuringiensis subsp. israelensis. Although Cyt1Aa exhibits low toxicity by itself, it acts highly synergistically with Cry toxins (9, 20) and heterologous toxins, such as Bin from Bacillus sphaericus (38). Because Cyt1Aa plays a critical role in suppressing resistance to Cry toxins in target insects (15, 39, 40), Cyt1Aa is invaluable for improving mosquito-controlling bacterial strains (16).

General cytolytic effects of Cyt toxins against a variety of eukaryotic (33) and prokaryotic cells attract interest beyond insect pest management. Antibacterial activity of Cyt1Aa is well reported: e.g., it is bactericidal to Micrococcus luteus (43). Expression of cyt1Aa in B. thuringiensis subsp. kurstaki (41) or Escherichia coli (11, 24) causes loss of viability, accompanied in the latter by pronounced nucleoid compaction (25). The cytotoxicity of Cyt1Aa against eukaryotic cells may render it useful for cancer treatment if specificity to tumor cells is raised by, for example, linking it chemically to targeting ligands (2). Due to potential important biological role for Cyt toxins, screening for new cyt genes is on the current agenda (18).

A new cyt-like open reading frame, cyt1Ca, encoding a 60-kDa protein, has recently been discovered in B. thuringiensis subsp. israelensis (5). Its predicted product displays the structure of a two-domain fusion protein: the N-terminal part resembles the common Cyt toxins, and the C-terminal part is similar to the receptor-binding domain of ricin-B lectin type, found in several unrelated toxins, such as ricin, Clostridium botulinum neurotoxin and the mosquito-larvicidal Mtx1 toxin from B. sphaericus (5).

Discovering a potentially cytolytic protein from the Cyt family with a binding domain raises an attractive hypothesis, that it is targeted to the cell via a receptor, as Cry family toxins do. This mode of action is rather new for Cyt toxins. The Cyt-like domain of Cyt1Ca is 72% homologous to Cyt1Aa. Neither the larvicidal activity of cyt1Ca expressed in E. coli nor the hemolytic effect of His-tagged purified Cyt1Ca was found (23). This inactivity may be attributed to differences in five amino acids between its Cyt-like (N-terminal) moiety and Cyt1Aa (37) (Fig. 1): five noncharged amino acids (three Gln, a Gly, and an Ala) in the former compared to charged ones (two Lys, a Glu, and an Asp) and a Cys in the latter. In attempts to obtain a toxic variant(s) of Cyt1Ca and dissect the dual actions of Cyt1Aa, the 3' end of cyt1Ca was truncated (removing the C-terminal domain), and thoroughly chosen single bases in the remaining domain were treated appropriately by site-directed mutagenesis to change the noncharged amino acids to charged amino acids or cysteine as in Cyt1Aa.

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FIG. 1. (A) Sequence alignment of Cyt1Aa and the Cyt-like domain of Cyt1Ca with the secondary structure elements in Cyt2Aa. The amino acids important for Cyt1Aa activity (37) are shown in large type; the amino acids replaced in this study are shown in large grey type and numbered. Underlined amino acids are predicted to be on the Cyt1Aa surface (22, 26). Arrows point to Cyt1Ca truncations, according to the full-length Cyt1Aa (grey) and proteinase K activation (black). Gaps introduced to maximize alignment (dashes) are shown. (B) A schematic ribbon diagram determined by X-ray crystallography of a monomer of Cyt2Aa (22). The structure shows a three-layered /ß architecture where the -helices form the outer layer and ß-strands (marked as in reference 22) are buried within the core of the protein.

Top Abstract Introduction Materials and Methods Results Discussion References

 
Bacterial strains and plasmids. E. coli XL-Blue MRF' and plasmids used in this study are listed in Table 1.

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TABLE 1. pUHE-24S-based plasmids encoding the described products

Cultures were grown at 37°C in LB broth supplemented with 100 µg ml^–1 ampicillin to an optical density at 660 nm of 0.2 to 0.3 (2 x 10⁸ cells ml^–1) and induced by 1 mM of isopropyl-ß-D-thiogalactoside (IPTG).

PCR. Truncated versions of cyt1Ca were amplified from pBtoxis of B. thuringiensis subsp. israelensis (5) with Taq polymerase (MBI Fermentas) in a DNA thermal cycler for 30 reaction cycles, with each cycle consisting of 50 s at 94°C, 50 s at 50°C, and 50 s at 72°C.

The primers for the C-terminally truncated version of Cyt1Ca (CyCtrC) were a 39-mer, 5'-CAGTAATTTCTAGAGCACTTCTTTAATTTACGGAAGTTA-3', containing an XbaI restriction site (bold type) and a translation termination site (underlined), and a 30-mer, 5'-CCAGGGGGCGAGTCCATGGCTCAATCAGAA-3', containing an NcoI restriction site (bold type). For the N- and C-terminally truncated versions (CyCtrNC), the primers were a 42-mer, 5'-CGTGCAAGAGCCATGGTTCTACGTGTGGAAGACCCGGGATAC-3', containing an NcoI restriction site (bold type), and a 37-mer, 5'-GCCTCTTAGGTCTAGAAATTACTCATGAATCAATGGC-3', containing an XbaI restriction site (bold type) and a translation termination site (underlined).

Construction of plasmids. The blunt-end PCR products (659- and 774-bp fragments for cyCtrNC and cyCtrC, respectively) were digested with NcoI/XbaI and inserted into the same sites of pUHE-24S to get pUH-cyCtrC and pUH-cyCtrNC, respectively.

Site-directed mutagenesis. The site-directed mutagenesis method used was based on Stratagene's QuikChange site-directed mutagenesis kit. The recombinant plasmids pUH-cyCtrC and pUH-cyCtrNC were used as templates for the single and double amino acid changes Q148K Q159E, G235D, A185C, and Q220K, together with the appropriate primers shown in Table 2. For multiple amino acid changes at distant places, templates of previously mutated versions were used. For each mutant, the recombinant plasmid was confirmed by digestion with the restriction endonuclease (Table 2), and the DNA sequence was verified by an automated DNA sequencer.

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TABLE 2. Sequences of the primers used to construct the site-directed mutants

Viable cell counts. Cell viability was determined by measuring the ability to form colonies on LB plates (with 100 µg ampicillin ml^–1) following appropriate dilutions and with IPTG when indicated. The number of colonies was counted after 24 h of incubation at 37°C.

Microscopy. Aliquots of growing cultures were fixed (0.25% formaldehyde), immobilized on agarose slides as described previously (35), and cells were visualized by phase-contrast microscopy (Zeiss Axioplan 2) and photographed using IPLAB 3.1a (Signal Analytics).

Mosquito larvicidal assay. Cells were harvested by centrifugation after 4 h of induction and resuspended in distilled water. Samples were added to 20 early third-instar Aedes aegypti larvae in disposable cups with 100 ml sterile tap water, and mortality was determined after 24 h at 28°C (4). Presumed synergy between mutated versions of Cyt1Ca and Cry4Aa was tested using mixtures of two clones containing 4:1 ratios (by cell number) of clones expressing different cyt1Ca versions and a clone expressing cry4Aa, respectively.

Top Abstract Introduction Materials and Methods Results Discussion References

 
Rationale for the selection of amino acids to be replaced in Cyt1Ca. Cyt1Aa has 13 positively and negatively charged amino acids that are critical for its activity; changing either of them to alanine affects its toxicity considerably (37). Aligning the sequence of the Cyt-like domain of Cyt1Ca with that of Cyt1Aa reveals that some of these 13 have changed to noncharged amino acids: K154 in Cyt1Aa changed to Q149 in Cyt1Ca; E164 in Cyt1Aa changed to Q159 in Cyt1Ca; K225 changed to Q220, and D240 changed to G235 (Fig. 1). Moreover, the only cysteine in the activated form of Cyt1Aa (C190) that is also important for its activity (8) is changed to alanine in Cyt1Ca (A185). The inactivity of the latter (23) is attributed to these five changes and hence we decided to sequentially change them back to those in the original Cyt1Aa. The replacements were implemented on two different truncated versions of Cyt1Ca: one (cyCtrC), at N244 (as in the full-length Cyt1Aa), and the second (cyCtrNC), at both ends, at I21 and E228 (as in proteinase K-activated fragment of Cyt1Aa). In addition, N6 and N7 in cyCtrNC were replaced by E6 and D7, respectively (as in Cyt1Aa).

Deleterious effects to E. coli of the mutated Cyt1Ca (Fig. 2). Expression of the nonmutated cyCtrC delayed cell division for an hour starting 30 min after induction. Its doubly mutated Q149K Q159E version (cyCtrC12) delayed cell division for 210 min. The additional mutations G235D and A185C (in cyCtrC3 and cyCtrC4) emphasized this effect, leading to three- and sixfold drops in the colony-forming ability 3 h after induction, respectively. Very slow recoveries were observed afterwards. The last sequential mutation Q220K (in cyCtrC5) abolished the killing effect of cyCtrC3 and cyCtrC4 while division arrest remained.

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FIG. 2. Viable cell counts of E. coli strains harboring plasmids cloned with different cyt1Ca versions without (open symbols) or with (closed symbols) induction by IPTG: , cyCtrC; •, cyCtrC12; , cyCtrC3; , cyCtrC4; , cyCtrC5.

The difference in the viability of cells expressing different mutated versions of the truncated cyt1Ca was emphasized upon indefinite induction, when cells were spread out on IPTG-containing plates (Table 3). Here, viabilities of cells with both truncated versions were monitored and compared with that of the clone expressing cyt1Aa. Surprisingly, the mutant cyCtrNC4 (with four substitutions, i.e., Q149K Q159E G235D A185C) was 10-fold less viable than its counterpart in the C-terminally truncated version cyCtrC4 and only 5-fold more viable than the clone (pRM4-C) expressing cyt1Aa (24).

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TABLE 3. Viabilities on IPTG-containing LB plates

Morphologies of inclusion bodies in the clones expressing cyCtrC. The nonmutated version formed a large inclusion body situated at the E. coli cell pole (Fig. 3A to D), while all four mutated versions generated multiple inclusion bodies spread along the cell envelope (e.g., Fig. 3E to H). On the other hand, expressing cyCtrNC (Cyt1Ca truncated at both termini according to the proteinase K activation pattern) and its mutated versions did not bring about the formation of inclusion bodies (Fig. 4).

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FIG. 3. Morphology of inclusion bodies formed by expressed cyt1Ca versions in E. coli. Cells harboring pUH-cyCtrC (A-D) and pUH-cyCtrC4 (E-H), uninduced (A, E) and after 2 h (B, F), 4 h (C, G), and 20 h (D, H) of induction by IPTG. Bars, 5 µm.

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FIG. 4. Cell morphology of E. coli cells expressing different versions of cyt1Ca 3 h after induction by IPTG: cyCtrNC (A) and cyCtrNC12 (B). Bars, 5 µm.

Cell morphology (Fig. 4). Expressing cyCtrNC12, cyCtrNC6, and cyCtrNC4 (Table 1) caused pronounced distortions of cell morphology. Three hours after induction by IPTG, about 30% of the cells became elongated, bent, and bulged (Fig. 4), while expressing the mutated versions of cyCtrC caused cell elongation only (Fig. 3). This distortion accompanied inhibition of cell divisions upon expression of cyCtrNC12 and cyCtrNC6 (not shown) and viability loss upon expression of cyCtrNC4 (Table 3).

Bioassay of the mutated proteins. None of the E. coli clones expressing cyt1Ca or any of its mutated versions displayed toxicity against larvae of A. aegypti (not shown) or synergistic activity with a strain expressing cry4Aa (Fig. 5).

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FIG. 5. Mortality of third-instar Aedes aegypti larvae upon feeding the larvae with the mixture containing the clone pHE4-A mixed with the following clones: pUHE-24S (A), pUH-cyCtrC (B), pUH-cyCtrC4 (C), and pRM4-C (D). Mixtures were prepared as described in Materials and Methods.

Top Abstract Introduction Materials and Methods Results Discussion References

 
The recently discovered open reading frame in pBt054 (5) encodes a protein, Cyt1Ca, which surprisingly is not toxic to mosquito larvae or to E. coli (23) despite the high homology of its N-terminal domain to the full-length Cyt1Aa (Fig. 1). No Cyt1Ca has yet been identified in B. thuringiensis subsp. israelensis. The question thus arises of its possible function in the bacterial life cycle, toxicity, or evolution. To start deciphering this enigma, five versions of cyCtrC (encoding the N-terminal 244 amino acids that resemble Cyt1Aa) containing combinations of sequential mutations were constructed (Tables 1 and 2; Fig. 1). Expressing them in E. coli caused cumulative deleterious effects. Delay or inhibition of cell division in all mutants and loss of viability in some of the mutants (Fig. 2; Table 3) were accompanied by the appearance of multiple inclusion bodies positioned in proximity to the cell envelope (Fig. 3). These results point to a possible interaction of the changed Cyt1Ca with the inner membrane of E. coli that may interfere with its division machinery and damage the membrane causing cell lysis as Cyt1Aa does (25).

Initial contact of Cyt1Aa with membranes involves electrostatic interactions of the charged amino acids, situated on its surface, with the lipid head groups (26). The toxin binds in vitro specifically to zwitterionic phospholipids, such as phosphatidylcholine and phosphatidylethanolamine (32). The latter is the major phospholipid in the E. coli inner membrane (29) and has been proposed to be localized in segregated domains (36). The interaction of Cyt1Aa with these domains may be responsible for its toxicity against E. coli (25). Particular amino acids have been assigned as possible candidates for this interaction (26), among which are K154, E164, and D240 (Fig. 1). Thus, one of the factors causing the absence of Cyt1Ca activity may be the noncharged nature of the amino acids corresponding to the above (Q149, Q159, and G235). Changing them back as in Cyt1Aa indeed partially restored activity of C-terminally truncated Cyt1Ca (Fig. 2 and Table 3).

Not all the chosen substitutions in Cyt1Ca enhance the antibacterial effect. For example, the Q220K substitution in CyCtrC12 (forming CyCtrC6) or CyCtrC4 (CyCtrC5) decreased their killing effects against E. coli cells (Table 3). Q220 in Cyt1Ca is homologous to K225 in Cyt1Aa, but the latter is situated in the inner core of Cyt1Aa rather than on its surface (22) (Fig. 1). It therefore seems not to be involved in initial binding to the lipid head groups via electrostatic interactions but in membrane penetration afterwards (22). The effect of the Q220K substitution in Cyt1Ca may thus be more complicated than substitutions of the others. Stronger suppression by Q220K of the quadruple Q149K Q159E G235D A185C than of the double substitution Q149K Q159E in Cyt1Ca may be explained by the lower affinity to the membrane of the amino acid combination C185 K220 than of the combination C185 Q220. This interpretation is supported by the fact that homologous amino acids K225 and C190 (in Cyt1Aa) to Q220 and A185 (in Cyt1Ca), respectively, are contiguous when mapped into the three-dimensional structure of Cyt2Aa, the only Cyt-like protein deciphered (22). However, the analogous suppression of CyCtrC12 by Q220K (Table 3) apparently contradicts this conclusion. It seems as though the original Q220 is more effective against E. coli than K220 at a given amino acid context in Cyt1Ca.

Full toxicity of Cyt1Aa in the midgut of the target organism, mosquito larvae, needs a two-end proteolytic activation (1). Similar processing in vitro has been achieved by proteinase K (1), which is why CyCtrNC and its mutant derivatives were constructed (Tables 1 and 2). The deleterious effects of some of these derivatives to E. coli were greater than that of the mutated protein truncated just at N244: the division inhibition of E. coli expressing these versions of mutated cyt1Ca was accompanied by pronounced distortion of cell morphology (Fig. 4) not occurring when any of the mutated versions of cyCtrC were expressed. Moreover, viability of cells expressing cyCtrNC4 was five times lower than those expressing cyCtrC4 (Table 3). The difference in activities damaging E. coli cells between C-terminally truncated and doubly truncated Cyt1Ca can be explained by an aggregation-prone nature of the former compared to the latter (Fig. 3): generation of inclusion bodies may prevent the aggregated protein from efficient interaction with the membrane.

The relative importance of different charged (37), hydrophobic (3) amino acids for Cyt1Aa activity and tryptophans for Cyt2Aa2 activity (30) has been studied systematically by site-directed mutagenesis. Knocking down activities of these proteins by amino acid substitutions revealed rather easily the significance of the replaced amino acids in Cyt function. An attempt was undertaken here to solve the problem the other way around, by restoring the presumably lost function of Cyt1Ca in a learned way. The described deleterious effects of mutated cyt1Ca versions on E. coli may reflect an evolutionary relationship between Cyt1Aa and Cyt1Ca. Expression of cyt1Aa in E. coli resulted in abrupt arrest in biomass growth and nucleoid compaction, the mechanism of which probably involves disturbing all or most of the membrane functions (25). These effects were not observed in E. coli (not shown) when it expressed even the most bactericidal versions of mutated cyt1Ca: cyCtrC4 and cyCtrNC4 (Table 3). Expression of these genes exerted lethality on E. coli in a much more moderate and slower mode probably because it affects a limited number of membrane functions, such as division machinery and shape determination. Moreover, the affinities of the mutated versions of Cyt1Ca to the bacterial membrane that resulted in the above effects is not adequate to its larvicidity against A. aegypti (Fig. 5). The original question posed, what does the so-called cyt1Ca open reading frame do in pBtoxis, is thus not resolved yet, and further genetic and biochemical analyses are required. However, the approach to acquire bactericidal abilities to totally inactivate Cyt1Ca is very promising in clarifying the yet enigmatic general bactericidal effect of Cyt1Aa.

 
This investigation was partially supported by a grant (97-00081) from the United States-Israel Binational Science Foundation (BSF), Jerusalem, Israel.

Thanks are due to Eitan Ben-Dov and Itzhak Fishov for fruitful discussions.

 
* Corresponding author. Mailing address: Department of Life Sciences, Ben-Gurion University of the Negev, P.O. Box 653, Be'er-Sheva 84105, Israel. Phone: 972-8-6461 712. Fax: 972-8-6278 951. E-mail: ariehz{at}bgu.ac.il.

Present address: Department of Genetics, Stanford University School of Medicine, Stanford, CA 94305-5120.

Top Abstract Introduction Materials and Methods Results Discussion References

 

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Journal of Bacteriology, September 2005, p. 6379-6385, Vol. 187, No. 18
0021-9193/05/$08.00+0     doi:10.1128/JB.187.18.6379-6385.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.

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