In this paper, an asymmetric image encryption algorithm based on DNA coding and hyperchaotic system is designed. Unlike other image encryption schemes, for example, sharing of same private keys between sender and receiver, and fixed rules with simple operation, three stages are studied as follows to deal with these problems. Firstly, to eliminate the possible risk of key transmission and management, the initial values of the hyperchaotic system are generated for ahead by the RSA (Rivest-Shamir-Adleman) algorithm and the plain image, in which the sum of odd rows, even rows, odd columns, and even columns are computed respectively to extra the plain message from the plain image as input of RSA algorithm. Then, a mathematical map is established to transform all of them into initial values of the hyperchaotic system. Secondly, the pixel level permutation is performed to confuse the image according to the chaotic sequences generated. Finally, to solve the problem of fixed rules with simple operations in current DNA based image encryption algorithms, dynamical DNA encryption is designed to diffuse the permuted image. The process of DNA encryption includes DNA coding, DNA operation and DNA decoding. In particular, DNA rules are selected according to chaotic sequences dynamically, rather than fixed rules with simple operation. Theoretical analysis and numerical simulations show that the proposed algorithm is secure and reliable for image encryption.
Citation: Min Liu, Guodong Ye. A new DNA coding and hyperchaotic system based asymmetric image encryption algorithm[J]. Mathematical Biosciences and Engineering, 2021, 18(4): 3887-3906. doi: 10.3934/mbe.2021194
[1] | Vakhtang V. Dzhavakhiya, Elena V. Glagoleva, Veronika V. Savelyeva, Natalia V. Statsyuk, Maksim I. Kartashov, Tatiana M. Voinova, Alla V. Sergeeva . New bacitracin-resistant nisin-producing strain of Lactococcus lactis and its physiological characterization. AIMS Microbiology, 2018, 4(4): 608-621. doi: 10.3934/microbiol.2018.4.608 |
[2] | John Samelis, Athanasia Kakouri . Hurdle factors minimizing growth of Listeria monocytogenes while counteracting in situ antilisterial effects of a novel nisin A-producing Lactococcus lactis subsp. cremoris costarter in thermized cheese milks. AIMS Microbiology, 2018, 4(1): 19-41. doi: 10.3934/microbiol.2018.1.19 |
[3] | Natalia Y. Kovalskaya, Eleanor E. Herndon, Juli A. Foster-Frey, David M. Donovan, Rosemarie W. Hammond . Antimicrobial activity of bacteriophage derived triple fusion protein against Staphylococcus aureus. AIMS Microbiology, 2019, 5(2): 158-175. doi: 10.3934/microbiol.2019.2.158 |
[4] | Prateebha Ramroop, Hudaa Neetoo . Antilisterial activity of Cymbopogon citratus on crabsticks. AIMS Microbiology, 2018, 4(1): 67-84. doi: 10.3934/microbiol.2018.1.67 |
[5] | Joseph O. Falkinham . Mycobacterium avium complex: Adherence as a way of life. AIMS Microbiology, 2018, 4(3): 428-438. doi: 10.3934/microbiol.2018.3.428 |
[6] | Farzad Rahmati . Characterization of Lactobacillus, Bacillus and Saccharomyces isolated from Iranian traditional dairy products for potential sources of starter cultures. AIMS Microbiology, 2017, 3(4): 815-825. doi: 10.3934/microbiol.2017.4.815 |
[7] | Yusuke Morita, Mai Okumura, Issay Narumi, Hiromi Nishida . Sensitivity of Deinococcus grandis rodZ deletion mutant to calcium ions results in enhanced spheroplast size. AIMS Microbiology, 2019, 5(2): 176-185. doi: 10.3934/microbiol.2019.2.176 |
[8] | Alexandra Díez-Méndez, Raul Rivas . Improvement of saffron production using Curtobacterium herbarum as a bioinoculant under greenhouse conditions. AIMS Microbiology, 2017, 3(3): 354-364. doi: 10.3934/microbiol.2017.3.354 |
[9] | Stephen H. Kasper, Ryan Hart, Magnus Bergkvist, Rabi A. Musah, Nathaniel C. Cady . Zein nanocapsules as a tool for surface passivation, drug delivery and biofilm prevention. AIMS Microbiology, 2016, 2(4): 422-433. doi: 10.3934/microbiol.2016.4.422 |
[10] | Yunfeng Xu, Attila Nagy, Gary R. Bauchan, Xiaodong Xia, Xiangwu Nou . Enhanced biofilm formation in dual-species culture of Listeria monocytogenes and Ralstonia insidiosa. AIMS Microbiology, 2017, 3(4): 774-783. doi: 10.3934/microbiol.2017.4.774 |
In this paper, an asymmetric image encryption algorithm based on DNA coding and hyperchaotic system is designed. Unlike other image encryption schemes, for example, sharing of same private keys between sender and receiver, and fixed rules with simple operation, three stages are studied as follows to deal with these problems. Firstly, to eliminate the possible risk of key transmission and management, the initial values of the hyperchaotic system are generated for ahead by the RSA (Rivest-Shamir-Adleman) algorithm and the plain image, in which the sum of odd rows, even rows, odd columns, and even columns are computed respectively to extra the plain message from the plain image as input of RSA algorithm. Then, a mathematical map is established to transform all of them into initial values of the hyperchaotic system. Secondly, the pixel level permutation is performed to confuse the image according to the chaotic sequences generated. Finally, to solve the problem of fixed rules with simple operations in current DNA based image encryption algorithms, dynamical DNA encryption is designed to diffuse the permuted image. The process of DNA encryption includes DNA coding, DNA operation and DNA decoding. In particular, DNA rules are selected according to chaotic sequences dynamically, rather than fixed rules with simple operation. Theoretical analysis and numerical simulations show that the proposed algorithm is secure and reliable for image encryption.
Alicyclobacillus acidoterrestris is a thermoacidophilic, non-pathogenic, rod-shaped, spore-forming bacterium. It has the ability to grow in a wide temperature (25–60 ℃) and pH (2.5–6.0) ranges [1]. ω-alicyclic fatty acids are the major lipid components and provide its resistance to acidic conditions and high temperatures [2]. After fruit juice pasteurization, its spores can germinate into vegetative cells leading to spoilage [3]. Spoilage is difficult to detect visually [4] and has been detected in various pasteurized juice samples such as apple, tomato, white grape, grapefruit, orange, and pineapple juices but not in red grape juices and Cupuaçu [1].
The use of natural antimicrobials in foods inhibits the growth of many microorganisms without health risks to consumers [5]. In the food industry, it is important to determine the effects of non-thermal technologies on microbial inactivation and the growth parameters of the survivors such as the lag phase (λ) and the maximum specific growth rate (μ) [6]. Nisin is a heat stable bacteriocin produced by Lactococcus lactis sub sp. lactis. It shows antibacterial activity against Gram-positive bacteria and spore formers such as Bacillus and Clostridium spp. This antibacterial agent is essentially non-toxic to humans and degraded without causing any damage to the intestinal tract. In the United States, it was approved by the Food and Drug Administration (FDA) and allowed to be used in processed cheeses [7]. In the food industry, it has been used as a natural preservative in processed cheese, milk, dairy products, canned foods, hot baked flour products and pasteurized liquid egg [8]. On the other hand, its use is limited to 15 ppm in meat products by the FDA [9]. Nisin could be added directly to the juices [10,11,12] or incorporated in polymers for controlled release during storage against A. acidoterrestris [13]. Similar to nisin, hen egg white lysozyme has Generally Recognized as Safe (GRAS) status. It has been used as a food preservative in cheeses, cow's milk, beer, fresh fruits and vegetables, fish, meat and wine [8]. Also, lysozyme could inhibit the growth of A. acidoterrestris in solution, incorporated in water-soluble polyvinyl alcohol films or immobilized on polymer films [14]. Due to its safety and high technological stability, it is considered as an ideal food preservative. European Union allergen legistration requires its labeling because of its ability to cause allergies [15].
Temperature is one of the important extrinsic factors that affect the microbial growth and can be easily changed during food processing and storage. Many predictive models have been developed to investigate the growth kinetics under different temperature conditions [16]. To our knowledge, there is no study about the effect of storage temperature on the antimicrobial activities of nisin and lysozyme against A. acidoterrestris in juice. Therefore, the objectives of the present study were to determine the inhibitory effects of nisin and lysozyme against A. acidoterrestris DSM 3922 cells in the apple juice at different storage temperatures (27, 35 and 43 ℃) and finally to estimate the growth kinetic parameters at non-inhibitory doses.
A. acidoterrestris DSM 3922 type strain was kindly provided by Karl Poralla (Deutsche SammLung von Mikroorganismen und Zellkulturen's collection, Braunschweig, Germany). This culture was grown on Bacillus acidoterrestris Agar (pH 4.0, Merck, Germany) for 2 days at 43 ℃, and then stored in 20% glycerol-BAT broth (Döhler, Germany) at –80 ℃ for further analysis.
Concentrated apple juice (70.3° Brix) was kindly provided by ASYA Fruit Juice and Food Ind. Inc. (Isparta, Turkey) and reconstituted to 11.30 °Brix by a refractometer (Mettler Toledo, USA). The presence of Alicyclobacillus spp. contamination in juice samples was determined by membrane filtration method as previously described [17]. The pH of the juice was measured as 3.82 ± 0.01 (Hanna instruments, Hungary).
Lysozyme (≥40, 000 units/mg protein) from hen egg white and nisin from Lactococcus lactis (2.5%, balance sodium chloride and denatured milk solids) were obtained from Sigma Chem. Co. (St Louis, MO, USA).
First, A. acidoterrestris cells were grown overnight on Potato dextrose agar (Difco, BD) at 43 ℃. The colonies were suspended in 10 mL Maximum Recovery Diluent (Oxoid) to obtain a bacterial density of McFarland 1.0 (106 CFU/mL) using a densitometer (Den-1, HVD Life Sciences, Austria). After centrifugation at 16, 000 × g for 5 min, the pellet was dissolved in 10 mL apple juice. Then, 180 μL juice containing antimicrobial (nisin 0–100 IU/mL or lysozyme, 0–100 mg/L) and 20 μL of the bacterial suspension were added into the wells of a flat bottom 96-well plate in duplicates (Corning Costar) for each temperature tested. The plates were incubated individually at 27, 35 or 43 ℃ in a microplate reader (Varioskan® Flash, Thermo, Finland). Inoculated apple juice without antimicrobials was used as control. Absorbance of the well contents was determined at 600 nm. The averages of absorbance values versus time were plotted to form growth curves. The MIC was defined as the lowest concentration required for the inhibition. Experimental growth data were fitted to the Baranyi growth model [18] in DMFit Version 2.1 software (Institute of Food Research, Norwick, UK) to estimate the growth parameters at non-inhibitory doses.
The mean values and standard deviations were calculated by Excel (Microsoft Corp., USA). The fitting of the model to the experimental data was determined by coefficient of determination (R2) calculated by the DMFit 2.1 program. The higher R2 values provide better prediction by the fitted model [18].
Growth inhibition of A. acidoterrestris in apple juice with nisin was independent on storage temperature. MICs were found as 10 IU/mL nisin under all conditions. Since nisin has great stability at high temperatures and low pH, especially at the range of pH 3–4, it has been used to inhibit or control the growth of A. acidoterrestris in highly acidic drinks [11]. The antimicrobial activity of nisin depends on food environment factors such as pH, lipid content, particle size, storage time, and structural uniformity [19]. During storage, antibacterial activity of nisin is increased in high pH foods and at high temperatures [20]. In the related literature, different MIC values have been reported for Alicyclobacillus spp. This may be due to nisin concentration, the characteristics of juice or medium and the tested species [21]. The MICs of nisin were also found lower than those of other studies but it is difficult to compare the obtained results with previous studies because of the use of different organisms, growth and incubation conditions [21].
In another study, Yamazaki et al. (2000) concluded that nisin has inhibitory effect in unclear commercial juices and no effect in clear drinks. They suggested that nisin may bind polyphenols present in unclear juices and growth may be inhibited because of the binding of nisin to some particles present in the unclear apple juice and the synergism between the polyphenols and nisin. In a previous study, cell growth was completely inhibited in the presence of 100 IU/mL nisin in grapefruit, apple and orange juices at 43 ℃ [10]. According to Yamazaki et al. (2000), cell growth was inhibited on agar plates by 1.56 to 25 IU/mL and 25 to 100 IU/mL at pH 3.4 and 4.2, respectively during incubation at 46 ℃.
Storage at lower temperatures caused the use of higher amounts of lysozyme. The activity of lysozyme was increased at higher temperatures. Denatured lysozyme by heating was found to indicate enhanced antimicrobial activity due to the polymerization [22]. In this study, increasing the storage temperature may have improved the enzymatic activity of lysozyme against A. acidoterrestris by lowering the amount needed for inhibition. The MICs were 10, 2.5 and 1.25 mg/L at 27, 35 and 43 ℃, respectively. In the related literature, it was found to exhibit the highest antimicrobial activity against A. acidoterrestris in saline solutions and the addition of lysozyme in laboratory medium resulted in a protective effect [23]. These researchers also found that the MICs of lysozyme towards vegetative cells ranged from 0.1–6 mg/L in acidified malt extract broth. We also found the MICs of lysozyme in the apple juice within this range at 35 ℃ and 43 ℃.
Although the measurement of the absorbance is useful to estimate its growth, it might help to compare the growth rate and lag time under different conditions [24]. Since growth models developed in sterile broth do not always provide reliable predictions of pathogen growth on non-sterile and non-homogenous foods [25], growth studies were achieved in apple juice instead of laboratory medium or model juice to estimate the growth parameters in this study. As seen from Tables 1 and 2, the growth curves fitted to the Baranyi model had high R2 values (≥0.98). The R2 values indicated that fitted models provided good fit to the experimental data.
T (℃) | IU/mL | λ (h) | µ (h–110–4) | R2 |
27 | 1.25 | 25.79 ± 0.56 | 16.98 ± 0.37 | 0.997 |
2.5 | 29.83 ± 3.45 | 14.13 ± 1.67 | 0.997 | |
5.0 | 48.00 ± 1.69 | 18.07 ± 2.59 | 0.990 | |
Control | 22.67 ± 0.59 | 10.13 ± 0.21 | 0.999 | |
35 | 1.25 | 28.06 ± 0.62 | 33.40 ± 0.47 | 0.997 |
2.5 | 31.42 ± 0.25 | 34.11 ± 1.09 | 0.998 | |
5.0 | 36.50 ± 0.79 | 36.90 ± 0.00 | 0.995 | |
Control | 9.91 ± 1.80 | 28.58 ± 2.05 | 0.996 | |
43 | 1.25 | 18.48 ± 0.01 | 51.37 ± 0.00 | 0.983 |
2.5 | 10.1 ± 0.01 | 37.9 ± 0.03 | 0.992 | |
5.0 | 18.5 ± 0.00 | 51.4 ± 1.00 | 0.980 | |
Control | 5.33 ± 0.04 | 33.76 ± 0.37 | 0.990 | |
Values are estimated using an average of replicates obtained from growth curves. λ is lag phase (h); µ is specific growth rate (h–110–4). |
T (℃) | mg/L | λ (h) | µ (h–110–4) | R2 |
27 | 1.25 | 30.53 ± 1.87 | 13.51 ± 0.27 | 0.999 |
2.5 | 43.04 ± 1.46 | 14.41 ± 0.47 | 0.999 | |
5.0 | 51.10 ± 1.33 | 16.52 ± 0.30 | 0.994 | |
Control | 22.67 ± 0.59 | 10.13 ± 0.21 | 0.999 | |
35 | 0.3 | 16.69 ± 0.22 | 22.17 ± 0.04 | 0.989 |
0.6 | 21.11 ± 0.31 | 25.28 ± 0.05 | 0.990 | |
1.25 | 25.71 ± 1.00 | 31.81 ± 0.40 | 0.986 | |
Control | 9.91 ± 1.80 | 28.58 ± 2.05 | 0.996 | |
43 | 0.08 | 7.06 ± 0.00 | 31.94 ± 0.00 | 0.991 |
0.16 | 7.80 ± 0.04 | 31.56 ± 1.01 | 0.992 | |
0.3 | 14.71 ± 0.03 | 36.61 ± 0.90 | 0.996 | |
Control | 5.33 ± 0.04 | 33.76 ± 0.37 | 0.990 | |
Values are estimated using an average of replicates obtained from growth curves. λ is lag phase (h); µ is specific growth rate (h–110–4). |
The estimated lag times decreased and growth rates increased with increasing storage temperature among the controls. The growth was favored at 43 ℃ with the highest growth rate and shortest lag times most probably due to the thermophilic nature of the tested organism. As seen from Table 1, there was a strong correlation between the growth rates and nisin concentrations at 35 ℃ (R2 > 0.91). In general, it is accepted that µ is not influenced by sublethal injuries after conventional preservation treatments and is identical to that of untreated cells. After exposure to some novel technologies such as pulsed electric fields and electron beam irradiation, the growth rate of surviving cells can be changed [6]. In the present study, the growth rates of the treated cells were higher than that of the controls within each temperature (Table 1). The addition of nisin in the apple juice resulted in an extension of lag phase compared to untreated control cells. We observed a relationship between the lag time and nisin concentrations at 27 and 35 ℃ (R2 > 0.83). At the highest non-inhibitory nisin dose, the increase in the lag time was approximately 25, 27 and 13 h at 27 ℃, 35 ℃ and 43 ℃, respectively.
The growth rates in the presence of lysozyme ranged from approximately 13.5 to 16.5, 22.2 to 31.8, and 31.6 to 36.6 × 10–4 h–1 at 27, 35, and 43 ℃, respectively (Table 2). We observed a linear relationship between the rate and lysozyme concentration at 27 ℃ (R2 > 0.94). As the temperature decreased, the effect of lysozyme on the lag phase extension was more pronounced. There was a strong linear relationship between the lag time and lysozyme concentrations at 27 and 35 ℃ (R2 > 0.98). The treatment with 1.25, 2.5 and 5 mg/L lysozyme delayed the lag time approximately 8, 20 and 28 h at 27 ℃, respectively. When the temperature was increased to 43 ℃, the lag time was delayed with approximately 2, 2.5 and 9 h in the apple juice with 0.08, 0.16 and 0.3 mg/mL lysozyme, respectively. To our knowledge, there is only one study about the modeling growth kinetics of A. acidoterrestris in the broth with monolaurin using absorbance data [26]. They found that the Gompertz and Baranyi models were satisfactorily described the growth curves of cells in the presence of monolaurin. According to their results, monolaurin could be used to inhibit the growth and it was effective on cells by delaying the lag phase approximately 8 h and reducing the growth index from 48% to 32–37%.
We observed a significant difference in the amounts of lysozyme for growth inhibition at three temperatures tested. Both nisin and lysozyme were effective to delay lag time and increase growth rate when used at lower amounts. Differences in the antimicrobial action of nisin and lysozyme against A. acidoterrestris could be explained by variations in storage temperature. The obtained results from this study will be useful to inhibit or delay the growth of A. acidoterrestris by combining extrinsic factors such as storage temperature and natural antimicrobials as a hurdle concept to prolong the shelf-life of commercial apple juices.
Authors would like to thank to the members of the Biotechnology and Bioengineering Research and Application Center of Izmir Institute of Technology for absorbance measurements.
All authors declare no conflicts of interest in this paper.
[1] |
Y. Zhang, Test and verification of AES used for image encryption, 3D Res., 9 (2018), 3. doi: 10.1007/s13319-017-0154-7
![]() |
[2] |
G. D. Ye, C. Pan, Y. X. Dong, Y. Shi, X. L. Huang, Image encryption and hiding algorithm based on compressive sensing and random numbers insertion, Signal Process, 172 (2020), 107563. doi: 10.1016/j.sigpro.2020.107563
![]() |
[3] |
L. H. Gong, K. D. Qiu, C. Z. Deng, N. R. Zhou, An image compression and encryption algorithm based on chaotic system and compressive sensing, Opt. Laser Technol., 115 (2019), 257–267. doi: 10.1016/j.optlastec.2019.01.039
![]() |
[4] | G. D. Ye, C. Pan, Y. X. Dong, K. X. Jiao, X. L. Huang, A novel multi-image visually meaningful encryption algorithm based on compressive sensing and Schur decomposition, Transact. Emerg. Telecommun. Technol., 32 (2021), e4071. |
[5] |
Z. J. Liu, Q. Guo, L. Xu, M. A. Ahmad, S. T. Liu, Double image encryption by using iterative random binary encoding in gyrator domains, Opt. Express, 18 (2010), 12033–12043. doi: 10.1364/OE.18.012033
![]() |
[6] |
H. J. Liu, X. Y. Wang, Color image encryption based on one-time keys and robust chaotic maps, Comput. Math. Appl., 59 (2010), 3320–3327. doi: 10.1016/j.camwa.2010.03.017
![]() |
[7] |
X. Y. Wang, L. T. Liu, Y. Q. Zhang, A novel chaotic block image encryption algorithm based on dynamic random growth technique, Opt. Laser. Eng., 66 (2015), 10–18. doi: 10.1016/j.optlaseng.2014.08.005
![]() |
[8] | Y. L. Ma, C. Q. Li, B. Ou, Cryptanalysis of an image block encryption algorithm based on chaotic maps, J. Inf. Secur. Appl., 54 (2020), 102566. |
[9] |
L. F. Liu, S. D. Hao, J. Lin, Z. Wang, X. Y. Hu, S. X. Miao, Image block encryption algorithm based on chaotic maps, IET Signal Process, 12 (2018), 22–30. doi: 10.1049/iet-spr.2016.0584
![]() |
[10] |
W. H. Liu, K. H. Sun, C. X. Zhu, A fast image encryption algorithm based on chaotic map, Opt. Laser. Eng., 84 (2016), 26–36. doi: 10.1016/j.optlaseng.2016.03.019
![]() |
[11] |
Z. Y. Hua, Y. C. Zhou, H. J. Huang, Cosine-transform-based chaotic system for image encryption, Inform. Sci., 480 (2019), 403–419. doi: 10.1016/j.ins.2018.12.048
![]() |
[12] |
M. Alawida, J. S. Teh, A. Samsudin, W. H. Alshoura, An image encryption scheme based on hybridizing digital chaos and finite state machine, Signal Process, 164 (2019), 249–266. doi: 10.1016/j.sigpro.2019.06.013
![]() |
[13] |
H. J. Li, Y. R. Wang, Z. W. Zuo, Chaos-based image encryption algorithm with orbit perturbation and dynamic state variable selection mechanisms, Opt. Laser. Eng., 115 (2019), 197–207. doi: 10.1016/j.optlaseng.2018.12.002
![]() |
[14] |
A. Belazi, A. A. A. El-Latif, A. V. Diaconu, R. Rhouma, S. Belghith, Chaos-based partial image encryption scheme based on linear fractional and lifting wavelet transforms, Opt. Laser. Eng., 88 (2017), 37–50. doi: 10.1016/j.optlaseng.2016.07.010
![]() |
[15] |
M. Kumari, S. Gupta, A. Malik, A superlative image encryption technique based on bit plane using key-based electronic code book, Multimed. Tools Appl., 79 (2020), 33161–33191. doi: 10.1007/s11042-018-6780-0
![]() |
[16] |
K. Shahna, A. Mohamed, A novel image encryption scheme using both pixel level and bit level permutation with chaotic map, Appl. Soft Comput., 90 (2020), 106162. doi: 10.1016/j.asoc.2020.106162
![]() |
[17] |
L. Teng, X. Y. Wang, A bit-level image encryption algorithm based on spatio temporal chaotic system and self-adaptive, Opt. Commun., 285 (2012), 4048–4054. doi: 10.1016/j.optcom.2012.06.004
![]() |
[18] |
X.Y. Wang, H. L. Zhang, A color image encryption with heterogeneous bit-permutation and correlated chaos, Opt. Commun., 342 (2015), 51–60. doi: 10.1016/j.optcom.2014.12.043
![]() |
[19] |
L. Xu, Z. Li, J. Li, W. Hua, A novel bit-level image encryption algorithm based on chaotic maps, Opt. Laser. Eng., 78 (2016), 17–25. doi: 10.1016/j.optlaseng.2015.09.007
![]() |
[20] |
Z. L. Zhu, W. Zhang, K. W. Wong, H. Yu, A chaos-based symmetric image encryption scheme using a bit-level permutation, Inform. Sci., 181 (2011), 1171–1186. doi: 10.1016/j.ins.2010.11.009
![]() |
[21] |
X. L. Chai, Y. R. Chen, L. Broyde, A novel chaos-based image encryption algorithm using DNA sequence operations, Opt. Laser. Eng., 88 (2017), 197–213. doi: 10.1016/j.optlaseng.2016.08.009
![]() |
[22] |
H. J. Liu, X. Y. Wang, A. kadir, Image encryption using DNA complementary rule and chaotic maps, Appl. Soft Comput., 12 (2012), 1457–1466. doi: 10.1016/j.asoc.2012.01.016
![]() |
[23] |
D. Ravichandran, A. S. Banu, B. K. Murthy, V. Balasubramanian, S. Fathima, R. Amirtharajan, An efficient medical image encryption using hybrid DNA computing and chaos in transform domain, Med. Biol. Eng. Comput., 59 (2021), 589–605. doi: 10.1007/s11517-021-02328-8
![]() |
[24] |
X. P. Wei, L. Guo, Q. Zhang, J. X. Zhang, S. G. Lian, A novel color image encryption algorithm based on DNA sequence operation and hyper-chaotic system, J. Syst. Software, 85 (2012), 290–299. doi: 10.1016/j.jss.2011.08.017
![]() |
[25] |
R. Enayatifar, F. G. Guimaraes, P. Siarry, Index-based permutation-diffusion in multiple-image encryption using DNA sequence, Opt. Laser. Eng., 115 (2019), 131–140. doi: 10.1016/j.optlaseng.2018.11.017
![]() |
[26] |
M. Yildirim, DNA encoding for RGB image encryption with memristor based neuron model and chaos phenomenon, Microelectron. J., 104 (2020), 104878. doi: 10.1016/j.mejo.2020.104878
![]() |
[27] |
Q. Zhang, L. Guo, X. P. Wei, Image encryption using DNA addition combining with chaotic maps, Math. Comput. Model., 52 (2010), 2028–2035. doi: 10.1016/j.mcm.2010.06.005
![]() |
[28] |
H. Hermassi, A. Belazi, R. Rhouma, S. M. Belghith, Security analysis of an image encryption algorithm based on a DNA addition combining with chaotic maps, Multimed. Tools Appl., 72 (2014), 2211–2224. doi: 10.1007/s11042-013-1533-6
![]() |
[29] |
S. Q. Zhu, C. X. Zhu, W. H. Wang, A new image encryption algorithm based on chaos and secure hash sha-256, Entropy, 20 (2018), 716. doi: 10.3390/e20090716
![]() |
[30] |
E. E. García-Guerrero, E. Inzunza-González, O. R. López-Bonilla, J. R. Cárdenas-Valdez, E. Tlelo-Cuautle, Randomness improvement of chaotic maps for image encryption in a wireless communication scheme using PIC-microcontroller via Zigbee channels, Chaos Soliton. Fract., 133 (2020), 109646. doi: 10.1016/j.chaos.2020.109646
![]() |
[31] |
E. Rodríguez-Orozco, E. E. García-Guerrero, E. Inzunza-Gonzalez, O. R. López-Bonilla, A. Flores-Vergara, J. R. Cárdenas-Valdez, et al., FPGA-based chaotic cryptosystem by using voice recognition as access key, Electronics, 7 (2018), 414. doi: 10.3390/electronics7120414
![]() |
[32] |
C. Tanougast, Hardware implementation of chaos based cipher: Design of embedded systems for security applications, Chaos-Based Cryptography, 354 (2011), 297–330. doi: 10.1007/978-3-642-20542-2_9
![]() |
[33] |
A. Flores-Vergara, E. E. García-Guerrero, E. Inzunza González, O. R. López-Bonilla, E. Rodrguez-Orozco, J. R. Cárdenas-Valdez, et al., Implementing a chaotic cryptosystem in a 64-bit embedded system by using multiple-precision arithmetic, Nonlinear Dynam., 96 (2019), 497-516. doi: 10.1007/s11071-019-04802-3
![]() |
[34] |
S. F. Yousif, A. J. Abboud, H. Y. Radhi, Robust image encryption with scanning technology, the El-Gamal algorithm and chaos theory, IEEE Access, 8 (2020), 155184–155209. doi: 10.1109/ACCESS.2020.3019216
![]() |
[35] | X. Z. Dong, L. Zhang, X. W. Gao, An efficient FPGA implementation of ECC modular inversion over F256, Proceedings of the 2nd International Conference on Cryptography, Security and Privacy, (2018), 29–33. |
[36] | X. M. Huang, W. Wang, A novel and efficient design for an RSA cryptosystem with a very large key size, IEEE T. Circuits-II, 62 (2015), 972–976. |
[37] |
S. D. Thabah, M. Sonowal, R. U. Ahmed, P. Saha, Fast and area efficient implementation of RSA algorithm, Proceed. Computer Sci., 165 (2019), 525–531. doi: 10.1016/j.procs.2020.01.024
![]() |
[38] | G. C. Marchesan, N. R. Weirich, E. C. Culau, I. I. Weber, F. G. Moraes, E. Carara, et al., Exploring RSA performance up to 4096-bit for fast security processing on a flexible instruction set architecture processor, IEEE International Conference on Electronics, Circuits and Systems (ICECS), (2018), 18420517. |
[39] | T. Adiono, H. Ega, H. Kasan, S. Fuada, S. Harimurti, Full custom design of adaptable montgomery modular multiplier for asymmetric RSA cryptosystem, International Symposium on Intelligent Signal Processing and Communication Systems (ISPACS), (2017), 17524004. |
[40] |
H. Chen, C. Tanougast, Z. J. Liu, B. Y. Hao, Securing color image by using hyperchaotic system in gyrator transform domains, Opt. Quant. Electron., 48(2016), 396. doi: 10.1007/s11082-016-0669-9
![]() |
[41] |
N. Zhu, Y. T. Wang, J. Liu, J. H. Xie, H. Zhang, Optical image encryption based on interference of polarized light, Opt. Express, 17 (2009), 13418–13424. doi: 10.1364/OE.17.013418
![]() |
[42] |
G. D. Ye, K. X. Jiao, H. S. Wu, C. Pan, X. L. Huang, An asymmetric image encryption algorithm based on a fractional-order chaotic system and the RSA public-key cryptosystem, Int. J. Bifurcat. Chaos, 30 (2020), 2050233. doi: 10.1142/S0218127420502338
![]() |
[43] | J. S. Teh, M. Alawida, Y. C. Sii, Implementation and practical problems of chaos-based cryptography revisited, J. Inf. Secur. Appl., 50 (2020), 102421. |
[44] |
T. Wang, M. H. Wang, Hyperchaotic image encryption algorithm based on bit-level permutation and DNA encoding, Opt. Laser Technol., 132 (2020), 106355. doi: 10.1016/j.optlastec.2020.106355
![]() |
[45] | R. S. Ye, Y. T. Xi, Y. L. Ma, A chaotic image encryption scheme using swapping based confusion approach, IEEE international conference on computer communication and the internet, (2016), 16525393. |
[46] |
X. L. Chai, Z. H. Gan, M. H. Zhang, A fast chaos-based image encryption scheme with a novel plain image-related swapping block permutation and block diffusion, Multimed. Tools Appl., 76 (2017), 15561–15585. doi: 10.1007/s11042-016-3858-4
![]() |
[47] |
X. L. Xue, D. S. Zhou, C. J. Zhou, New insights into the existing image encryption algorithms based on DNA coding, PLoS One, 15 (2020), e0241184. doi: 10.1371/journal.pone.0241184
![]() |
1. | Alina Kunicka-Styczyńska, Agnieszka Tyfa, Dariusz Laskowski, Aleksandra Plucińska, Katarzyna Rajkowska, Krystyna Kowal, Clove Oil (Syzygium aromaticum L.) Activity against Alicyclobacillus acidoterrestris Biofilm on Technical Surfaces, 2020, 25, 1420-3049, 3334, 10.3390/molecules25153334 | |
2. | Soisuda Pornpukdeewattana, Aphacha Jindaprasert, Salvatore Massa, Alicyclobacillusspoilage and control - a review, 2020, 60, 1040-8398, 108, 10.1080/10408398.2018.1516190 | |
3. | Aryádina M Ribeiro, Aline D Paiva, Alexandra MO Cruz, Maria CD Vanetti, Sukarno O Ferreira, Hilário C Mantovani, Bovicin HC5 and nisin reduce cell viability and the thermal resistance of Alicyclobacillus acidoterrestris endospores in fruit juices , 2022, 102, 0022-5142, 3994, 10.1002/jsfa.11747 | |
4. | Patra Sourri, Chrysoula C. Tassou, George-John E. Nychas, Efstathios Z. Panagou, Fruit Juice Spoilage by Alicyclobacillus: Detection and Control Methods—A Comprehensive Review, 2022, 11, 2304-8158, 747, 10.3390/foods11050747 |
T (℃) | IU/mL | λ (h) | µ (h–110–4) | R2 |
27 | 1.25 | 25.79 ± 0.56 | 16.98 ± 0.37 | 0.997 |
2.5 | 29.83 ± 3.45 | 14.13 ± 1.67 | 0.997 | |
5.0 | 48.00 ± 1.69 | 18.07 ± 2.59 | 0.990 | |
Control | 22.67 ± 0.59 | 10.13 ± 0.21 | 0.999 | |
35 | 1.25 | 28.06 ± 0.62 | 33.40 ± 0.47 | 0.997 |
2.5 | 31.42 ± 0.25 | 34.11 ± 1.09 | 0.998 | |
5.0 | 36.50 ± 0.79 | 36.90 ± 0.00 | 0.995 | |
Control | 9.91 ± 1.80 | 28.58 ± 2.05 | 0.996 | |
43 | 1.25 | 18.48 ± 0.01 | 51.37 ± 0.00 | 0.983 |
2.5 | 10.1 ± 0.01 | 37.9 ± 0.03 | 0.992 | |
5.0 | 18.5 ± 0.00 | 51.4 ± 1.00 | 0.980 | |
Control | 5.33 ± 0.04 | 33.76 ± 0.37 | 0.990 | |
Values are estimated using an average of replicates obtained from growth curves. λ is lag phase (h); µ is specific growth rate (h–110–4). |
T (℃) | mg/L | λ (h) | µ (h–110–4) | R2 |
27 | 1.25 | 30.53 ± 1.87 | 13.51 ± 0.27 | 0.999 |
2.5 | 43.04 ± 1.46 | 14.41 ± 0.47 | 0.999 | |
5.0 | 51.10 ± 1.33 | 16.52 ± 0.30 | 0.994 | |
Control | 22.67 ± 0.59 | 10.13 ± 0.21 | 0.999 | |
35 | 0.3 | 16.69 ± 0.22 | 22.17 ± 0.04 | 0.989 |
0.6 | 21.11 ± 0.31 | 25.28 ± 0.05 | 0.990 | |
1.25 | 25.71 ± 1.00 | 31.81 ± 0.40 | 0.986 | |
Control | 9.91 ± 1.80 | 28.58 ± 2.05 | 0.996 | |
43 | 0.08 | 7.06 ± 0.00 | 31.94 ± 0.00 | 0.991 |
0.16 | 7.80 ± 0.04 | 31.56 ± 1.01 | 0.992 | |
0.3 | 14.71 ± 0.03 | 36.61 ± 0.90 | 0.996 | |
Control | 5.33 ± 0.04 | 33.76 ± 0.37 | 0.990 | |
Values are estimated using an average of replicates obtained from growth curves. λ is lag phase (h); µ is specific growth rate (h–110–4). |
T (℃) | IU/mL | λ (h) | µ (h–110–4) | R2 |
27 | 1.25 | 25.79 ± 0.56 | 16.98 ± 0.37 | 0.997 |
2.5 | 29.83 ± 3.45 | 14.13 ± 1.67 | 0.997 | |
5.0 | 48.00 ± 1.69 | 18.07 ± 2.59 | 0.990 | |
Control | 22.67 ± 0.59 | 10.13 ± 0.21 | 0.999 | |
35 | 1.25 | 28.06 ± 0.62 | 33.40 ± 0.47 | 0.997 |
2.5 | 31.42 ± 0.25 | 34.11 ± 1.09 | 0.998 | |
5.0 | 36.50 ± 0.79 | 36.90 ± 0.00 | 0.995 | |
Control | 9.91 ± 1.80 | 28.58 ± 2.05 | 0.996 | |
43 | 1.25 | 18.48 ± 0.01 | 51.37 ± 0.00 | 0.983 |
2.5 | 10.1 ± 0.01 | 37.9 ± 0.03 | 0.992 | |
5.0 | 18.5 ± 0.00 | 51.4 ± 1.00 | 0.980 | |
Control | 5.33 ± 0.04 | 33.76 ± 0.37 | 0.990 | |
Values are estimated using an average of replicates obtained from growth curves. λ is lag phase (h); µ is specific growth rate (h–110–4). |
T (℃) | mg/L | λ (h) | µ (h–110–4) | R2 |
27 | 1.25 | 30.53 ± 1.87 | 13.51 ± 0.27 | 0.999 |
2.5 | 43.04 ± 1.46 | 14.41 ± 0.47 | 0.999 | |
5.0 | 51.10 ± 1.33 | 16.52 ± 0.30 | 0.994 | |
Control | 22.67 ± 0.59 | 10.13 ± 0.21 | 0.999 | |
35 | 0.3 | 16.69 ± 0.22 | 22.17 ± 0.04 | 0.989 |
0.6 | 21.11 ± 0.31 | 25.28 ± 0.05 | 0.990 | |
1.25 | 25.71 ± 1.00 | 31.81 ± 0.40 | 0.986 | |
Control | 9.91 ± 1.80 | 28.58 ± 2.05 | 0.996 | |
43 | 0.08 | 7.06 ± 0.00 | 31.94 ± 0.00 | 0.991 |
0.16 | 7.80 ± 0.04 | 31.56 ± 1.01 | 0.992 | |
0.3 | 14.71 ± 0.03 | 36.61 ± 0.90 | 0.996 | |
Control | 5.33 ± 0.04 | 33.76 ± 0.37 | 0.990 | |
Values are estimated using an average of replicates obtained from growth curves. λ is lag phase (h); µ is specific growth rate (h–110–4). |