Agriculture Reference
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enhanced the resistance to pathogen infection. In pears, stem-end decay was reduced af-
ter inoculating the fruit with
B. cinerea
and treating with 0.1
L/L 1-MCP than without
treatment (Spotts et al., 2007). Natural infections caused by
Phacidiopycnis piri
was also
reduced in 1-MCP-treated fruit, and the fruit remained firmer in storage than untreated fruit.
1-MCP increased disease susceptibility of custard apple, mango, papaya (Hofman et al.,
2001), and avocado (Hofman et al., 2001; Adkins et al., 2005; Woolf et al., 2005). Avocado
has an antifungal diene compound that is present in unripe fruit and its level is enhanced
by ethylene (Leikin-Frenkel and Prusky, 1998). Latent infections of
C. gloeosporioides
were inhibited from developing until the level of the diene compound declined during fruit
ripening. 1-MCP treatment of avocado at two stages of maturity prevented further diene
synthesis, but the early-harvested fruit had high initial levels of diene and because of the
inhibitory effect on ripening, 1-MCP decreased decay development. In the later harvest, the
level of diene was lower and decay developed more rapidly in treated fruit than untreated
fruit (Wang et al., 2006).
Most studies on stone fruits found benefits of 1-MCP treatment in reducing decay. In
two plum cultivars, “Fortune” and “Angeleno,” 1-MCP treatment before storage at low
temperature reduced decay caused by
Monilinia laxa
(Menniti et al., 2004). Also, decay
development in apricots was decreased by 1-MCP in a concentration-dependent manner
(Dong et al., 2002). In peaches, decay development after inoculation with
P.expansum
was
slightly reduced by 1-MCP treatment (Liu et al., 2005). Decay of sweet cherries was also
lower in 1-MCP-treated fruit (Mozetic et al., 2006).
μ
7.6 Responses of vegetables
Most of the research on 1-MCP has been concentrated on climacteric fruit. The dearth of
research on fresh vegetables may be due to the fact that many vegetables are consumed
shortly after harvest rather than being stored for extended periods. Some work has been
done on broccoli, carrots, cucumbers, and lettuce. Broccoli is very sensitive to ethylene,
which promotes senescence and yellowing. This is delayed by treatment with 1-MCP (Fan
and Mattheis, 2000a). On the other hand, yellowing of cucumbers was delayed by 1-MCP
only when ethylene was present (Nilsson, 2005). Both Nilsson using cucumbers and Able
et al. (2003) examining bok choy and broccoli found that 1-MCP had to be applied imme-
diately after harvest, otherwise its efficacy was greatly reduced. If cucumbers were stored
before applying 1-MCP, the treatment was ineffective. Apparently, senescent processes are
activated soon after harvest, and once they begin 1-MCP cannot stop their progression.
In carrots and lettuce, treatment with 1-MCP was found to prevent physiological disor-
ders that were associated with ethylene (Fan and Mattheis, 2000b). In carrots, the bitterness
due to accumulation of isocoumarin, and in lettuce, the phenols synthesized through the
shikimic acid pathway leading to russet spotting were prevented. Potatoes close wounds
inflicted during harvesting by developing a layer of suberin, and during this wound healing,
ethylene is produced by the tuber. Preventing the production of ethylene by 1-MCP or other
inhibitors did not affect suberization (Lulai and Suttle, 2004). Onion bulbs responded to 1-
MCP by maintaining higher sugar and dry weight levels (Chope et al., 2007). Sprout growth
was reduced by 1-MCP treatment at 4 and 12
◦
C, but not at 20
◦
C. Germination of chayote
(
Sechium edule
(Jacq.) Sw), a vegetable native to Middle America, was also prevented by
1-MCP (Cadena-Iniguez et al., 2006).
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