Physicochemical Characterization of Crithmum maritimum L. and Daucus carota subsp. gummifer (Syme) Hook.ﬁl. and Their Antimicrobial Activity against Apple Tree and Grapevine Phytopathogens

: Crithmum maritimum and Daucus carota subsp. gummifer are two species of the Apiaceae family that share multiple characteristics: both are halophitic, live on cliffs in the same geographic habitats, and are edible. While C. maritimum is rich in essential oils and ﬂavonoids, D. carota is rich in terpenes and a gum producer. In the work presented herein, the biomass of these two wild plants and the bioactive compounds present in their extracts have been studied by elemental and thermal analysis, infrared spectroscopy, and gas chromatography-mass spectroscopy. To explore their bioactivities, both their hydroalcoholic extracts and their major constituents (apiole in C. maritimum and geranyl acetate in D. carota ), either alone or in combination with chitosan oligomers, were assayed in vitro against bacterial and fungal pathogens that affect apple trees ( Malus domestica ) and grapevine ( Vitis vinifera ). Remarkable inhibition was observed against Erwinia amylovora , the causal agent of ﬁre blight in apple; Xylophilus ampelinus [syn. Erwinia vitivora ], the causal agent of bacterial blight of grapevine; and Diplodia seriata , a virulent pathogen of grapevines that also causes canker, leaf spot and fruit rot of apple. In view of their effectiveness against these three phytopathogens, a potential application of these two medicinal plants in organic farming may be envisaged.


Introduction
Crithmum maritimum L., the sole species of Crithmum genus, is a perennial wild plant that is found on cliffs in southern and western coasts of the British Isles, on western and Mediterranean coasts of Europe, in North Africa and the Canary Islands. It is known as samphire, rock samphire, sea fennel, and, in Asturias (Spain), as cenoyo de mar. It belongs to the Apiaceae family and is an oleaginous halophyte. It has fleshy, divided aromatic leaves, which have a hot and spicy taste (Figure 1). A detailed morphological description, together with a discussion of its eco-physiological responses to salt stress, may be found in the review paper by Atia, et al. [1]. These two medicinal plants have been reported to produce interesting secondary metabolites [3]. Spectrometric analyses of the contents of flavonoids, tannins, and total polyphenols in the aerial parts of rock samphire collected on the Adriatic coast of Croatia in different growth stages were reported by Males, et al. [4], with the highest contents of above components in the samples collected before flowering. Phenolic acids, such as caffeic, chlorogenic, ferulic, p-hydroxybenzoic, p-coumaric vanillic, protocatechuic, and syringic acids were identified by Bartnik, et al. [5]. According to Pavela, et al. [6], the essential oils (EO) of C. maritimum show notable variability in chemical composition, being dominated by dillapiole and γ-terpinene (French EO), limonene and γ-terpinene (central Italy EO), and thymol methyl ether and γ-terpinene (Sicilian EO).
With regard to the potential applications of these bioactive compounds, the antimicrobial activity of the EO of C. maritimum has been assayed against common food-borne bacteria, finding significant inhibition against Escherichia coli, Candida albicans, Listeria innucia, Pseudomonas aeruginosa, Bacillus subtilis, Staphylococcus epidermidis, and Staphylococcus aureus [9,10]. Its antimicrobial activity against a panel of microorganisms, including clinical isolates and food-borne pathogens, has also been studied [11]. The EO obtained from D. carota (albeit not for subsp. gummifer) has been assayed against S. aureus, E. coli, P. aeruginosa, Enterobacter aerogenes, B. subtilis, Campylobacter jejuni, Microsporum canis, and C. albicans by Rossi, et al. [12], Ozcelik, et al. [13], and Pavoni, et al. [14]. Only Valente, et al. [8] and Nawel, et al. [15] explored the EO from D. carota subs. gummifer as a natural source of antifungals against clinical strains of bacteria, yeast, and filamentous fungi.
Nonetheless, to the best of the authors' knowledge, the efficacy of these wild plants extracts has barely been explored against pathogens affecting crop species: C. maritimum Daucus carota subsp. gummifer (Syme) Hook.fil. is also a member of the Apiaceae, and is a herb of maritime cliffs, dunes, and grasslands. It is mostly found on the northern coast of Spain, although it may also be found on southern and western coasts of Britain. The common names of this D. carota subspecies include sea carrot, wild carrot, bird's nest, bishop's lace, and Queen Anne's lace. In Spanish language, it is named zanahoria de acantilado (tr. cliff carrot). It is hairy, with a stiff, solid stem ( Figure 1). The leaves are tripinnate, finely divided, lacy, triangular in shape. Its flowers-small and white, clustered in flat, dense umbels-are sometimes battered and fried. The root is edible while young, but it quickly becomes too woody to consume. The leaves are also edible in little quantities. It contains small amounts of toxicant cyanogenic glycosides [2].
These two medicinal plants have been reported to produce interesting secondary metabolites [3]. Spectrometric analyses of the contents of flavonoids, tannins, and total polyphenols in the aerial parts of rock samphire collected on the Adriatic coast of Croatia in different growth stages were reported by Males, et al. [4], with the highest contents of above components in the samples collected before flowering. Phenolic acids, such as caffeic, chlorogenic, ferulic, p-hydroxybenzoic, p-coumaric vanillic, protocatechuic, and syringic acids were identified by Bartnik, et al. [5]. According to Pavela, et al. [6], the essential oils (EO) of C. maritimum show notable variability in chemical composition, being dominated by dillapiole and γ-terpinene (French EO), limonene and γ-terpinene (central Italy EO), and thymol methyl ether and γ-terpinene (Sicilian EO).
With regard to the potential applications of these bioactive compounds, the antimicrobial activity of the EO of C. maritimum has been assayed against common food-borne bacteria, finding significant inhibition against Escherichia coli, Candida albicans, Listeria innucia, Pseudomonas aeruginosa, Bacillus subtilis, Staphylococcus epidermidis, and Staphylococcus aureus [9,10]. Its antimicrobial activity against a panel of microorganisms, including clinical isolates and food-borne pathogens, has also been studied [11]. The EO obtained from D. carota (albeit not for subsp. gummifer) has been assayed against S. aureus, E. coli, P. aeruginosa, Enterobacter aerogenes, B. subtilis, Campylobacter jejuni, Microsporum canis, and C. albicans by Rossi, et al. [12], Ozcelik, et al. [13], and Pavoni, et al. [14]. Only Valente, et al. [8] and Nawel, et al. [15] explored the EO from D. carota subs. gummifer as a natural source of antifungals against clinical strains of bacteria, yeast, and filamentous fungi.
Nonetheless, to the best of the authors' knowledge, the efficacy of these wild plants extracts has barely been explored against pathogens affecting crop species: C. maritimum EO has only been tested against Erwinia carotovora (which causes beet vascular necrosis, blackleg of potato and other vegetables, and slime flux on various tree species) by Ruberto, et al. [16], and against Mycogone perniciosa (which causes severe crop losses in common mushroom cultivation) by Glamoclija, et al. [17]. In this work, their application to the control of apple tree (Malus domestica Borkh.) and grapevine (Vitis vinifera L.) pathogens, in particular against two bacteria, namely Erwinia amylovora (Burrill) and Xylophilus ampelinus (Panagopoulos, 1969) Willems et al., 1987 [syn. Erwinia vitivora], and a fungus, viz. Diplodia seriata De Not., is evaluated.
Erwinia amylovora is the causal agent of fire blight, a major global threat to commercial apple and pear production [18]. It is cataloged as a quarantine organism in the European Union, and it has been included in the top 10 plant pathogenic bacteria [19]. A panorama of this pathogen's biology, epidemiology, and control may be found in the recent review by Zhao, et al. [20]. X. ampelinus (syn. Xanthomonas ampelina and Erwinia vitivora [21]), the causal agent of bacterial necrosis of grapevines (known as "maladie d'Oléron" in France and "mal nero" in Italy), severely affects grape crops, resulting in harvest losses as high as 70% of typical yield [22]. The European and Mediterranean Plant Protection Organization (EPPO) categorizes X. ampelinus as a quarantine A2 organism, and it is also a quarantine pest for the North American Plant Protection Organization (NAPPO) and the Interafrican Phytosanitary Council (IAPSC). Regarding D. seriata, it is a member of the Botryosphaeriaceae family, which are known to be pathogens, endophytes, and saprophytes on a wide range of woody hosts. D. seriata is a primary and virulent pathogen of grapevines [23,24], but it also causes frog-eye leaf spot, black rot and canker of apples [25][26][27].
Taking into consideration that EU regulation (Article 14 in Directive 2009/128/EC, Council Regulation (EC) 834/2007, Commission Regulation (EC) 889/2008, Regulation (EU) 2019/1009, etc.) promotes the use of formulations based on natural products for Integrated Pest Management (IPM), valorization of these two halophytes from the Asturian coast (Spain) as antimicrobial agents for crop protection is proposed. To explore this possibility, a physicochemical characterization of C. maritimum and D. carota subsp. gummifer is first presented, followed by in vitro studies of the efficacy of their hydromethanolic extracts against the above-referred phytopathogens.

Plant Material and Chemicals
C. maritimum and D. carota subsp. gummifer samples were collected in the cliffs near the beach of San Antolín (Naves, Llanes, Asturias, Spain-43 • 26 32.3 N 4 • 51 59.6 W) in early August, in full flowering. Plant parts from different specimens (n = 10 for each species) were thoroughly mixed to obtain separate composite samples for roots, leaves, stems, and flowers.

Preparation of Plant Extracts
C. maritimum and D. carota subsp. gummifer flowering aerial parts were mixed (1:20, w/v) with a methanol/water solution (1:1 v/v) and heated in a water bath at 50 • C for 30 min, followed by sonication for 5 min in pulse mode with a 1 min stop for each 2.5 min, using a probe-type ultrasonicator model UIP1000hdT (Hielscher Ultrasonics, Teltow, Germany). The solution was then centrifuged at 9000 rpm for 15 min and the supernatant was filtered through Whatman No. 1 paper. Aliquots were lyophilized for CHNS analyses.
The infrared vibrational spectra were registered using a Thermo Scientific (Waltham, MA, USA) Nicolet iS50 Fourier-transform infrared spectrometer, equipped with an in-built diamond attenuated total reflection (ATR) system. The spectra were collected with a 1 cm −1 spectral resolution over the 400-4000 cm −1 range, taking the interferograms that resulted from co-adding 64 scans.
The colorimetric quantification of total polyphenol content (TPC) and total flavonoid content (TFC) was conducted according to the procedures described in [30], using an Agilent (Santa Clara, CA, USA) UV-Vis Cary 100 spectrometer. Contents were expressed in GAE (gallic acid equivalents) and CE (catechin equivalents), respectively. Total carotenoids in D. carota subsp. gummifer were also determined spectrophotometrically, following the methodology described by Garcia Camacho, et al. [31].
The hydroalcoholic plant extracts were studied by gas chromatography-mass spectrometry (GC-MS) at the Research Support Services (STI) at Universidad de Alicante (Alicante, Spain), using a gas chromatograph model 7890A coupled to a quadrupole mass spectrometer model 5975C (both from Agilent Technologies). The chromatographic conditions were: injection volume = 1 µL; injector temperature = 280 • C, in splitless mode; initial oven temperature = 60 • C, 2 min, followed by ramp of 10 • C/min up to a final temperature of 300 • C, 15 min. The chromatographic column used for the separation of the compounds was an Agilent Technologies HP-5MS UI of 30 m length, 0.250 mm diameter, and 0.25 µm film. The mass spectrometer conditions were: temperature of the electron impact source of the mass spectrometer = 230 • C and of the quadrupole = 150 • C; ionization energy = 70 eV. NIST11 library was used for compound identification.

In Vitro Antimicrobial Activity Assessment
The antibacterial activity was assessed according to CLSI standard M07-11 [32], using the agar dilution method to determine the minimum inhibitory concentration (MIC). In short, an isolated colony of E. amylovora in TSB liquid medium was incubated at 30 • C for 18 h. Serial dilutions were then conducted, starting from a 10 8 CFU·mL −1 concentration, to obtain a final inoculum of~10 4 CFU·mL −1 . Bacterial suspensions were then delivered to the surface of PDA plates, to which the bioactive products had previously been added at concentrations ranging from 62.5 to 1500 µg·mL −1 . Plates were incubated at 30 • C for 24 h. In the case of X. ampelinus, the same procedure was followed, albeit at 26 • C. Readings were taken after 24 h. MICs were determined visually in the agar dilutions as the lowest concentrations of the bioactive products at which no bacterial growth was visible. All experiments were run in triplicate, with three 3 plates per treatment/concentration. The antifungal activity of the different treatments was determined using the agar dilution method according to EUCAST standard antifungal susceptibility testing proce-dures [33], by incorporating aliquots of stock solutions onto the PDA medium to obtain concentrations in the 62.5-1500 µg·mL −1 range. Mycelial plugs (∅ = 5 mm), from the margin of 1-week-old PDA cultures of D. seriata, were transferred to plates incorporating the above-mentioned concentrations for each treatment (3 plates per treatment/concentration, with 2 replicates). Plates were incubated at 25 • C in the dark for a week. PDA medium without any amendment was used as the control. Mycelial growth inhibition was estimated according to the formula: ((d c − d t )/d c ) × 100, where d c and d t represent the average diameters of the fungal colony of the control and of the treated fungal colony, respectively. Effective concentrations (EC 50 and EC 90 ) were estimated using PROBIT analysis in IBM SPSS Statistics v.25 (IBM; Armonk, NY, USA) software.
The level of interaction, i.e., synergy factors, were determined according to Wadley's method [34].

Statistical Analysis
The results of the inhibition of mycelial growth of D. seriata as affected by the different concentrations of the treatments were statistically analyzed using one-way analysis of variance (ANOVA), followed by post hoc comparison of means through Tukey's test at p < 0.05. IBM SPSS Statistics v.25 software was used.

Elemental Analysis of Plant Fractions
The C, H, N, and S percentages of C. maritimum components were in the 36.6−40.0%, 6.2-6.3%, 0.7-1.6%, and 0.05-0.1% range, respectively, and those of D. carota subsp. gummifer in the 39.7−42.8%, 6.3−6.4%, 0.6-2.5%, and 0.0-0.3% range, respectively (Table S1). The distribution of N content showed maximum values in the flowering aerial parts, resulting in C/N ratio values noticeably lower than those found for stems and roots. Regarding the elemental analysis of the gels that resulted from the concentration by vacuum evaporation of the hydroalcoholic extracts of the flowering aerial parts of C. maritimum and D. carota subsp. gummifer, presented in Table S2, slightly higher C/N ratios than those reported in Table S1 were observed.

Thermal Characterization of Flowering Aerial Parts
The DSC curve of the flowering aerial parts of C. maritimum ( Figure S1) showed exothermic peaks at 290, 330, and 416 • C, in good correspondence with the exothermal effects associated with xylan and lignin [35]. From the TG curve, the ash content was 2.8%. In the case of the umbel of D. carota subsp. gummifer ( Figure S2), exothermal effects occurred at 323, 402, and 444 • C, and the ash content was 2%.

Vibrational Characterization
The FTIR spectra of the various fractions of C. maritimum (Table S3) showed the specific bands characteristic of oleaginous plants. In particular, the lipid acyl chains absorb at 2916 and 2848 cm −1 , and at 1516 and 1320 cm −1 , while at 1732 cm −1 the ester carbonyl IR response could be observed. The intensity of these bands was in agreement with the high concentrations of oils that this halophyte can store [36].
The spectra from D. carota subsp. gummifer (Table S3) featured three specific bands of carotenes at~1514,~1147, and~1009 cm −1 . The intensity of the bands at 2360 and 2158 cm −1 (attributed to CN stretching) pointed to the presence of appreciable amounts of cyanogen glycosides and anthocyanin. Moreover, the intensity of the amide bands also suggested a significant amount of protein. A notable amount of pectin esters may be inferred from the presence of bands at 2918, 1598, and~808 cm −1 , justifying the ability of this plant to produce gum. With regard to the spectrum from the concentrated gel obtained by evaporation of the hydromethanolic extract of D. carota subsp. gummifer ( Figure S3), the peaks at 2916, 2849, 1732, 1369, 1237, 1144, 1095, and 1015 cm −1 were found to be in good correlation (shifts below 20 cm −1 ) with those of geranyl acetate (2926, 2858, 1742, 1377, 1233, 1163, 1108, and 1024 cm −1 ).

On the Usefulness of the Above Physicochemical Techniques
Valuable information may be retrieved from the elemental analysis data: C/N ratios can shed light on the relative presence of carbohydrates and lipids vs. amines, amides, nitriles, and nitro compounds. Hence, the aerial parts, in which the lowest C/N ratios were registered, are to be used if one would like to obtain a high content of bioactive heterocyclic compounds in the hydroalcoholic extracts.
Infrared spectral fingerprinting is useful to identify and/or fingerprint pectins, proteins, aromatic phenolics, cellulose, hemicellulose, etc. without-in most cases-the need for any physical separation [37]. The Apiaceae dicotyledonous herbs C. maritimum and D. carota are spectroscopically very different from the Gramineae due their higher degree of esterification, which can be crudely assessed by the ratio of the areas of the ester band (at around 1730 cm −1 ) to the polysaccharides band (at 1170-970 cm −1 ). Nevertheless, the spectra of C. maritimum exhibited five specific bands of cellulose (1472 cm −1 , 1320 cm −1 , 1104 cm −1 , 1074 cm −1 , 1034 cm −1 ), and presence of xylan and lignin could also be inferred from the TG-DTG data for C. maritimum. This would support the hypothesis of Abideen, et al. [38], who put forward that the lignocellulosic biomass of this plant could be a potential source of biomass for bioethanol production.
On the other hand, given that the fatty acid methyl ester composition of the oils from C. maritimun and D. carota is comparable to those of other oil crops used for biodiesel production [39], and taking into consideration that their ash contents are not high, their valorization for this application, proposed by Sotiroudis, et al. [36], certainly deserves further attention.
Notwithstanding the above considerations on the utility of thermal and vibrational techniques for plant characterization and applications, they suffer from limitations to identify specific phytochemicals, making it necessary to make use of other more elucidative techniques, such as GC-MS (see below).
For D. carota subsp. gummifer, the total phenolic content (5.0 mg GAE·g −1 ) was lower than those found by Ksouri, et al. [41] for D. carota L. spp. carota extracts (between 7.1 and 13.8 mg GAE·g −1 ). With regard to the amount of carotenoid components in the umbel extract, by our terpene analyses, it was 81 mg β-car/100 g dw, slightly lower than that reported for D. carota leaves (83.5 mg β-car/100 g dw) [42].
The possibility of exploitation of the two studied plants for agricultural chemicals industry applications is supported by above GC-MS results: apiole and dill-apiole, major constituents of C. maritimum, have been shown to be a good insecticide when they were isolated from the roots of Anethum graveolus L. [53], whereas geranyl acetate, the major component of D. carota, has antifungal and anti-inflammatory properties, referred in the studies by Gonçalves, et al. [54] and by Khayyat and Sameeh [55]. Thymol, a phytochemical from C. maritimun, interferes with the formation and viability of hyphae and induces morphological alterations in the envelope (i.e., the plasma membrane and the mannoproteins, enzymes, beta-glucans, and chitin of the wall) of C. albicans, and it also exhibits anti-inflammatory effects by reducing the production and gene expression of the pro-inflammatory mediators [56]. Falcarinol has also been identified as an important

Antibacterial Activity
The inhibition of both C. maritimum and D. carota extracts against Erwinia amylovora and Xylophilus ampelinus were similar (Table 3), although it was slightly higher against X. ampelinus in the case of C. maritimum. As regards the activities of the two main active principles, viz. pure apiole (an essential oil) and pure geranyl acetate (a monoterpene), the obtained results were comparable to or lower than those of the plant extracts. Another was the case for the conjugate complexes, in which a synergistic behavior was observed among COS and the phytochemicals in all cases. The best results against E. amylovora were attained with the COS-C. maritimum complex (MIC = 187.5 µg·mL −1 ), while against X. ampelinus the lowest MIC (125 µg·mL −1 ) corresponded to the COS-geranyl acetate complex, followed by the COS-C. maritimum complex (MIC = 250 µg·mL −1 ).
The above results of antibacterial effect of chitosan-phytochemical conjugates against Erwinia spp. were in accordance with the previous reports [58,59], in which the chitosanphytochemical conjugates exhibited higher antimicrobial activity than that of unmodified chitosan. For instance, Kim, et al. [60] reported that the MICs of chitosan-phytochemical conjugates ranged from 32 to 512 µg·mL −1 against foodborne pathogens, while the MICs of the unmodified chitosan were in the 128−1024 µg·mL −1 range.
In line with Kim, et al. [60], it may be speculated that the mechanism of action behind this enhanced behavior operates via multiple mechanisms: positively charged chitosan can interact with the negatively charged bacterial cell surface, which leads to a weakening of the cell wall, either by cell wall damage alone or accompanied by cell lysis. Conjugation with phytochemicals may increase the osmotic pressure-induced disruption and shrinkage of the bacterial membrane because of a reduction in the permeability of the membrane to intracellular components, and the conjugates may also form a barrier on the bacterial surface and prevent the entry of nutrients. It may also be hypothesized that conjugation with phytochemicals increases the affinity of chitosan for the bacterial cell envelope because of an enhanced lipophilicity (conferred-in the case of apiol-by the allyl side chain bonded to the aromatic ring; and, in the case of geranyl acetate, by the presence of two double bonds in the unsaturated chain). In any case, it should be taken into consideration that further research is required to support aforementioned hypotheses.

Antifungal Activity
Diplodia seriata mycelial growth inhibition results are presented in Figure 2 and Figrue S6. The preconized antifungal activity of D. carota [8], based on its relatively high content of terpenes, was not observed in our assays. That of C. maritimum was also low, with EC 50 and EC 90 values of 832 and 2933 µg·mL −1 , respectively. Even when its main component, apiole (whose antifungal effect has been referred to the presence of two methoxyl groups in positions 2, 3 of their benzene ring, optimum to gain a correct balance of hydrophilicitylipophilicity [61]), was assayed as a pure substance, the results were moderate, with EC 50 and EC 90 values of 333 and 822 µg·mL −1 , respectively.
These results are in line with the low activity of D. carota EO against certain Candida spp. and Aspergillus spp. reported by Valente, et al. [8], and with the lack of activity of apiole against C. acutatum, C. fragariae, C. gloeosporioides, and F. oxysporium reported by Meepagala, et al. [62].
Another was the case for geranyl acetate, the main component of D. carota: when it was assayed as a pure substance, it led to EC 50 and EC 90 values as low as 147 and 172 µg·mL −1 , respectively.
Regarding the activity of the conjugate complexes with COS, an enhancement in the antifungal activity was registered in all cases. The lowest EC 50 and EC 90 values were obtained for COS-geranyl acetate (68 and 113 µg·mL −1 , respectively) and for COS-C. maritimum extract (75 and 331 µg·mL −1 , respectively), for which a synergy factor above 5 was obtained (Table 4).
These results are in line with the low activity of D. carota EO against certain Candida spp. and Aspergillus spp. reported by Valente, et al. [8], and with the lack of activity of apiole against C. acutatum, C. fragariae, C. gloeosporioides, and F. oxysporium reported by Meepagala, et al. [62].
Another was the case for geranyl acetate, the main component of D. carota: when it was assayed as a pure substance, it led to EC50 and EC90 values as low as 147 and 172 µ g·mL −1 , respectively.
Regarding the activity of the conjugate complexes with COS, an enhancement in the antifungal activity was registered in all cases. The lowest EC50 and EC90 values were obtained for COS-geranyl acetate (68 and 113 µ g·mL −1 , respectively) and for COS-C. maritimum extract (75 and 331 µ g·mL −1 , respectively), for which a synergy factor above 5 was obtained (Table 4).    The molecular mechanisms behind chitosan interactions with fungi have been recently discussed in a review paper by Lopez-Moya, et al. [63]. Nonetheless, the information available on the mechanism of synergistic action of COS-phytochemical conjugates is not well-established yet. It has been hypothesized that it may be the result of an enhanced additive fungicidal effect per se, and/or via a concurrent action on diverse fungal metabolic sites. The conjugation with phytochemicals may increase the cationic surface charge of COS, enhancing the linkage (through electrostatic interactions) to the negatively charged site-specific binding receptors on the fungal membrane [28,[64][65][66].

Comparison with Efficacies Reported in the Literature
Results from studies on the antimicrobial activity of the specific bioactive substances under study (C. maritimum and D. carota extracts, apiol, and geranyl acetate) against diverse foodborne and clinical bacteria and fungi are summarized in Table 5. The reported MICs and IC 50 values are generally lower than those reported herein (in this work, the lowest MIC values were 125 and 187.5 µg·mL −1 against X. ampelinus and E. amylovora, respectively, and the lowest EC 50 and EC 90 values against D. seriata were 68 and 113 µg·mL −1 , respec-tively), but it is worth noting that there are certain pathogens for which no inhibition could be attained, and that there is a large variability in the reported values depending on the bioactive product (and its provenance) and even as a function of the strain/isolate for the same pathogen. A comparison with the values reported for other phytopathogens was not possible, given that no inhibition could be attained using a hexane extract of C. maritimum leaves against Erwinia carotovara subsp. carotovora, and the minimum inhibitory quantity (MIQ = 1 µL/disc) reported using C. maritimum roots essential oil against Mycogone perniciosa was not expressed in standard units.
A comparison can instead be made with the efficacy of other natural products reported in the literature against the actual phytopathogens under study. To the best of the authors' knowledge, no assays with plant-derived products have been conducted against X. ampelinus, but E. amylovora has the subject of several studies, summarized in Table 6. In this work, the lowest MIC value against E. amylovora was 187.5 µg·mL −1 , better than those attained with the extracts from Damask rose and golden wreath wattle flowers, Conocarpus lancifolius leaves and different phenolic extracts from clove, oregano, artichoke, or walnut shells. Nonetheless, lower MICs have been reported for the resinous exudates from Adesmia boronioides and alkaloids from African rue seeds.  In relation to the antifungal activity against D. seriata, the lowest EC 50 and EC 90 values for the products assayed herein were 68 and 113 µg·mL −1 , respectively. These were substantially lower than those attained with other natural compounds. For instance, a concentration of 1000 µg·mL −1 was required to completely inhibit the mycelial growth of D. seriata for chitosan oligosaccharides (molecular weight < 3000 Da) [80]; and only 96.8% growth inhibition was reached for chitosan at 25 mg·mL −1 [80]. Growth inhibition percentages of 20.6, 90.5, 47.7, 68.2, and 77.8% were reported by Cobos, et al. [80] for Evernia prunastri lichen extract (4%), garlic extract (10%), lemon peel extract (10%), propolis (10 mg·mL −1 ), and vanillin (5 mg·mL −1 ), respectively. If COS-conjugate complexes are considered instead, the EC 90 values attained with a COS-ε-polylysine conjugate (580 µg·mL −1 ) [28], and a COS-tyrosine conjugate (672 µg·mL −1 ) [65] were substantially higher than those obtained for COS-geranyl acetate and COS-C. maritimum extract, and comparable to those of COS-apiol and COS-D. carota subsp. gummifer extract.

Conclusions
The hydromethanolic extract of the aerial parts of C. maritimum was found to be rich in apiole (55%) and that of D. carota in geranyl acetate (40%). In the in vitro assays, a strong synergistic behavior was observed upon conjugation of the bioactive constituents of plant extracts with chitosan oligosaccharides, with synergy factors in the 3.9-5.1 range. For the COS-C. maritimum complex, MIC values of 187.5 and 250 µg·mL −1 were obtained against E. amylovora and X. ampelinus, respectively; and EC 50 and EC 90 values of 75 and 331 µg·mL −1 were found against D. seriata. For COS-D. carota extract, a MIC value of 375 µg·mL −1 was observed against the two bacterial phytopathogens; and an EC 90 of 633 µg·mL −1 was attained against D. seriata. Taking into consideration that the conjugate complexes of both halophyte extracts showed a better performance than other natural compounds reported in the literature against E. amylovora and D. seriata, they may be put forward as promising antimicrobial treatments, either in organic agriculture or as a substitute for treatments based on chemical synthesis fungicides in conventional management.

Institutional Review Board Statement: Not applicable.
Informed Consent Statement: Not applicable.

Data Availability Statement:
The data presented in this study are available on request from the corresponding author. The data are not publicly available due to their relevance to be part of an ongoing Ph.D. Thesis.