Key residues of Bacillus thuringiensis Cry2Ab for oligomerization and pore-formation activity

As a pore-forming toxin, activation, oligomerization and pore-formation were both required for the mode of action of Cry toxins. Previous results revealed that the helices α4–α5 of Domain I were involved in the oligomerization of Cry2Ab, however, the key residues for Cry2Ab aggregation remained ambiguous. In present studies, we built 20 Cry2Ab alanine mutants site-directed in the helices α4–α5 of Domain I and demonstrated that mutants N151A, T152A, F157A, L183A, L185A and I188A could reduce the assembly of the 250 kDa oligomers, suggesting that these mutation residues might be essential for Cry2Ab oligomerization. As expected, all of these variants showed lower insecticidal activity against P. xylostella. Furthermore, we found that the pore-forming activities of these mutants also decreased when compared to wild-type Cry2Ab. Taken together, our data identified key residues for Cry2Ab oligomerization and emphasized that oligomerization was closely related to the insecticidal activity and pore-forming activity of Cry2Ab. Supplementary Information The online version contains supplementary material available at 10.1186/s13568-021-01270-0.


Introduction
Cry toxin, an insecticidal crystal toxin derived from Bacillus thuringiensis (Bt), is widely applied as a bioinsecticides to control agricultural pests all over the world (Bravo et al. 2011;Schnepf et al. 1998). In general, Cry toxins are produced in an inactive form called protoxin and proteolytic activated by target insect midgut protease. Activated Cry toxins interacted with the midgut receptors in target insects, self-aggregated to form pre-pore oligomeric structures and inserted into the cell membrane to form pores, resulting in the destruction of the midgut epithelium and the death of insects (Pardo-López et al. 2013;Bravo et al. 2007;Vachon et al. 2012).
At present, most researches have been devoted into "interaction of Cry toxins with midgut receptors" which is an essential step for the insecticidal mechanism of Cry toxins (Pigott and Ellar 2007;Bravo et al. 2013). As a result, a number of insect midgut proteins such as cadherin, aminopeptidase-N (APN), alkaline phosphatase (ALP) and ATP-binding cassette transporter subfamily C member 2 (ABCC2) have been proposed as functional receptors and mediated the insecticidal activities of Cry toxins (Pigott and Ellar 2007;Zhou et al. 2017;Park et al. 2009;Guo et al. 2015;Chen et al. 2017). It was suggested that the mutation or down-regulation of Cry receptor genes were tightly linked with high level of Cry resistance in diverse insects (Ferré and Van Rie 2002;Baxter et al. 2011). It was also reported that the improper processing of Cry toxins was associated with Cry resistance in lepidopteran insects Xia et al. 2016). Those studies made a closer look on the mechanism of Cry toxins and provided new strategies for agricultural pest control.
As a pore-forming toxin, Cry toxins kill insects by forming pore on their midgut cells. Assembly of prepore oligomers was required for pore-forming processing of Cry toxins (Jiménez-Juárez et al. 2013;Vachon et al. 2002). Domain I, comprised by seven-helix bundle, was widely reported involving in the assembly of pre-pore structure and membrane channel formation (Pardo-López et al. 2013;Vachon et al. 2012). It was proposed that a binding step of cadherin receptors and proteolytic Open Access *Correspondence: zyjingfz@163.com 1 Agricultural Bio-Resources Research Institute, Fujian Academy of Agricultural Sciences, Fuzhou 350003, China Full list of author information is available at the end of the article removal of helix α-1 were necessary for oligomerization of Cry1A toxin (Soberón et al. 2007). Helix α-3 was found to participate in toxin oligomerization as the mutation on this region affected oligomerization, as well as toxicity of Cry toxin (Vachon et al. 2002;Muñoz-Garay et al. 2009). Recently, Pacheco et al. reported that an intramolecular salt bridge in helix α-3 was essential for the stability and oligomerization of Cry4Ba toxins (Pacheco et al. 2017). The helices α-4 and α-5 had been wildly reported as a pore-forming region, as they were the only helices capable of adopting a transmembrane orientation (Girard et al. 2008;Torres et al. 2008). An umbrella model was further put forward in which the helices α-4 and α-5 inserted into the membrane to form pores while other αhelices covered the surface of membrane (Pardo-López et al. 2013).
Our previous study suggested that the exposure of helices α4-α5 was required for oligomerization and insecticidal activity of Cry2Ab (Xu et al. 2018). However, the key residues involved in the oligomerization activity of Cry2Ab were still unknown. In the present study, we sought to determine the key residues of Cry2Ab for oligomerization activity by constructing 20 alanine mutants site directed on helices α4-α5. It revealed that residues N151, T152, F157, L183, L185 and I188 are involved in Cry2Ab oligomerization. The Cry2Ab mutants with lower activities of oligomerization not only reduced the insecticidal activities against Plutella xylostella, but also weakened the pore-forming activities on liposome. Our data firstly identified key residues for Cry2Ab oligomerization and highlighted that oligomerization was linked with the insecticidal activity and pore-forming activity of Cry2Ab.

Insects
A laboratory population of P. xylostella larvae was purchased from Henan Jiyuan Baiyun Industry Co., Ltd, China. P. xylostella larvae were fed with an artificial diet and maintained under environmental conditions of 27 ± 2 °C, 70% of humidity, and photoperiod of 14:10 h (light/dark).

Expression of Cry2Ab variants
The production and purification of wild-type and mutant Cry2Ab toxins were performed as previously described (Pan et al. 2014). E. coli BL21 (DE3) cells harboring pET30a-cry2Ab were grown in LB medium containing 35 µg/mL kanamycin. The expression of wild-type and mutants Cry2Ab toxins were induced overnight at 25 °C with 0.5 mM isopropyl-B-d-thiogalactopyranoside (IPTG) after OD 600 nm reached 0.4-0.6. Cells were pelleted at 6000 g under 4 °C and resuspended with Tris-HCl buffer (25 mM Tris-HCl, 300 mM NaCl, 25 mM imidazole, pH 7.0) and then lysed by ultrasonication. The soluble Cry2Ab toxins were purified by a Ni-IDA Prepacked Column (Sangon, China) according to the instruction manual. Purified Cry2Ab were detected by 10% SDS-PAGE and western blotting using an anti-Cry2Ab antibody. Protein concentration of Cry2Ab toxins were determined using a BCA Protein Assay Kit (Beyotime, China).

Oligomerization assay
Cry2Ab protoxin was incubated with P. xylostella midgut juice (PxMJ) with a mass ratio of 20:1 (m: m) at 30 °C for 60 min and exchanged into sodium carbonate buffer (50 mM, pH 9.5) using a PD-10 desalting column. The brush border membrane vesicles from P. xylostella midguts were prepared as Wolfersberger et al. reported (1987). For oligomeric formation assays, 20 µg of Cry2Ab activated-toxin was incubated at 30 °C overnight in the present of PxBBMV (10 µg). The oligomeric formation of Cry2Ab was detected by 8% SDS-PAGE with Coomassie staining (Xu et al. 2018). The ratio of oligomerization percentage was calculated by Image J software to evaluate the percentage of oligomer (oligomer/monomer × 100%).

Bioassay
Bioassays of wild-type and mutants Cry2Ab toxins against second instar larvae of P. xylostella were estimated according to Pan et al. (2014). A 2 mL artificial diet was added to 6-well polystyrene plates (Sangon, China) and air-dried. Five or six concentrations of Cry2Ab toxins from 0.032 to 20 µg/cm 2 were set up. Insects tested with sodium carbonate buffer (50 mM, pH 9.5) were served as the negative control. Thirty second instar larvae of P. xylostella were used for each concentration assay and three independent replicates were performed.
Observations were recorded at 48 h, and the median lethal concentration (LC 50 ) value was analyzed by SPSS 17.0 (Statistical Product and Service Solutions) using PROBIT analysis (Finney 1971). The relative potency (%) had been normalized to the LC 50 value of wild-type Cry2Ab.

Liposome leakage assay
Liposome preparation was performed as described by Ding et al. (2016). Phosphatidylcholine, phosphatidylethanolamine and cholesterol were dissolved in chloroform and mixed in a 4:4:2 proportion (molar mass). The mixed lipids were put in a glass vial and evaporated under a stream of nitrogen to form lipid film. The lipid film was then shaking with SUV-1 buffer (20 mM HEPES, 50 mM NaCl, 3 mM calcein, pH 7.5) at room temperature for 2 h. Liposomes were generated by extrusion of the hydrated lipids through a 100-nm polycarbonate filter (Whatman) 35 times using a Mini-Extruder device (Avanti Polar Lipids Inc). Calcein, outside the liposome, were removed by exchanging the liposome into SUV-2 buffer (20 mM HEPES, 50 mM NaCl, pH 7.5) using a Sephadex G-50 column. Liposomes were stored at 4 °C and used within 48 h.
For liposome leakage assay, the liposome encapsulated calcein was diluted to 200 µM in SUV-2 buffer supplemented with 3 µM MnCl 2 . The released calcein could be quenched by MnCl 2 in the solution. The excitation and emission wavelengths were set as 490 nm and 520 nm, respectively, to examine the fluorescence of calcein. 480 µL of liposome was added to the cuvette and the emission fluorescence was readed as F t0 . 20 µL of activated-Cry2Ab (10 µg) was then added to and the emission fluorescence was continuously recorded as Ft at 10 s intervals. After 10 min, 20 µL of 10% Triton X-100 was added to achieve complete release of calcein and the fluorescence records were defined as F t100 . The percentage of liposome leakage at each time point is defined as:

Production and identification of Cry2Ab mutants
The expression of Cry2Ab variants were performed under the induction of 0.5mM IPTG. SDS-PAGE revealed that all Cry2Ab mutants could be induced to express with a molecular weight of 65 kDa ( Fig. 2A). Those Cry2Ab mutants further purified by a Ni-IDA prepacked column (Fig. 2B) and could be detected by an anti-Cry2Ab antibody (Fig. 2C). Furthermore, proteolysis assay indicated that all Cry2Ab variants could be processed into 50 kDa activated-toxins by PxMJ, which were similar to wild-type Cry2Ab (Fig. 2D). These results revealed that mutations in the helices α4-α5 did not cause a major structural disturbance in Cry2Ab.
To further assess the oligomers formation of Cry2Ab, we employed Image J software to evaluate the percentage of Cry2Ab oligomer (oligomer/monomer × 100%). As shown in Fig. 3B, the proportion of oligomer and monomer in normal oligomerization group was about Fig. 2 Expression, purification and identification of Cry2Ab mutants. A Induced expression of Cry2Ab variants. B The purity of Cry2Ab mutants detected by SDS-PAGE followed by Coomassie blue staining. C Identification of Cry2Ab mutants using an anti-Cry2Ab antibody. D The proteolytic activation of Cry2Ab mutants by PxMJ 80-110%, which was similar to wild-type Cry2Ab (the percentage was about 95%). However, this value went down to 40-60% in reduced oligomerization group and were less than 20% in non-aggregation group. These results suggested that residues N151, T152, F157, L183, L185, I188 might serve as key residues for Cry2Ab oligomerization.

Oligomerization is associated with insecticidal activity of Cry2Ab
We then evaluated the insecticidal activities of non-oligomerization Cry2Ab mutants (N151A, T152A, F157A, L183A, L185A and I188A) against second instar larvae of P. xylostella, with wild-type Cry2Ab, V150A and S186A (two Cry2Ab mutants in normal oligomerization group) as positive control. As shown in Table 1, the LC 50 values of V150A and S186A was 1.978 and 1.432 µg/cm 2 , respectively, which were close to that of wild-type Cry2Ab (1.458 µg/cm 2 ). However, the LC 50 values of N151A, T152A, F157A, L183A, L185A and I188A were 5.097, 4.232, 3.234, 3.083, 3.579 and 3.545 µg/cm 2 , respectively, all of which were higher than that of wild-type Cry2Ab. These results indicated that oligomerization was associated with the insecticidal activity of Cry2Ab.

Oligomerization is linked with pore-forming activity of Cry2Ab
The pore-forming activities of non-oligomerization Cry2Ab mutants (N151A, T152A, F157A, L183A, L185A and I188A) were further assessed by time course of liposome leakage assay. As shown in Fig. 4, wild-type Cry2Ab activated-toxin could make pore on liposome and led to high leakage of calcein into solution, which was the same with V150A and S186A variants. The maximum calcein release percentage caused by wild-type Cry2Ab, V150A and S186A activated-toxin were 60.95%, 55.87%, and 58.73%, respectively. However, the leakage of calcein caused by N151A, T152A, F157A, L183A, L185A and I188A activated-toxins were only 24.33%, 20.72%, 35.98%, 32.36%, 37.53 and 32.53%, all of which were lower than wild-type Cry2Ab. These data demonstrated that nonoligomerization mutants could weaken the pore-forming activities on liposome. Taken together, our data indicated that oligomerization was linked with the pore-forming activity of Cry2Ab.

Discussion
The helices α-4 and α-5 of Cry1A had been wildly reported as a pore-forming region (Girard et al. 2008;Torres et al. 2008). In other Cry toxin, helices α-4 and α-5 also reported in the oligomerization activity. Kanintronkul et al. reported that N166 and Y170 in helices α4-α5 was involved in the aggregation of Cry4B (Kanintronkul et al. 2003). Pornwiroon et al. reported that Y202 in helices α4 was responded to the oligomerization activity of Cry4A (Pornwiroon et al. 2004). In our previous study also suggested that helices α4-α5 participate in Cry2Ab self-aggregation (Xu et al. 2018). In this study, we further constructed 20 alanine mutants site directed on helices α4-α5 and showed that residues Fig. 4 Liposome leakage assay detected pore-forming activity of Cry2Ab mutants Pan et al. AMB Expr (2021) 11:112 N151, T152, F157, L183, L185 and I188 may be key residues for Cry2Ab oligomerization and insecticidal activity.
The pore-formation of Cry toxins on the membrane was one of the less characterized steps and was indispensable to fully understand the mechanism action of Cry toxins (Muñoz-Garay et al. 2006). Zavala et al. demonstrated that only Domain I inserted into the liposome while Domain II and III remained in the surface of membrane (Zavala et al. 2011). This result was consistence with the umbrella model of toxin insertion. It also revealed that residues V171 and T122 involved in the insertion of Cry1A toxin into members by fluorescent studies. Angsuthanasombat et al. revealed that residue Arg-136 participated in the membrane channel formation of Cry4Ba (Angsuthanasombat et al. 2001). It was also reported that residue N183 located in the middle of helix α-5 was crucial for the insecticidal activity and pore-forming activity of Cry4Ba (Likitvivatanavong et al. 2006). Similarly, our data showed that mutations on helice α-4 and α-5 (N151A, T152A, F157A, L183A, L185A and I188A) also blocked the pore-formation of Cry2Ab on liposome.
It was worth mentioning that Cry2Ab mutants which failed to assemble 250 kDa oligomers, not only disrupted the insecticidal activity against P. xylostella, but also lost pore-forming activity of liposome. The results suggested that oligomerization and pore-formation was closely related in Cry2Ab. This mode of action was quite different from that of Cry1A toxin. For example, helices α-3 and α-6 of Cry1A was reported involved in oligomerization while helices α-4 and α-5 participated in poreformation (Jiménez-Juárez et al. 2013;Lin et al. 2014). Furthermore, in Cry1A toxin, it was reported that toxins oligomerization required a binding step to cadherin, which promoted to cleavage of helix α-1 (Soberón et al. 2007). However, our previous data revealed that Cry2Ab could oligomerize in vitro after proteolysis by PxMJ in the absence of the cadherin (Xu et al. 2018). This diversity suggested that the mode of action of Cry2Ab might different from Cry1A toxin in some details and more researches were needed to clarify the elaborate difference. In conclusion, our study comprehensively identified key residues for Cry2Ab for the first time and demonstrated that non-oligomerization mutants affected the insecticidal activity as well as the pore-forming activity of Cry2Ab. It highlighted that oligomerization was closely related to insecticidal activity and pore-forming activity of Cry2Ab, which could make a closer look on the mode of action of Cry2Ab toxins. Further studies will focus on the saturated mutation of these key residues to construct Cry2Ab variants with enhanced oligomerization activities as well as higher insecticidal performance.